HOUSE DUST - house dust injection, solution 
ALMOND - almond injection, solution 
APPLE - apple injection, solution 
APRICOT - apricot injection, solution 
ASPARAGUS - asparagus injection, solution 
AVOCADO - avocado injection, solution 
BANANA - banana injection, solution 
BARLEY - barley injection, solution 
BEAN - bean injection, solution 
STRING BEAN - string bean injection, solution 
BEEF - beef injection, solution 
BRAZIL NUT - brazil nut injection, solution 
BROCCOLI - broccoli injection, solution 
BUCKWHEAT - buckwheat injection, solution 
CABBAGE - cabbage injection, solution 
CANTALOUPE - cantaloupe injection, solution 
CARROT - carrot injection, solution 
CASEIN - casein injection, solution 
CELERY - celery injection, solution 
CHERRY - cherry injection, solution 
CHICKEN - chicken injection, solution 
CINNAMON - cinnamon injection, solution 
CLAM - clam injection, solution 
COCOA BEAN - cocoa bean injection, solution 
COCONUT - coconut injection, solution 
CODFISH - codfish injection, solution 
COFFEE BEAN - coffee bean injection, solution 
CRAB - crab injection, solution 
CUCUMBER - cucumber injection, solution 
EGG WHITE - egg white injection, solution 
EGG - egg injection, solution 
EGG YOLK - egg yolk injection, solution 
FLOUNDER - flounder injection, solution 
GARLIC - garlic injection, solution 
GRAPE - grape injection, solution 
GRAPEFRUIT - grapefruit injection, solution 
KARAYA GUM - karaya gum injection, solution 
HONEYDEW MELON - honeydew melon injection, solution 
LAMB - lamb injection, solution 
LEMON - lemon injection, solution 
LETTUCE - lettuce injection, solution 
LIMA BEAN - lima bean injection, solution 
LOBSTER - lobster injection, solution 
GOAT MILK - goat milk injection, solution 
COW MILK - cow milk injection, solution 
MUSHROOM - cultivated mushroom injection, solution 
MUSTARD SEED - mustard seed injection, solution 
OAT - oat injection, solution 
BLACK OLIVE - black olive injection, solution 
ONION - onion injection, solution 
ORANGE - orange injection, solution 
OYSTER - oyster injection, solution 
PEA - pea injection, solution 
PEACH - peach injection, solution 
PEANUT - peanut injection, solution 
PEAR - pear injection, solution 
PECAN - pecan injection, solution 
GREEN BELL PEPPER - green bell pepper injection, solution 
PEPPER - pepper injection, solution 
PINEAPPLE - pineapple injection, solution 
PISTACHIO - pistachio injection, solution 
PLUM - plum injection, solution 
PORK - pork injection, solution 
POTATO - potato injection, solution 
POTATO - potato injection, solution 
RICE - rice injection, solution 
RYE - rye injection, solution 
SALMON - salmon injection, solution 
SESAME SEED - sesame seed injection, solution 
SHRIMP - shrimp injection, solution 
SOYBEAN - soybean injection, solution 
SPINACH - spinach injection, solution 
SQUASH - squash injection, solution 
STRAWBERRY - strawberry injection, solution 
CORN - corn injection, solution 
TOMATO - tomato injection, solution 
TUNA - tuna injection, solution 
TURKEY - turkey injection, solution 
VANILLA - vanilla injection, solution 
ENGLISH WALNUT - english walnut injection, solution 
WATERMELON - watermelon injection, solution 
WHEAT - wheat injection, solution 
BOS TAURUS SKIN - bos taurus skin injection, solution 
COTTON FIBER - cotton fiber injection, solution 
COTTON SEED - cotton seed injection, solution 
CANIS LUPUS FAMILIARIS SKIN - canis lupus familiaris skin injection, solution 
CAVIA PORCELLUS SKIN - cavia porcellus skin injection, solution 
EQUUS CABALLUS SKIN - equus caballus skin injection, solution 
CEIBA PENTANDRA FIBER - ceiba pentandra fiber injection, solution 
MUS MUSCULUS SKIN - mus musculus skin injection, solution 
ORRIS - orris injection, solution 
PYRETHRUM CINERARIIFOLIUM - pyrethrum cinerariifolium injection, solution 
RABBIT - rabbit injection, solution 
SOLENOPSIS INVICTA - solenopsis invicta injection, solution 
PERIPLANETA AMERICANA - periplaneta americana injection, solution 
BLATELLA GERMANICA - blatella germanica injection, solution 
ACREMONIUM STRICTUM - acremonium strictum injection, solution 
ALTERNARIA TENUIS - alternaria alternata injection, solution 
ASPERGILLUS FUMIGATUS - aspergillus fumigatus injection, solution 
ASPERGILLUS NIGER VAR. NIGER - aspergillus niger var. niger injection, solution 
AUREOBASIDIUM PULLULANS VAR. PULLULANS - aureobasidium pullulans var. pullutans injection, solution 
BOTRYTIS CINEREA - botrytis cinerea injection, solution 
CANDIDA ALBICANS - candida albicans injection, solution 
CHAETOMIUM GLOBOSUM - chaetomium globosum injection, solution 
CLADOSPORIUM CLADOSPORIOIDES - cladosporium cladosporioides injection, solution 
CLADOSPORIUM SPHAEROSPERMUM - cladosporium sphaerospermum injection, solution 
COCHLIOBOLUS SATIVUS - cochliobolus sativus injection, solution 
EPICOCCUM NIGRUM - epicoccum nigrum injection, solution 
FUSARIUM OXYSPORUM VASINFECTUM - fusarium oxysporum vasinfectum injection, solution 
HELMINTHOSPORIUM SOLANI - helminthosporium solani injection, solution 
MUCOR PLUMBEUS - mucor plumbeus injection, solution 
NEUROSPORA INTERMEDIA - neurospora intermedia injection, solution 
KHUSKIA ORYZAE - khuskia oryzae injection, solution 
PHOMA EXIGUA VAR. EXIGUA - phoma exigua var. exigua injection, solution 
RHIZOPUS ARRHIZUS VAR. ARRHIZUS - rhizopus arrhizus var. arrhizus injection, solution 
RHODOTORULA RUBRA - rhodotorula rubra injection, solution 
USTILAGO MAYDIS - ustilago maydis injection, solution 
USTILAGO TRITICI - ustilago tritici injection, solution 
STEMPHYLIUM SOLANI - stemphylium solani injection, solution 
TRICHOPHYTON MENTAGROPHYTES - trichophyton mentagrophytes injection, solution 
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM - penicillium chrysogenum var. chrysogenum injection, solution 
ACACIA - acacia injection, solution 
ALNUS INCANA SSP. RUGOSA POLLEN - alnus incana subsp. rugosa pollen injection, solution 
MEDICAGO SATIVA POLLEN - medicago sativa pollen injection, solution 
FRAXINUS AMERICANA POLLEN - fraxinus americana pollen injection, solution 
PASPALUM NOTATUM POLLEN - paspalum notatum pollen injection, solution 
MORELLA CERIFERA POLLEN - morella cerifera pollen injection, solution 
FAGUS GRANDIFOLIA POLLEN - fagus grandifolia pollen injection, solution 
BETULA LENTA POLLEN - betula lenta pollen injection, solution 
BETULA NIGRA POLLEN - betula nigra pollen injection, solution 
