Label: ADDITIVE FORMULA 3- dextrose monohydrate, trisodium citrate dihydrate, sodium chloride, sodium phosphate, monobasic, monohydrate, citric acid monohydrate, and adenine solution

  • NDC Code(s): 14537-824-10, 14537-826-20, 14537-828-35
  • Packager: Terumo BCT, Ltd
  • Category: HUMAN PRESCRIPTION DRUG LABEL

Drug Label Information

Updated April 26, 2019

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  • HIGHLIGHTS OF PRESCRIBING INFORMATION
    These highlights do not include all the information needed to use ADDITIVE SOLUTION FORMULA 3 (AS-3) safely and effectively. See full prescribing information for ADDITIVE SOLUTION FORMULA 3 (AS-3).

    ADDITIVE SOLUTION FORMULA 3 (AS-3)

    Sterile Fluid
    Polyolefin Bag

    Initial U.S. Approval: 2002

    INDICATIONS AND USAGE

    Use only with Trima Accel red blood cell (RBC) apheresis collections. (1)

    DOSAGE AND ADMINISTRATION

    • AS-3 is added to tubing sets after apheresis collections, after the donor has been disconnected. (2)
    • AS-3 may only be used with the Trima Accel apheresis device. For instructions on the use of the solution see the device operator's manual. (2.1)
    • Follow the directions for connecting the AS-3 bag to the tubing set of a blood collection system. (2.2)

    DOSAGE FORMS AND STRENGTHS

    • 100 mL, 200 mL, or 350 mL sterile fluid in a Polyolefin bag. (3)

    CONTRAINDICATIONS

    • DO NOT INFUSE AS-3 DIRECTLY TO THE DONOR. (4)

    WARNINGS AND PRECAUTIONS

    • Verify that the AS-3 bag has been securely attached to the system tubing set. Use aseptic technique throughout all procedures to ensure product quality. (5)
    • Do not reuse. Discard unused or partially used solution bags.

    ADVERSE REACTIONS

    Citrate reactions or toxicity may occur with the infusion of blood containing citrate. The recipient of the blood containing citrate should be monitored for the signs and symptoms of citrate toxicity. (6)


    To report SUSPECTED ADVERSE REACTIONS, contact Terumo BCT, Inc. at 1-877-339-4228 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

    Revised: 7/2018

  • Table of Contents

    FULL PRESCRIBING INFORMATION: CONTENTS*

    1 INDICATIONS AND USAGE

    2 DOSAGE AND ADMINISTRATION

    2.1 General Dosing Information

    2.2 Administration

    3 DOSAGE FORMS AND STRENGTHS

    4 CONTRAINDICATIONS

    5 WARNINGS AND PRECAUTIONS

    6 ADVERSE REACTIONS

    8 USE IN SPECIFIC POPULATIONS

    11 DESCRIPTION

    12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    14 CLINICAL STUDIES

    16 HOW SUPPLIED/STORAGE AND HANDLING

    *
    Sections or subsections omitted from the full prescribing information are not listed.
  • 1 INDICATIONS AND USAGE

    Use only with Trima Accel red blood cell (RBC) apheresis collections. [See Dosage and Administration (2).]

  • 2 DOSAGE AND ADMINISTRATION

    2.1 General Dosing Information

    ADDITIVE SOLUTION FORMULA 3 (AS-3) is connected to the tubing set used for an apheresis RBC collection procedure after the collection has been completed.

    • For automated RBC procedures, the recommended dose is determined by the apheresis device and metered into the tubing set by the apheresis device.
    • To add the product manually, refer to the apheresis system operator's manual to determine the recommended dose.

    For instructions on the use of the solution with the apheresis device and tubing set, see the device operator's manual.

    2.2 Administration

    Directions for connecting the ADDITIVE SOLUTION FORMULA 3 (AS-3) bag to the apheresis device.

    Automated RBC additive solution procedures:

    Connect ADDITIVE SOLUTION FORMULA 3 (AS-3) after the collection is over and the donor is disconnected. For automated addition of the product, the system will prompt you to connect the bag.

    1. Remove the overwrap by pulling down at notch, and remove the AS-3 bag.
    2. Before use, perform the following checks:
      • Ensure that the solution is the ADDITIVE SOLUTION FORMULA 3 (AS-3) and is within the expiration date.
      • Inspect the bag in good light. Do not use if the container is damaged, leaking or if there is any visible sign of deterioration. Check for leaks by gently squeezing the bag. If leaks are found, discard the bag.
      • Inspect the solution in good light. Use only if solution is clear and free of particulate matter. Bags showing cloudiness, haze, or particulate matter should not be used.
      • Protect from sharp objects.
    3. Remove the protective cap from the port on the bag.
    4. Connect the bag to the apheresis device tubing set using aseptic technique and hang the solution.
    5. Break the frangible connector. When you break frangible connectors, bend them in both directions to ensure that you break them completely. Failure to do so may result in restricted flow.
    6. Proceed according to the apheresis device operator's manual.