BETULA LENTA POLLEN - betula lenta pollen injection, solution 
ACER NEGUNDO POLLEN - acer negundo pollen injection, solution 
AMARANTHUS PALMERI POLLEN - amaranthus palmeri pollen injection, solution 
JUNIPERUS ASHEI POLLEN - juniperus ashei pollen injection, solution 
JUNIPERUS VIRGINIANA POLLEN - juniperus virginiana pollen injection, solution 
XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN - xanthium strumarium var. canadense pollen injection, solution 
POPULUS DELTOIDES POLLEN - populus deltoides pollen injection, solution 
CUPRESSUS ARIZONICA POLLEN - cupressus arizonica pollen injection, solution 
TAXODIUM DISTICHUM POLLEN - taxodium distichum pollen injection, solution 
RUMEX ACETOSELLA POLLEN - rumex acetosella pollen injection, solution 
RUMEX CRISPUS POLLEN - rumex crispus pollen injection, solution 
ULMUS AMERICANA POLLEN - ulmus americana pollen injection, solution 
SOLIDAGO CANADENSIS POLLEN - solidago canadensis pollen injection, solution 
CELTIS OCCIDENTALIS POLLEN - celtis occidentalis pollen injection, solution 
CARYA OVATA POLLEN - carya ovata pollen injection, solution 
SORGHUM HALEPENSE POLLEN - sorghum halepense pollen injection, solution 
JUNIPERUS CALIFORNICA POLLEN - juniperus californica pollen injection, solution 
KOCHIA SCOPARIA POLLEN - kochia scoparia pollen injection, solution 
CHENOPODIUM ALBUM POLLEN - chenopodium album pollen injection, solution 
ACER RUBRUM POLLEN - acer rubrum pollen injection, solution 
ACER SACCHARUM POLLEN - acer saccharum pollen injection, solution 
IVA XANTHIFOLIA POLLEN - iva xanthifolia pollen injection, solution 
IVA ANNUA VAR. ANNUA POLLEN - iva annua var. annua pollen injection, solution 
PROSOPIS JULIFLORA POLLEN - prosopis juliflora pollen injection, solution 
ARTEMISIA VULGARIS POLLEN - artemisia vulgaris pollen injection, solution 
MORUS RUBRA POLLEN - morus rubra pollen injection, solution 
MORUS ALBA POLLEN - morus alba pollen injection, solution 
QUERCUS RUBRA POLLEN - quercus rubra pollen injection, solution 
QUERCUS VIRGINIANA POLLEN - quercus virginiana pollen injection, solution 
QUERCUS ALBA POLLEN - quercus alba pollen injection, solution 
OLEA EUROPAEA POLLEN - olea europaea pollen injection, solution 
SYAGRUS ROMANZOFFIANA POLLEN - syagrus romanzoffiana pollen injection, solution 
CARYA ILLINOINENSIS POLLEN - carya illinoinensis pollen injection, solution 
AMARANTHUS RETROFLEXUS POLLEN - amaranthus retroflexus pollen injection, solution 
PINUS STROBUS POLLEN - pinus strobus pollen injection, solution 
PLANTAGO LANCEOLATA POLLEN - plantago lanceolata pollen injection, solution 
POPULUS ALBA POLLEN - populus alba pollen injection, solution 
LIGUSTRUM VULGARE POLLEN - ligustrum vulgare pollen injection, solution 
ELYMUS REPENS POLLEN - elymus repens pollen injection, solution 
AMBROSIA TRIFIDA POLLEN - ambrosia trifida pollen injection, solution 
SALSOLA KALI POLLEN - salsola kali pollen injection, solution 
ARTEMISIA TRIDENTATA POLLEN - artemisia tridentata pollen injection, solution 
LIQUIDAMBAR STYRACIFLUA POLLEN - liquidambar styraciflua pollen injection, solution 
PLATANUS OCCIDENTALIS POLLEN - platanus occidentalis pollen injection, solution 
JUGLANS NIGRA POLLEN - juglans nigra pollen injection, solution 
AILANTHUS ALTISSIMA POLLEN - ailanthus altissima pollen injection, solution 
POPULUS TREMULOIDES POLLEN - populus tremuloides pollen injection, solution 
POA ANNUA POLLEN - poa annua pollen injection, solution 
BROMUS INERMIS POLLEN - bromus inermis pollen injection, solution 
ZEA MAYS POLLEN - zea mays pollen injection, solution 
POPULUS FREMONTII POLLEN - populus fremontii pollen injection, solution 
POPULUS DELTOIDES SSP. MONILIFERA POLLEN - populus deltoides subsp. monilifera pollen injection, solution 
EUPATORIUM CAPILLIFOLIUM POLLEN - eupatorium capillifolium pollen injection, solution 
ULMUS CRASSIFOLIA POLLEN - ulmus crassifolia pollen injection, solution 
ULMUS PUMILA POLLEN - ulmus pumila pollen injection, solution 
EUCALYPTUS GLOBULUS POLLEN - eucalyptus globulus pollen injection, solution 
CORYLUS AMERICANA POLLEN - corylus americana pollen injection, solution 
ROBINIA PSEUDOACACIA POLLEN - robinia pseudoacacia pollen injection, solution 
MELALEUCA QUINQUENERVIA POLLEN - melaleuca quinquenervia pollen injection, solution 
CHENOPODIUM AMBROSIOIDES POLLEN - chenopodium ambrosioides pollen injection, solution 
QUERCUS AGRIFOLIA POLLEN - quercus agrifolia pollen injection, solution 
QUERCUS ALBA POLLEN - quercus alba pollen injection, solution 
SCHINUS MOLLE POLLEN - schinus molle pollen injection, solution 
AMARANTHUS SPINOSUS POLLEN - amaranthus spinosus pollen injection, solution 
CASUARINA EQUISETIFOLIA POLLEN - casuarina equisetifolia pollen injection, solution 
PINUS ECHINATA POLLEN - pinus echinata pollen injection, solution 
AMBROSIA ACANTHICARPA POLLEN - ambrosia acanthicarpa pollen injection, solution 
AMBROSIA TENUIFOLIA POLLEN - ambrosia tenuifolia pollen injection, solution 
AMBROSIA BIDENTATA POLLEN - ambrosia bidentata pollen injection, solution 
AMBROSIA PSILOSTACHYA POLLEN - ambrosia psilostachya pollen injection, solution 
LOLIUM PERENNE SSP. MULTIFLORUM POLLEN - lolium perenne ssp. multiflorum pollen injection, solution 
ARTEMISIA FRIGIDA POLLEN - artemisia frigida pollen injection, solution 
DISTICHLIS SPICATA POLLEN - distichlis spicata pollen injection, solution 
HOLCUS LANATUS POLLEN - holcus lanatus pollen injection, solution 
JUGLANS NIGRA POLLEN - juglans nigra pollen injection, solution 
JUGLANS REGIA POLLEN - juglans regia pollen injection, solution 
TRITICUM AESTIVUM POLLEN - triticum aestivum pollen injection, solution 
ARTEMISIA ANNUA POLLEN - artemisia annua pollen injection, solution 
AMARANTHUS TUBERCULATUS POLLEN - amaranthus tuberculatus pollen injection, solution 
COTTON FIBER - cotton fiber injection, solution 
ACREMONIUM STRICTUM - acremonium strictum injection, solution 
AUREOBASIDIUM PULLULANS VAR. PULLULANS - aureobasidium pullulans var. pullutans injection, solution 
COCHLIOBOLUS SATIVUS - cochliobolus sativus injection, solution 
MUCOR PLUMBEUS - mucor plumbeus injection, solution 
SACCHAROMYCES CEREVISIAE - saccharomyces cerevisiae injection, solution 
FRAXINUS VELUTINA POLLEN - fraxinus velutina pollen injection, solution 
LIQUIDAMBAR STYRACIFLUA POLLEN - liquidambar styraciflua pollen injection, solution 
SALIX NIGRA POLLEN - salix nigra pollen injection, solution 
ALK-Abello, Inc.

----------

Allergenic Extracts For Diagnostic Use Only

ALLERGENIC EXTRACTS, FOR DIAGNOSTIC USE ONLY

DIRECTIONS FOR USE

WARNINGS

This product is intended for use by physicians who are experienced in the administration of allergenic extracts and the emergency care of anaphylaxis, or for use under the guidance of an allergy specialist.

As with all allergenic extracts, severe systemic reactions may occur. In certain individuals these life-threatening reactions may result in death. Fatalities associated with skin testing have been reported. Patients should be observed for at least 20 - 30 minutes following testing. Emergency measures and adequately trained personnel should be immediately available in the event of a life-threatening reaction.

Patients with unstable asthma or steroid dependent asthmatics and patients with underlying cardiovascular disease are at greater risk to a fatal outcome from a systemic allergic reaction.

Sensitive patients may experience severe anaphylactic reactions resulting in respiratory obstruction, shock, coma and/or death. Adverse events are to be reported to MedWatch (1-800-FDA-1088), Adverse Experience Reporting, HFM-210 Center for Biologics Evaluation & Research, Food and Drug Administration, 1401 Rockville Pike, Rockville, MD 20852-1448.

This product should not be injected intravenously. Patients receiving beta blockers may not be responsive to epinephrine or inhaled bronchodilators. Respiratory obstruction not responding to parenteral or inhaled bronchodilators may require theophylline, oxygen, intubation and the use of life support systems. Parenteral fluid and/or plasma expanders may be utilized for the treatment of shock. Adrenocorticosteroids may be administered parenterally or intravenously.

Refer to WARNINGS, PRECAUTIONS, and ADVERSE REACTIONS sections below.

                 

 

DESCRIPTION

Sterile diagnostic extracts are supplied in either phenol-saline diluent for Intradermal Testing or in diluent containing glycerin 50% (v/v) for Percutaneous Testing and phenol 0.4% (preservative). Inactive ingredients may include: sodium chloride for isotonicity, glycerin, and sodium bicarbonate as a buffer. Inactive ingredients in mold extracts may include residual potassium phosphate, and calcium carbonate from growth media.

Pollens are individually extracted from pure pollen extracted in a phenol-preserved sodium bicarbonate solution. Short Ragweed and Mixed (Tall and Short) Ragweed extracts are standardized by Antigen E content and so labeled. The Antigen E content of extracts containing Short Ragweed at a concentration more dilute than a weight/volume ratio of 1:10 are obtained by calculating the Antigen E content based on the assay value of more concentrated extract. Pollen extracts are filtered aseptically and after final packaging, they are tested for sterility and safety.

House Dust, a heterogenous, widely distributed allergen, is among the most frequently encountered as a primary or accompanying cause of allergic symptoms. Allergic inhalants found in house dust include mites, insects, mold spores, feathers, animal dander, pollens, hairs, food and cleansing agent residues. Individual environs may contain certain items not ordinarily found so that a stock house dust extract may not elicit a response on testing. House Dust Extracts are prepared from dust collected from homes and from establishments which clean household rugs. It is extracted from buffered, aqueous extracting fluid. House Dust Extract is dialyzed, filtered aseptically, and after final packaging is tested for sterility and safety.

Molds (fungi) are present in all inhabited places at all seasons of the year; they are so ubiquitous that they are prevalent at times when common allergic pollens and other inhalants are not. In the home and surroundings, molds are found in upholstered furniture, mattresses, drapes, cellar and storage room dust, woolens, leather goods, fruits, meats, cheeses, garden soil and on plants. Spores, mycelial fragments and mold residues are thus inhaled, contacted and ingested continuously. Mold extracts are extracted in a phenol preserved saline solution. The extract is dialyzed, filtered aseptically and after final packaging is tested for sterility and safety.

Foods, miscellaneous inhalants and epidermals are individually extracted in phenol preserved saline, filtered aseptically and after final packaging are tested for sterility and safety.

CLINICAL PHARMACOLOGY

Diagnostically (for skin testing), the allergen combines with IgE antibodies fixed to mast cells in the skin. This complexing causes an increase in cellular permeability and degranulation of the mast cells releasing chemical mediators. These mediators (such as histamine) are responsible for a local inflammatory response of wheal and erythema typical of a positive skin test reaction and also, the symptoms commonly associated with allergic disease.1 The more mediator release, the larger the reaction (wheal and erythema).

INDICATIONS AND USAGE

These products are for diagnostic use only. Diagnostic allergenic extracts are indicated for use in skin testing to establish the clinical relevance of specific allergens to which the patient has been exposed. By measuring skin test response the physician may assess the degree of sensitivity that patients have to the allergens. For extracts standardized in AU and BAU, see individual directions for use.  Allergenic extracts for diagnostic use only of coffee, mosquito, cottonseed, and flaxseed have not been shown by adequate data to be safe and effective for therapeutic use.

CONTRAINDICATIONS

Patients on beta blockers can be non-responsive to beta agonists that may be required to reverse a systemic reaction (also, see boxed WARNINGS statement and ADVERSE REACTIONS). The physician should carefully weigh the benefit derived from skin testing vs. the risk to the patient should a systemic reaction arise.

Patients with unstable asthma or steroid dependent asthmatics and patients with underlying cardiovascular disease are at greater risk to a fatal outcome from a systemic allergic reaction2, 3. See also PRECAUTIONS and ADVERSE REACTIONS.

WARNINGS

Patients should always be observed for at least 20 - 30 minutes after skin testing. In the event of a marked systemic reaction such as urticaria, angioedema, wheezing, dyspnea, respiratory obstruction, hypotension, coma and death (see ADVERSE REACTIONS), applications of a tourniquet above the injection site and administration of 0.2 mL to 1 mL (0.01 mg/kg) of epinephrine injection (1:1,000) are recommended. Maximal recommended dose for children between 2 and 12 years of age is 0.5 mL. The tourniquet is then gradually released at 15 minute intervals. Patients under treatment with beta blockers may be refractory to the usual dose of epinephrine.

Volume expanders and vasopressor agents may be required to reverse hypotension, inhalation bronchodilators and parenteral aminophylline may be required to reverse bronchospasm. In case of respiratory obstruction, oxygen and intubation may be necessary. Life-threatening reactions unresponsive to the above may require cardiopulmonary resuscitation.

PRECAUTIONS

INFORMATION FOR PATIENTS:

Patients should be instructed to describe any active allergic symptoms such as rhinitis, wheezing, dyspnea, etc. prior to testing. Also, see ADVERSE REACTIONS and WARNINGS Sections.

Patients should always be observed 20 to 30 minutes after testing.

General:

  1. In the presence of active symptoms such as rhinitis, wheezing, dyspnea, etc., the indications for skin testing must be weighed carefully against the risk of temporarily aggravating the symptoms by the testing itself. Objective assessment of pulmonary function such as Peak Expiratory Flow Rate (PEFR) before allergen administration and prior to discharge may be useful in unstable asthmatics to reduce the chances of exacerbation of the patient’s asthma. Patients should be instructed to describe any active allergic symptoms as described above prior to skin testing and encouraged to report any late reactions from this testing. Also, see ADVERSE REACTIONS and WARNINGS sections.
  2. Store allergenic extracts between 2o - 8o C at all times, even during use.
  3. Care must be taken to avoid drawing blood.
    1. For percutaneous testing, if blood is observed, immediately wipe the allergen from the site.
    2. For intradermal skin testing, pull gently on the syringe plunger and note if any blood enters the syringe. If blood is obtained, reposition the needle and repeat before injecting (see DOSAGE AND ADMINISTRATION).