    Manual RBC additive solution procedures:

    Connect ADDITIVE SOLUTION FORMULA 3 (AS-3) after the collection is over and the donor is disconnected.

    1. Seal the RBC product lines as close to the cassette as possible.
    2. Remove the overwrap by pulling down at notch, and remove the ADDITIVE SOLUTION FORMULA 3 bag.
    3. Before use, perform the following checks:
      • Ensure that the solution is the ADDITIVE SOLUTION FORMULA 3 (AS-3) and is within the expiration date.
      • Inspect the bag in good light. Do not use if the container is damaged, leaking or if there is any visible sign of deterioration. Check for leaks by gently squeezing the bag. If leaks are found, discard the bag.
      • Inspect the solution in good light. Use only if solution is clear and free of particulate matter. Bags showing cloudiness, haze, or particulate matter should not be used.
      • Protect from sharp objects.
    4. Remove the protective cap from the port on the bag.
    5. Connect the bag to the apheresis device tubing set using aseptic technique and hang the solution.
    6. Break the frangible connector. When you break frangible connectors, bend them in both directions to ensure that you break them completely. Failure to do so may result in restricted flow.
    7. Proceed according to the apheresis device operator's manual.
  • 3 DOSAGE FORMS AND STRENGTHS

    100 mL, 200 mL and 350 mL ADDITIVE SOLUTION FORMULA 3 (AS-3) products are sterile solutions in a Polyolefin bag. Each 100 mL contains: Dextrose Monohydrate USP 1.10 g; Trisodium Citrate Dihydrate USP 0.59 g; Sodium Chloride USP 0.41 g; Monobasic Sodium Phosphate Monohydrate USP 0.28 g; Citric Acid Monohydrate USP 0.042 g; Adenine USP 0.03 g; and Water for Injection USP.

  • 4 CONTRAINDICATIONS

    DO NOT INFUSE ADDITIVE SOLUTION FORMULA 3 (AS-3) DIRECTLY TO THE DONOR.

  • 5 WARNINGS AND PRECAUTIONS

    • Verify that the AS-3 bag has been securely attached to the system tubing set. Use aseptic technique throughout all procedures to ensure product quality.
    • Do not reuse. Discard unused or partially used solution bags.
  • 6 ADVERSE REACTIONS

    Citrate reactions or toxicity may occur with the infusion of blood products to patients. The recipient of the blood containing citrate should be monitored for the signs and symptoms of citrate toxicity. The signs and symptoms of citrate toxicity begin with paresthesia, a "tingling" sensation around the mouth or in the extremities, followed by severe reactions that are characterized by hypotension and possible cardiac arrhythmia. Citrate toxicity may occur more frequently in patients who are hypothermic, have impaired liver or renal function, or have low calcium levels because of an underlying disease.

  • 8 USE IN SPECIFIC POPULATIONS

    ADDITIVE SOLUTION FORMULA 3 (AS-3) has not been studied in controlled clinical trials with specific populations.

  • 11 DESCRIPTION

    ADDITIVE SOLUTION FORMULA 3 (AS-3) is designed to be added to packed RBC collected in apheresis procedures, and acts to preserve and extend the shelf life of packed RBC products for later transfusion to patients. The solution is intended to be metered by an apheresis device during apheresis procedures or added manually after a collection.

    The solution is sterile and non-pyrogenic, and it contains no bacteriostatic or antimicrobial agents.

    The formulas of the active ingredients are provided in Table 1.

    Table 1: Active Ingredients
    IngredientsMolecular FormulaMolecular Weight
    Dextrose Monohydrate USPC6H12O6 ∙ H2O198.17
    Trisodium Citrate Dihydrate USPC6H9Na3O9294.10
    Sodium Chloride USPNaCl58.44
    Monobasic Sodium Phosphate Monohydrate USPNaH2PO4 ∙ H2O137.99
    Citric Acid Monohydrate USPC6H807 ∙ H2O210.14
    Adenine USPC5H5N5135.13
    Water for Injection USPH2O18.00

    Each 100 mL of ADDITIVE SOLUTION FORMULA 3 (AS-3) contains: Dextrose Monohydrate USP 1.10 g; Trisodium Citrate Dihydrate USP 0.59 g; Sodium Chloride USP 0.41 g; Monobasic Sodium Phosphate Monohydrate USP 0.28 g; Citric Acid Monohydrate USP 0.042 g; Adenine USP 0.03 g; and Water for Injection USP.

    ADDITIVE SOLUTION FORMULA 3 is available in three volumes: 100 mL, 200 mL and 350 mL.