  4. Allergenic extracts become less potent with age. Allergenic extracts containing glycerin 50% v/v are relatively stable. Non-glycerinated aqueous extracts, particularly dilute forms as used for intradermal skin testing, have been shown to be extremely unstable. Until such time as stability studies are complete with dilute allergens, new intradermal strength materials should be prepared every few weeks.
  5. Use standard aseptic precautions if making dilutions from stock concentrates to intradermal strength.
  6. For intradermal testing: Extracts in glycerin 50% v/v must be diluted with a non-glycerinated diluent and must be diluted at least 25-fold to less than 2% glycerin by volume, as glycerin above this level can cause false positive intradermal skin test results.

PREGNANCY - CATEGORY C:

Animal reproduction studies have not been conducted with allergenic extracts. It is also not known whether allergenic extracts can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity.

Controlled studies of hyposensitization with moderate to high doses of allergenic extracts during conception and all trimesters of pregnancy have failed to demonstrate any risk to the fetus or to the mother4. However, on the basis of histamine's known ability to contract the uterine muscle, the release of significant amounts of histamine from allergen exposure to skin test overdose should be avoided on theoretical grounds. Therefore, allergenic extracts should be used cautiously in a pregnant woman and only if clearly needed.

Pediatric Use:

Allergenic extracts for diagnostic use have been given safely in infants and young children. Infants have lower skin test reactivity to histamine, as well as common allergens. Skin test reactivity gradually increases to age 6 and plateaus to age 60. Therefore, small skin test reactions should be anticipated in children under age 6.

Geriatric Use:

Skin test reactivity gradually decreases after age 60. Therefore, smaller skin test reactions should be anticipated in adults over age 60.

Nursing Mothers:

It is not known if allergens administered subcutaneously appear in human milk. Because many drugs are excreted in human milk, caution should be exercised when allergenic extracts are administered to a nursing woman.

Carcinogenesis, mutagenesis, impairment of fertility:

Studies in animals have not been performed.

Drug Interactions:

Drugs can interfere with the performance of skin tests5.

Antihistamines: Response to mediator (histamine) released by allergens is suppressed by antihistamines. The length of suppression varies and is dependent on individual patient, type of antihistamine and length of time the patient has been on antihistamines. The duration of this suppression may be as little as 24 hours (chlorpheniramine), and can be as long as 40 days (astemizole).

      Tricyclic Antidepressants: These exert a potent and sustained decrease of skin reactivity to histamine which may last for a few weeks.

      Beta2 Agonists: Oral terbutaline and parenteral ephedrine, in general, have been shown to decrease allergen induced wheal.

      Dopamine: Intravenous infusion of dopamine may inhibit skin test responses.

      Beta Blocking Agents: Propanolol can significantly increase skin test reactivity.

      Other Drugs: Short acting steroids, inhaled beta2 agonists, theophylline and cromolyn do not seem to affect skin test response.

ADVERSE REACTIONS

Fatalities from skin testing in the United States have been extensively reviewed by Lockey.2 Six fatalities were associated with intradermal testing without previous percutaneous testing and one was associated with a combination of percutaneous (scratch) and intradermal skin testing. With careful attention to dosage and administration, fatal reactions occur infrequently, but it must be remembered that allergenic extracts are highly potent to sensitive individuals and overdosage could result in anaphylactic symptoms. Therefore it is imperative that physicians administering allergenic extracts for skin testing understand, and be prepared for the treatment of severe reactions.

Local: Immediate wheal and erythema reactions are to be expected; but if very large, may be the first manifestation of a systemic reaction. In such cases, immediately wipe the test site(s) with sterile gauze or cotton to remove excess allergen.

Systemic Reactions: Systemic reactions are characterized by one or more of the following symptoms: sneezing, mild to severe generalized urticaria, itching (other than at the skin test site), extensive or generalized edema, wheezing, asthma, dyspnea, cyanosis, hypotension, syncope, and upper airway obstruction. Symptoms may progress to shock and death. Patients should always be observed for at least 20 - 30 minutes after testing.

Volume expanders and vasopressor agents may be required to reverse hypotension. Inhalational bronchodilators and parenteral aminophylline may be required to reverse bronchospasm. Severe airway obstruction unresponsive to bronchodilator may require tracheal intubation and use of oxygen. In the event of a marked systemic reaction, application of a tourniquet above the injection site and the administration of 0.02 mL to 1.0 mL of epinephrine injection (1:1,000) is recommended. Maximum recommended dose for children between 2 and 12 years of age is 0.3 mL. The tourniquet should not be left in place without loosening for 90 seconds every 15 minutes.

Adverse events should be reported via MedWatch (1-800-FDA-1088). Adverse experience Reporting, HFM-210 Center for Biologics Evaluation & Research, Food and Drug Administration, 1401 Rockville Pike, Rockville, MD 20852-1448.

OVERDOSAGE

Signs and symptoms of overdose are typically large local and systemic reactions. For management of overdose reactions, refer to the ADVERSE REACTIONS section above.

DOSAGE AND ADMINISTRATION

Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.

Skin test techniques for immediate (Type I) hypersensitivity testing fall into two major categories: percutaneous, and intracutaneous.

Percutaneous techniques: For percutaneous testing, in general, skin is scratched, punctured or pricked just before the allergen is applied or through a drop of test allergen. There are several devices available for this technique. Refer to the manufacturer or distributor's circular for specific directions for their use.

In General:

  1. It is recommended that the test areas should be placed no closer than 4 - 5 cm apart to avoid interference of reactions when several tests are applied.
  2. Skin test areas should be cleansed with alcohol and air dried.
  3. Preferably, the allergen should be placed on the volar surface of the forearm, upper arm, or the patient's back. The patient should be placed in a comfortable position prior to testing.
  4. For scratch testing, a sharp, clean, sterile instrument is used to abrade the skin, but not to draw blood. Each scratch should be about 2 - 4 mm in length. A small drop of extract is placed on the surface of the skin.
  5. Prick testing: For prick testing, a sharp, sterile instrument is used to puncture the skin slightly, applying it at a 15 - 20o angle to the skin. The instrument is gently raised, "tenting” the skin until it pops out, generally pricking through the drop of allergen. Do not draw blood.
  6. For puncture testing, a sharp, clean, sterile instrument must be used. Puncture the skin, through the drop of allergen, perpendicular to the skin. Do not draw blood.

For all of the above techniques, a separate instrument must be used for each patient; if the instrument is to be used to pass through the allergen, to avoid cross-contamination, a separate instrument is to be used for each allergen. The test should be read in 15 minutes, measuring both wheal size and erythema.

Intracutaneous (intradermal) testing: General: Intradermal testing is more sensitive than percutaneous testing and its specificity is dependent on dose. Intradermal testing is not intended as an initial screen unless used in highly dilute solutions. Intradermal testing is usually reserved for allergens that have demonstrated either negative or equivocal percutaneous skin test response in the face of positive or unclear history.

Intradermal testing of one allergen in several serial dilutions (beginning with the weakest to the more concentrated dilutions) may also be useful in assessing degree of patient sensitivity for the establishment of a safe starting dose for immunotherapy.

Bulk extracts must be diluted for intradermal testing. Use of Sterile Diluent for Allergenic Extracts or Sterile Diluent for Allergenic Extracts Normal Saline with HSA (albumin saline) is recommended. Dilutions should be made with sterile disposable syringes using aseptic technique. Commonly, 10 fold dilutions are used to achieve a desired concentration for intradermal testing and continuation of immunotherapy. For example, transferring 0.5 mL of a 10,000 PNU/mL extract into 4.5 mL of diluent will yield 5 mL of extract at 1,000 PNU/mL. For weight volume products, a 1:100 w/v dilution may be prepared from a 1:10 w/v by transferring 0.5 mL of the 1:10 w/v to 4.5 mL of diluent. Prepare as many additional serial dilutions as necessary to reach the appropriate concentration. As a general rule intradermal strength should begin at no higher than 1/100 to 1/1000 of the percutaneous strength that resulted in a negative skin test reaction.