    The 100 mL bags are individually wrapped with a clear plastic film. Six individually wrapped bags are then vacuum-sealed in a foil pouch, which serves as a vapor barrier to prevent water loss during storage. After you remove the individual solution bags from the foil pouch, you can either leave them in the clear plastic film or remove and discard it. Once the foil pouch has been opened, use all six of the solution bags within 2 weeks.

    The 200 mL and 350 mL bags are individually wrapped with a clear plastic film. These larger volumes do not require the additional vapor barrier. Once the clear plastic film has been removed, use the solution within 2 weeks.

    The Polyolefin bag is not made with natural rubber latex.

    The bag is made from a multilayered film. It contains materials that have been tested to demonstrate the suitability of the container for storing pharmaceutical solutions. The bag is nontoxic and biologically inert. The bag-solution unit is a closed system and is not dependent upon entry of external air during administration.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    ADDITIVE SOLUTION FORMULA 3 acts to preserve and extend the shelf life of packed RBC products for later transfusion to patients. The following ingredients are key components of the solution:

    • Adenine to support adenosine triphosphate (ATP) levels
    • Citrate for membrane protection, anticoagulation and pH regulation
    • Sodium (Sodium Chloride and Sodium Citrate) and dextrose for isotonicity
    • Dextrose for RBC nutrition

    This solution has no pharmacological effect.

  • 14 CLINICAL STUDIES

    The in vivo and in vitro quality of RBCs stored for 42 days in ADDITIVE SOLUTION FORMULA 3 (AS-3) storage solution has been assessed in three clinical studies.

    In Vivo Recovery of Autologous Radiolabeled RBC

    A single-arm, multicenter, in vivo study was conducted to assess the recovery of radiolabeled RBCs 24 hours post infusion. Acceptability of in vivo recovery was determined using established FDA-CBER acceptance criteria. Double collection RBCs (dRBC) were collected using the Trima Accel system and stored in ADDITIVE SOLUTION FORMULA 3 (AS-3) solution for 42 days, then radiolabeled with 51Chromium, and transfused back to the original subject. Table 2 summarizes the in vivo recovery data. Of the 27 units transfused, 26 had > 75% RBC recovery.

    Table 2: In vivo Radiolabeled RBC Recovery
    Outcome MeasureStudy Site (N)Average (SD)Min, Max
    Abbreviations: Max= Maximum, Min= Minimum, N= Number of Units Transfused, RBC= Red Blood Cell, SD= Standard Deviation
    Overall Day 42 infused, 24-hour RBC Radiolabel Recovery (%)Site 1 (12)79.3 (5.6)67.5, 86.5
    Site 2 (15)87.1 (5.5)79.0, 98.1

    FDA-CBER Criteria for Acceptable Recovery: Radiolabeled RBC recoveries should average at least 75%, with a standard deviation of at most 9%. In addition, the 95% one-sided lower confidence limit for the population proportion of successes should be > 70%, with success being defined as an individual red blood cell in vivo recovery of at least 75%. No more than 3 out of 24 data points may have less than 75% radiolabeled red cell recovery at 24 hours post infusion.

    The primary outcome was met for RBCs collected on the Trima Accel system and stored in ADDITIVE SOLUTION FORMULA 3 (AS-3) storage solution.

    In Vitro RBC Quality Studies

    The in vitro quality of RBCs collected in single RBC collection (sRBC) and dRBC procedures using the Trima Accel system was assessed after 42 days of storage in ADDITIVE SOLUTION FORMULA 3 (AS-3) solution in a multicenter, paired study. In vitro quality was determined using established FDA-CBER acceptance criteria. The quality of RBCs stored in ADDITIVE SOLUTION FORMULA 3 (AS-3) solution (test) was compared to RBCs stored in plasma (control). Table summarizes the in vitro RBC quality data for collection on the Trima Accel system and storage in ADDITIVE SOLUTION FORMULA 3 (AS-3) solution.