  1. It is recommended that the test areas should be spaced no less than 5 cm apart to avoid interference with adjacent allergen or control.
  2. Skin should be cleansed with alcohol and air dried.
  3. A sterile 1 mL or ½ mL syringe with a 26 - 30 gauge needle should be used. A separate sterile syringe should be used for each extract and each patient.
  4. Care should be taken to eliminate air bubbles from the syringe prior to injecting the test dose. It is suggested that not more than 6 - 10 allergens of each different type be used at any one time. Very sensitive patients may show rapid response.
  5. The skin is held tensely, and the needle is inserted almost parallel to the skin, beveled side up far enough to cover the beveled portion. Slowly inject sufficient extract to make a small bleb of approximately 5 mm in diameter (0.01 - 0.02 mL).
  6. Read the test results in 15 minutes.

Selection of the proper strength for intracutaneous testing: A general rule for the prevention of untoward reactions, particularly in extremely sensitive patients, is to screen by percutaneous methods initially, and begin intradermal testing at a strength not more than 1/100 of a negative or equivocal percutaneous reaction.

Controls: In both percutaneous and intracutaneous tests, a negative control test with diluent alone should be performed because some patients exhibit dermographia, and/or other non-specific irritant responses.

As a positive control in the evaluation of allergenic skin testing, histamine 1 mg/mL (histamine base) should be used for percutaneous testing, and histamine 0.1 mg/mL (histamine base) should be used for intradermal testing.

Interpretation of results: Patient's response is graded on the basis of the size of erythema or wheal.6 General guidelines follow for percutaneous testing, different devices and/or techniques influence the size of the reaction, therefore it is important to refer to the device manufacturer's or distributor's instructions when grading reactions.

Percutaneous (prick or scratch) test:

0 No reaction or less than control.
+ Erythema greater than control, smaller than a nickel (21 mm diameter).
++ Erythema greater than a nickel in diameter, no wheal.
+++ Wheal and erythema without pseudopods.
++++ Wheal and erythema with pseudopods.

Intradermal test:

0 No reaction or less than negative control.
+ 3-4 mm wheal with erythema, or erythema alone larger than a nickel (21 mm diamether).
++ 4-8 mm wheal and erythema, without pseudopods.
+++ Over 8 mm wheal and erythema without pseudopods
++++ Wheal and erythema with pseudopods.

HOW SUPPLIED

For scratch and prick testing: 5 mL dropper applicator vials in 50% v/v glycerin. Available individually and in a complete set of the most common allergens. Available in either Protein Nitrogen Units (PNU/mL) or weight to volume (w/v).

For intracutaneous testing: 5 mL sterile vials, aqueous based, individually and in a complete set of the most common allergens. Available in either Protein Nitrogen Units (PNU/mL) or weight to volume (w/v).

HistatrolR Positive skin test control - histamine. 1 mg/mL and 0.1 mg/mL histamine base.

See Product Catalog for specific diagnostic concentrations available.

STORAGE

To maintain stability of allergenic extracts, proper storage conditions are essential. Bulk concentrates and diluted extracts are to be stored at 2o to 8o C even during use. Bulk or diluted extracts are not to be frozen. Do not use after the expiration date shown on the vial label.

REFERENCES

  1. Holgate, S.T., Robinson, C. and Church, M.K., Mediators of immediate hypersensitivity. In Middleton et al: Allergy Principles and Practice, St. Louis, 1988, C.V. Mosby, p 135.
  2. Lockey, R.F., et al, Fatalities from immunotherapy (IT) and skin testing (ST). J. Allergy Clin. Immunol., 1987:79:660.
  3. Reid, M.J. et al.  Survey of fatalities from skin testing and immunotherapy. 1985-1989. J. Allergy Clin Immunol. 1993; 92:6.
  4. DeBuske L. M. et al.  Special problems regarding Allergen Immunotherapy in Immunology and Allergy Clinics of North America. Greenburger, P.A. Ed. February 1992; 145-149.
  5. Bousquet, J. In vivo methods for the study of allergy: skin test, techniques and interpretation. In: Middleton et al.: Allergy Principles and Practice 3rd Ed. St. Louis: DV Mosby, 1988:167.
  6. Freedman, S.O., Asthma and Allergic Rhinitis II. Clinical Aspects, in Freedman and Gold Clinical Immunology 2nd Ed. New York: Harper & Row, 1976:131.

Revision: June 2002

©ALK-Abello, Inc.                                                 112N

Distributed in Canada by:

Western Allergy Services, LTD.

121-6154 Westminister Highway

Richmond, B.C. V7C404


HOUSE DUST 
house dust   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6000
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HOUSE DUST (HOUSE DUST) HOUSE DUST 10000 [PNU]  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6000-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

ALMOND 
almond food   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6100
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALMOND (ALMOND) ALMOND 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6100-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

APPLE 
apple food   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6101
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
APPLE (APPLE) APPLE 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6101-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

APRICOT 
apricot   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6102
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
APRICOT (APRICOT) APRICOT 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6102-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

ASPARAGUS 
asparagus   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6103
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPARAGUS (ASPARAGUS) ASPARAGUS 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6103-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

AVOCADO 
avocado   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6104
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AVOCADO (AVOCADO) AVOCADO 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6104-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

BANANA 
banana   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6105
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BANANA (BANANA) BANANA 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6105-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

BARLEY 
barley food   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6106
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BARLEY (BARLEY) BARLEY 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6106-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

BEAN 
bean, pinto (kidney)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6107
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BEAN (BEAN) BEAN 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6107-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

STRING BEAN 
bean, string green   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6108
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
STRING BEAN (STRING BEAN) STRING BEAN 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6108-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

BEEF 
beef   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6109
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BEEF (BEEF) BEEF 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6109-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

BRAZIL NUT 
brazil nut   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6110
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BRAZIL NUT (BRAZIL NUT) BRAZIL NUT 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6110-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

BROCCOLI 
broccoli   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6112
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BROCCOLI (BROCCOLI) BROCCOLI 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6112-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

BUCKWHEAT 
buckwheat   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6113
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BUCKWHEAT (BUCKWHEAT) BUCKWHEAT 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6113-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CABBAGE 
cabbage   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6114
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CABBAGE (CABBAGE) CABBAGE 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6114-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CANTALOUPE 
cantaloupe   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6115
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CANTALOUPE (CANTALOUPE) CANTALOUPE 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6115-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CARROT 
carrot   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6116
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CARROT (CARROT) CARROT 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6116-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CASEIN 
casein   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6118
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CASEIN (CASEIN) CASEIN 0.01 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6118-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CELERY 
celery   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6120
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CELERY (CELERY) CELERY 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6120-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CHERRY 
cherry   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6121
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CHERRY (CHERRY) CHERRY 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6121-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CHICKEN 
chicken meat   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6122
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CHICKEN (CHICKEN) CHICKEN 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6122-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CINNAMON 
cinnamon   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6123
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CINNAMON (CINNAMON) CINNAMON 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6123-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CLAM 
clam   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6124
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLAM (CLAM) CLAM 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6124-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

COCOA BEAN 
cocoa, whole bean (chocolate)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6125
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COCOA BEAN (COCOA BEAN) COCOA BEAN 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6125-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

COCONUT 
coconut   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6127
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COCONUT (COCONUT) COCONUT 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6127-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CODFISH 
codfish   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6128
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CODFISH (CODFISH) CODFISH 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6128-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

COFFEE BEAN 
coffee   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6129
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COFFEE BEAN (COFFEE BEAN) COFFEE BEAN 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6129-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CRAB 
crab   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6130
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CRAB (CRAB) CRAB 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6130-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CUCUMBER 
cucumber   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6132
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CUCUMBER (CUCUMBER) CUCUMBER 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6132-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

EGG WHITE 
egg, white   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6133
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EGG WHITE (EGG WHITE) EGG WHITE 0.01 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6133-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

EGG 
egg, whole   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6135
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EGG (EGG) EGG 0.01 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6135-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

EGG YOLK 
egg, yolk   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6136
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EGG YOLK (EGG YOLK) EGG YOLK 0.01 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6136-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

FLOUNDER 
flounder   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6137
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FLOUNDER (FLOUNDER) FLOUNDER 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6137-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

GARLIC 
garlic   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6138
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GARLIC (GARLIC) GARLIC 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6138-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

GRAPE 
grape, white seedless   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6139
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GRAPE (GRAPE) GRAPE 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6139-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

GRAPEFRUIT 
grapefruit   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6141
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GRAPEFRUIT (GRAPEFRUIT) GRAPEFRUIT 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6141-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

KARAYA GUM 
gum, karaya (bassora)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6143
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
KARAYA GUM (KARAYA GUM) KARAYA GUM 0.005 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6143-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

HONEYDEW MELON 
honeydew   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6146
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HONEYDEW MELON (HONEYDEW MELON) HONEYDEW MELON 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6146-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

LAMB 
lamb   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6149
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LAMB (LAMB) LAMB 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6149-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

LEMON 
lemon   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6170
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LEMON (LEMON) LEMON 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6170-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

LETTUCE 
lettuce   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6171
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LETTUCE (LETTUCE) LETTUCE 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6171-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

LIMA BEAN 
lima bean   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6173
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LIMA BEAN (LIMA BEAN) LIMA BEAN 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6173-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

LOBSTER 
lobster   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6174
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LOBSTER (LOBSTER) LOBSTER 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6174-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

GOAT MILK 
milk, goat   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6177
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GOAT MILK (GOAT MILK) GOAT MILK 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6177-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

COW MILK 
milk whole cows   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6178
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COW MILK (COW MILK) COW MILK 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6178-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

MUSHROOM 
mushroom (agaricus spp.)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6180
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CULTIVATED MUSHROOM (CULTIVATED MUSHROOM) CULTIVATED MUSHROOM 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6180-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

MUSTARD SEED 
mustard seed   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6181
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUSTARD SEED (MUSTARD SEED) MUSTARD SEED 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6181-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

OAT 
oat grain   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6183
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OAT (OAT) OAT 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6183-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

BLACK OLIVE 
olive (food)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6185
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BLACK OLIVE (BLACK OLIVE) BLACK OLIVE 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6185-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

ONION 
onion   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6186
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ONION (ONION) ONION 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6186-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

ORANGE 
orange food   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6187
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ORANGE (ORANGE) ORANGE 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6187-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

OYSTER 
oyster   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6189
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OYSTER (OYSTER) OYSTER 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6189-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

PEA 
pea, green (english)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6191
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PEA (PEA) PEA 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6191-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

PEACH 
peach   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6192
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PEACH (PEACH) PEACH 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6192-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

PEANUT 
peanut   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6193
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PEANUT (PEANUT) PEANUT 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6193-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

PEAR 
pear   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6195
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PEAR (PEAR) PEAR 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6195-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

PECAN 
pecan (food)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6196
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PECAN (PECAN) PECAN 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6196-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

GREEN BELL PEPPER 
pepper, bell   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6197
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
GREEN BELL PEPPER (GREEN BELL PEPPER) GREEN BELL PEPPER 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6197-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

PEPPER 
pepper, black   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6198
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PEPPER (PEPPER) PEPPER 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6198-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

PINEAPPLE 
pineapple   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6200
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PINEAPPLE (PINEAPPLE) PINEAPPLE 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6200-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

PISTACHIO 
pistachio nut   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6202
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PISTACHIO (PISTACHIO) PISTACHIO 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6202-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

PLUM 
plum   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6203
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PLUM (PLUM) PLUM 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6203-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

PORK 
pork   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6204
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PORK (PORK) PORK 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6204-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

POTATO 
potato, sweet   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6205
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
POTATO (POTATO) POTATO 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6205-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

POTATO 
potato, white   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6206
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
POTATO (POTATO) POTATO 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6206-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

RICE 
rice   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6208
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RICE (RICE) RICE 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6208-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

RYE 
rye (food)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6210
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RYE (RYE) RYE 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6210-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

SALMON 
salmon   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6212
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SALMON (SALMON) SALMON 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6212-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

SESAME SEED 
sesame seed   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6213
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SESAME SEED (SESAME SEED) SESAME SEED 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6213-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

SHRIMP 
shrimp   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6214
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SHRIMP (SHRIMP) SHRIMP 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6214-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

SOYBEAN 
soybean   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6216
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SOYBEAN (SOYBEAN) SOYBEAN 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6216-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

SPINACH 
spinach   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6218
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SPINACH (SPINACH) SPINACH 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6218-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

SQUASH 
squash   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6219
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SQUASH (SQUASH) SQUASH 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6219-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

STRAWBERRY 
strawberry   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6220
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
STRAWBERRY (STRAWBERRY) STRAWBERRY 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6220-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CORN 
sweet corn (food)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6221
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CORN (CORN) CORN 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6221-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

TOMATO 
tomato   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6224
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TOMATO (TOMATO) TOMATO 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6224-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

TUNA 
tuna   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6226
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TUNA (TUNA) TUNA 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6226-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

TURKEY 
turkey meat   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6229
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TURKEY (TURKEY) TURKEY 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6229-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

VANILLA 
vanilla   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6230
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
VANILLA (VANILLA) VANILLA 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6230-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

ENGLISH WALNUT 
walnut, english (food)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6231
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ENGLISH WALNUT (ENGLISH WALNUT) ENGLISH WALNUT 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6231-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

WATERMELON 
watermelon   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6233
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
WATERMELON (WATERMELON) WATERMELON 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6233-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

WHEAT 
wheat, whole (wheat grain)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6234
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
WHEAT (WHEAT) WHEAT 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6234-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

BOS TAURUS SKIN 
cattle epithelium   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6300
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BOS TAURUS SKIN (BOS TAURUS SKIN) BOS TAURUS SKIN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6300-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

COTTON FIBER 
cattle epithelium   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6302
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COTTON FIBER (COTTON FIBER) COTTON FIBER 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6302-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

COTTON SEED 
cottonseed   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6304
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COTTON SEED (COTTON SEED) COTTON SEED 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6304-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CANIS LUPUS FAMILIARIS SKIN 
dog epithelium   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6306
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CANIS LUPUS FAMILIARIS SKIN (CANIS LUPUS FAMILIARIS SKIN) CANIS LUPUS FAMILIARIS SKIN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6306-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CAVIA PORCELLUS SKIN 
guinea pig epithelium   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6309
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CAVIA PORCELLUS SKIN (CAVIA PORCELLUS SKIN) CAVIA PORCELLUS SKIN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6309-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

EQUUS CABALLUS SKIN 
horse epithelium   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6311
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EQUUS CABALLUS SKIN (EQUUS CABALLUS SKIN) EQUUS CABALLUS SKIN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6311-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CEIBA PENTANDRA FIBER 
kapok   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6312
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CEIBA PENTANDRA FIBER (CEIBA PENTANDRA FIBER) CEIBA PENTANDRA FIBER 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6312-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

MUS MUSCULUS SKIN 
mouse epithelium   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6314
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUS MUSCULUS SKIN (MUS MUSCULUS SKIN) MUS MUSCULUS SKIN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6314-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

ORRIS 
orris root   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6317
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ORRIS (ORRIS) ORRIS 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6317-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

PYRETHRUM CINERARIIFOLIUM 
pyrethrum   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6318
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PYRETHRUM CINERARIIFOLIUM (PYRETHRUM CINERARIIFOLIUM) PYRETHRUM CINERARIIFOLIUM 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6318-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

RABBIT 
rabbit epithelium   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6320
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RABBIT (RABBIT) RABBIT 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6320-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

SOLENOPSIS INVICTA 
ant, fire   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6400
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SOLENOPSIS INVICTA (SOLENOPSIS INVICTA) SOLENOPSIS INVICTA 0.01 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6400-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

PERIPLANETA AMERICANA 
cockroach, american   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6403
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PERIPLANETA AMERICANA (PERIPLANETA AMERICANA) PERIPLANETA AMERICANA 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6403-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

BLATELLA GERMANICA 
cockroach, german   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6405
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BLATELLA GERMANICA (BLATELLA GERMANICA) BLATELLA GERMANICA 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6405-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

ACREMONIUM STRICTUM 
acremonium strictum   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6500
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACREMONIUM STRICTUM (ACREMONIUM STRICTUM) ACREMONIUM STRICTUM 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6500-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

ALTERNARIA TENUIS 
alternaria tenuis (a. alternata)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6502
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALTERNARIA ALTERNATA (ALTERNARIA ALTERNATA) ALTERNARIA ALTERNATA 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6502-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

ASPERGILLUS FUMIGATUS 
aspergillus fumigatus   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6504
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS FUMIGATUS (ASPERGILLUS FUMIGATUS) ASPERGILLUS FUMIGATUS 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6504-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

ASPERGILLUS NIGER VAR. NIGER 
aspergillus niger   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6507
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ASPERGILLUS NIGER VAR. NIGER (ASPERGILLUS NIGER VAR. NIGER) ASPERGILLUS NIGER VAR. NIGER 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6507-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

AUREOBASIDIUM PULLULANS VAR. PULLULANS 
pullularia pullulans   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6509
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AUREOBASIDIUM PULLULANS VAR. PULLUTANS (AUREOBASIDIUM PULLULANS VAR. PULLUTANS) AUREOBASIDIUM PULLULANS VAR. PULLUTANS 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6509-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

BOTRYTIS CINEREA 
botrytis cinerea   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6512
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BOTRYTIS CINEREA (BOTRYTIS CINEREA) BOTRYTIS CINEREA 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6512-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CANDIDA ALBICANS 
candida albicans   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6514
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CANDIDA ALBICANS (CANDIDA ALBICANS) CANDIDA ALBICANS 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6514-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CHAETOMIUM GLOBOSUM 
chaetomium globosum   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6516
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CHAETOMIUM GLOBOSUM (CHAETOMIUM GLOBOSUM) CHAETOMIUM GLOBOSUM 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6516-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CLADOSPORIUM CLADOSPORIOIDES 
cladosporium cladosporioides (hormodendrum clad.)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6518
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLADOSPORIUM CLADOSPORIOIDES (CLADOSPORIUM CLADOSPORIOIDES) CLADOSPORIUM CLADOSPORIOIDES 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6518-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CLADOSPORIUM SPHAEROSPERMUM 
cladosporium sphaerospermum (hormodendrum hordei)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6520
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CLADOSPORIUM SPHAEROSPERMUM (CLADOSPORIUM SPHAEROSPERMUM) CLADOSPORIUM SPHAEROSPERMUM 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6520-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

COCHLIOBOLUS SATIVUS 
helminthosporium sorokinianum   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6524
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
COCHLIOBOLUS SATIVUS (COCHLIOBOLUS SATIVUS) COCHLIOBOLUS SATIVUS 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6524-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

EPICOCCUM NIGRUM 
epicoccum nigrum   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6526
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
EPICOCCUM NIGRUM (EPICOCCUM NIGRUM) EPICOCCUM NIGRUM 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6526-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

FUSARIUM OXYSPORUM VASINFECTUM 
fusarium spp.   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6529
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FUSARIUM OXYSPORUM VASINFECTUM (FUSARIUM OXYSPORUM VASINFECTUM) FUSARIUM OXYSPORUM VASINFECTUM 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6529-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

HELMINTHOSPORIUM SOLANI 
helminthosporium solani (spondylocladium)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6533
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HELMINTHOSPORIUM SOLANI (HELMINTHOSPORIUM SOLANI) HELMINTHOSPORIUM SOLANI 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6533-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

MUCOR PLUMBEUS 
mucor spp.   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6536
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MUCOR PLUMBEUS (MUCOR PLUMBEUS) MUCOR PLUMBEUS 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6536-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

NEUROSPORA INTERMEDIA 
neurospora spp.   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6538
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
NEUROSPORA INTERMEDIA (NEUROSPORA INTERMEDIA) NEUROSPORA INTERMEDIA 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6538-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

KHUSKIA ORYZAE 
nigrospora spp.   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6540
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
KHUSKIA ORYZAE (KHUSKIA ORYZAE) KHUSKIA ORYZAE 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6540-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

PHOMA EXIGUA VAR. EXIGUA 
phoma herbarum   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6543
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PHOMA EXIGUA VAR. EXIGUA (PHOMA EXIGUA VAR. EXIGUA) PHOMA EXIGUA VAR. EXIGUA 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6543-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

RHIZOPUS ARRHIZUS VAR. ARRHIZUS 
rhizopus spp.   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6545
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHIZOPUS ARRHIZUS VAR. ARRHIZUS (RHIZOPUS ARRHIZUS VAR. ARRHIZUS) RHIZOPUS ARRHIZUS VAR. ARRHIZUS 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6545-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

RHODOTORULA RUBRA 
rhodotorula rubra   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6548
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RHODOTORULA RUBRA (RHODOTORULA RUBRA) RHODOTORULA RUBRA 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6548-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

USTILAGO MAYDIS 
smut, corn   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6550
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
USTILAGO MAYDIS (USTILAGO MAYDIS) USTILAGO MAYDIS 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6550-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

USTILAGO TRITICI 
smut, wheat   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6552
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
USTILAGO TRITICI (USTILAGO TRITICI) USTILAGO TRITICI 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6552-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

STEMPHYLIUM SOLANI 
stemphylium spp.   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6553
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
STEMPHYLIUM SOLANI (STEMPHYLIUM SOLANI) STEMPHYLIUM SOLANI 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6553-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

TRICHOPHYTON MENTAGROPHYTES 
trichophyton mentagrophytes   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6556
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICHOPHYTON MENTAGROPHYTES (TRICHOPHYTON MENTAGROPHYTES) TRICHOPHYTON MENTAGROPHYTES 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6556-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 
yeast (saccharomyces cerevisiae)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6558
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM) PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM 0.10 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6558-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

ACACIA 
acacia   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6600
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACACIA (ACACIA) ACACIA 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6600-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

ALNUS INCANA SSP. RUGOSA POLLEN 
alder, white   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6601
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALNUS INCANA SUBSP. RUGOSA POLLEN (ALNUS INCANA SUBSP. RUGOSA POLLEN) ALNUS INCANA SUBSP. RUGOSA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6601-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

MEDICAGO SATIVA POLLEN 
alfalfa   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6602
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MEDICAGO SATIVA POLLEN (MEDICAGO SATIVA POLLEN) MEDICAGO SATIVA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6602-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

FRAXINUS AMERICANA POLLEN 
ash, white   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6603
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FRAXINUS AMERICANA POLLEN (FRAXINUS AMERICANA POLLEN) FRAXINUS AMERICANA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6603-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

PASPALUM NOTATUM POLLEN 
bahia grass   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6605
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PASPALUM NOTATUM POLLEN (PASPALUM NOTATUM POLLEN) PASPALUM NOTATUM POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6605-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

MORELLA CERIFERA POLLEN 
bayberry (wax myrtle)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6606
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MORELLA CERIFERA POLLEN (MORELLA CERIFERA POLLEN) MORELLA CERIFERA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6606-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

FAGUS GRANDIFOLIA POLLEN 
beech   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6607
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
FAGUS GRANDIFOLIA POLLEN (FAGUS GRANDIFOLIA POLLEN) FAGUS GRANDIFOLIA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6607-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

BETULA LENTA POLLEN 
birch, black   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6608
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BETULA LENTA POLLEN (BETULA LENTA POLLEN) BETULA LENTA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6608-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

BETULA NIGRA POLLEN 
birch, river (red)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6609
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BETULA NIGRA POLLEN (BETULA NIGRA POLLEN) BETULA NIGRA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6609-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

BETULA LENTA POLLEN 
birch, white   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6610
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
BETULA LENTA POLLEN (BETULA LENTA POLLEN) BETULA LENTA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6610-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

ACER NEGUNDO POLLEN 
box elder (ash leaf maple)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6612
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACER NEGUNDO POLLEN (ACER NEGUNDO POLLEN) ACER NEGUNDO POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6612-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

AMARANTHUS PALMERI POLLEN 
carelessweed   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6613
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AMARANTHUS PALMERI POLLEN (AMARANTHUS PALMERI POLLEN) AMARANTHUS PALMERI POLLEN 0.025 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6613-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

JUNIPERUS ASHEI POLLEN 
cedar, mountain   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6614
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
JUNIPERUS ASHEI POLLEN (JUNIPERUS ASHEI POLLEN) JUNIPERUS ASHEI POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6614-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

JUNIPERUS VIRGINIANA POLLEN 
cedar, red   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6615
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
JUNIPERUS VIRGINIANA POLLEN (JUNIPERUS VIRGINIANA POLLEN) JUNIPERUS VIRGINIANA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6615-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN 
cocklebur   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6616
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN (XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN) XANTHIUM STRUMARIUM VAR. CANADENSE POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6616-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

POPULUS DELTOIDES POLLEN 
cottonwood, eastern (common)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6618
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
POPULUS DELTOIDES POLLEN (POPULUS DELTOIDES POLLEN) POPULUS DELTOIDES POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6618-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CUPRESSUS ARIZONICA POLLEN 
cypress, arizona   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6619
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CUPRESSUS ARIZONICA POLLEN (CUPRESSUS ARIZONICA POLLEN) CUPRESSUS ARIZONICA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6619-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

TAXODIUM DISTICHUM POLLEN 
cypress, bald   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6620
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TAXODIUM DISTICHUM POLLEN (TAXODIUM DISTICHUM POLLEN) TAXODIUM DISTICHUM POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6620-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

RUMEX ACETOSELLA POLLEN 
dock, sour (sheep sorrel)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6621
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RUMEX ACETOSELLA POLLEN (RUMEX ACETOSELLA POLLEN) RUMEX ACETOSELLA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6621-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

RUMEX CRISPUS POLLEN 
dock, yellow   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6622
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
RUMEX CRISPUS POLLEN (RUMEX CRISPUS POLLEN) RUMEX CRISPUS POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6622-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

ULMUS AMERICANA POLLEN 
elm, american   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6623
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ULMUS AMERICANA POLLEN (ULMUS AMERICANA POLLEN) ULMUS AMERICANA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6623-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

SOLIDAGO CANADENSIS POLLEN 
goldenrod   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6625
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SOLIDAGO CANADENSIS POLLEN (SOLIDAGO CANADENSIS POLLEN) SOLIDAGO CANADENSIS POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6625-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CELTIS OCCIDENTALIS POLLEN 
hackberry   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6626
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CELTIS OCCIDENTALIS POLLEN (CELTIS OCCIDENTALIS POLLEN) CELTIS OCCIDENTALIS POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6626-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CARYA OVATA POLLEN 
hickory, shagbark   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6627
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CARYA OVATA POLLEN (CARYA OVATA POLLEN) CARYA OVATA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6627-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

SORGHUM HALEPENSE POLLEN 
johnson grass   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6629
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SORGHUM HALEPENSE POLLEN (SORGHUM HALEPENSE POLLEN) SORGHUM HALEPENSE POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6629-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

JUNIPERUS CALIFORNICA POLLEN 
juniper, western   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6630
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
JUNIPERUS CALIFORNICA POLLEN (JUNIPERUS CALIFORNICA POLLEN) JUNIPERUS CALIFORNICA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6630-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

KOCHIA SCOPARIA POLLEN 
kochia (firebush)   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6631
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
KOCHIA SCOPARIA POLLEN (KOCHIA SCOPARIA POLLEN) KOCHIA SCOPARIA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6631-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

CHENOPODIUM ALBUM POLLEN 
lambs quarters   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6632
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CHENOPODIUM ALBUM POLLEN (CHENOPODIUM ALBUM POLLEN) CHENOPODIUM ALBUM POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6632-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

ACER RUBRUM POLLEN 
maple, red   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6634
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACER RUBRUM POLLEN (ACER RUBRUM POLLEN) ACER RUBRUM POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6634-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

ACER SACCHARUM POLLEN 
maple, sugar   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6635
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACER SACCHARUM POLLEN (ACER SACCHARUM POLLEN) ACER SACCHARUM POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6635-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

IVA XANTHIFOLIA POLLEN 
marshelder, burweed   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6636
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
IVA XANTHIFOLIA POLLEN (IVA XANTHIFOLIA POLLEN) IVA XANTHIFOLIA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6636-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

IVA ANNUA VAR. ANNUA POLLEN 
marshelder, rough   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6637
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
IVA ANNUA VAR. ANNUA POLLEN (IVA ANNUA VAR. ANNUA POLLEN) IVA ANNUA VAR. ANNUA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6637-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

PROSOPIS JULIFLORA POLLEN 
mesquite   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6638
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PROSOPIS JULIFLORA POLLEN (PROSOPIS JULIFLORA POLLEN) PROSOPIS JULIFLORA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6638-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

ARTEMISIA VULGARIS POLLEN 
mugwort, common   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6639
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ARTEMISIA VULGARIS POLLEN (ARTEMISIA VULGARIS POLLEN) ARTEMISIA VULGARIS POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6639-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

MORUS RUBRA POLLEN 
mulberry, red   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6640
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MORUS RUBRA POLLEN (MORUS RUBRA POLLEN) MORUS RUBRA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6640-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

MORUS ALBA POLLEN 
mulberry, white   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6641
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MORUS ALBA POLLEN (MORUS ALBA POLLEN) MORUS ALBA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6641-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

QUERCUS RUBRA POLLEN 
oak, red   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6642
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
QUERCUS RUBRA POLLEN (QUERCUS RUBRA POLLEN) QUERCUS RUBRA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6642-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

QUERCUS VIRGINIANA POLLEN 
oak, virginia live   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6643
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
QUERCUS VIRGINIANA POLLEN (QUERCUS VIRGINIANA POLLEN) QUERCUS VIRGINIANA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 0268-6643-06 5 mL In 1 VIAL, MULTI-DOSE None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
BLA BLA103753 01/01/1965

QUERCUS ALBA POLLEN 
oak, white   injection, solution
Product Information
Product Type NON-STANDARDIZED ALLERGENIC NDC Product Code (Source) 0268-6644
Route of Administration PERCUTANEOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
QUERCUS ALBA POLLEN (QUERCUS ALBA POLLEN) QUERCUS ALBA POLLEN 0.05 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
GLYCERIN 0.5 mL  in 1 mL
PHENOL 0.004 mL  in 1 mL
SODIUM CHLORIDE 0.009 g  in 1 mL
SODIUM BICARBONATE 0.00275 g  in 1 mL
HYDROCHLORIC ACID  
SODIUM HYDROXIDE  
Product Characteristics
Color      Score     
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Packaging
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