    Table 3: In Vitro Quality Measures for RBCs Collected using the Trima Accel System and Stored in ADDITIVE SOLUTION FORMULA 3 (AS-3)
    Outcome MeasureSite (N)Average (SD)Min, Max
    Abbreviations: HCT = hematocrit, HgB = hemoglobin, Max = Maximum, Min = Minimum, N = Number of Units, RBC = Red Blood Cell, SD = Standard Deviation
    *
    Percent hemolysis was calculated from plasma free hemoglobin using the equation:
    %Hemolysis = (100 – RBC Product HCT)* Plasma Hgb / (RBC Product Hgb).
    †
    The difference in pH between Test and Control on Day 42 was calculated as:
    ΔpH = │pHTest – pHControl│ ≤ 0.5
    where the difference was expected to be less than or equal to 0.5 pH units.
    ‡
    ATP retention was determined for test and control units across all sites and calculated as ATP Level on Day 42 / ATP Level on Day 0.
    §
    Normalized potassium was calculated by determining the total number of millimoles of potassium leaked from the RBCs into the supernatant volume and dividing this by the total hemoglobin in the stored product.
    Normalized Leaked Potassium = Volume*(1-Hct/100)*(d42[K+] – d0[K+]) / Total Hemoglobin
    Day 42 Hemolysis for Single RBC Collection* (%)Site 1 (32)0.16 (0.06)0.06, 0.33
    Site 2 (18)0.34 (0.18)0.12, 0.70
    Site 3 (18)0.26 (0.11)0.09, 0.47
    Day 42 Hemolysis for Double RBC Collection* (%)Site 1 (25)0.15 (0.05)0.06, 0.29
    Site 2 (24)0.39 (0.19)0.16, 0.95
    Site 3 (21)0.26 (0.12)0.13, 0.61
    Change in pH from Day 0 to Day 42 for Single RBC Collection†Site 1 (31)0.03 (0.02)0.00, 0.08
    Site 2 (18)0.03 (0.03)0.00, 0.11
    Site 3 (16)0.02 (0.02)0.00, 0.07
    Change in pH from Day 0 to Day 42 for Double RBC Collection†Site 1 (23)0.02 (0.02)0.00, 0.05
    Site 2 (23)0.02 (0.03)0.00, 0.15
    Site 3 (19)0.02 (0.02)0.00, 0.08
    Ratio of ATP Retention for Single Collection RBC Units (test/control)‡All sites (65)1.02 (0.18)0.46, 1.47
    Ratio of ATP Retention for Double Collection RBC Units (test/control)‡All sites (65)1.07 (0.19)0.55, 1.51
    Ratio of the Normalized Leaked Potassium for Single Collection RBC Units (test/control)§All sites (65)0.98 (0.07)0.76, 1.13
    Ratio of the Normalized Leaked Potassium for Double Collection RBC Units (test/control)§All Sites (64)1.00 (0.08)0.85, 1.24

    FDA-CBER Criteria for Acceptable Day 42 Hemolysis: Zero failures (hemolysis ≥ 1% after 42-day storage) out of 60 test units that were not excluded from analysis by the Extreme Studentized Deviate test with α=0.05, which satisfies the binomial distribution testing requirement that, with 95% probability and a one-sided 95% lower confidence limit, the post-storage hemolysis was less than 1% per unit.

    There were 0/68 sRBC test units and 0/70 dRBC test units with Day 42 hemolysis ≥ 1%. No donors were excluded as hemolysis was < 1% for all test units. Therefore, the primary objective was met for RBCs stored in ADDITIVE SOLUTION FORMULA 3 (AS-3).

    The in vitro quality of sRBC and dRBC units collected using the Trima Accel system was assessed after 42 days of storage in AS-3 solution in a multicenter study. The quality of RBCs was compared between sRBC and dRBC units, and between units A and B of the dRBC collection. Table summarizes the in vitro RBC quality data for collection using the Trima Accel system and storage in ADDITIVE SOLUTION FORMULA 3 (AS-3).

    Table 4: In Vitro Quality Measures for RBCs Collected using the Trima Accel System and Stored in ADDITIVE SOLUTION FORMULA 3 (AS-3)
    Outcome Measure*SiteRBC UnitP Value†
    dRBC AdRBC BsRBCdRBC A v dRBC BsRBC v dRBC
    Abbreviations: dRBC A = Unit A of the Double Red Blood Cell Collection, dRBC B = Unit B of the Double Red Blood Cell Collection, sRBC = Single Red Blood Cell Unit, SD = Standard Deviation
    *
    All outcome measures are shown after 42 days of storage in AS-3 solution.
    †
    All comparisons were performed using a Student's T-test. A 2-tailed paired comparison was performed for dRBC A v dRBC B. A 2- tailed, two sample, equal variance comparison was performed for sRBC v dRBC units.
    ‡
    Osmotic fragility was measured as percent hemolysis in 0.55% saline at Site 1 and as the percent saline at ≥ 50% hemolysis at Site 2.
    Hematocrit (%), mean (SD)Site 154.4 (3.7)53.9 (3.6)55.8 (4.4)0.1320.253
    Site 256.0 (3.9)53.3 (11.6)58.4 (3.6)0.3980.149
    pH, mean (SD)Site 16.4 (0.04)6.4 (0.05)6.5 (0.08)0.7600.643
    Site 26.4 (0.1)6.4 (0.1)6.4 (0.1)0.1750.217
    pCO2, mean (SD)Site 1140 (8)137 (8)139 (12)0.1720.525
    Site 2130.5 (11.7)130.4 (12.4)125.6 (11.1)1.000.316
    pO2, mean (SD)Site 146 (7)47 (7)46 (7)0.1040.825
    Site 252.0 (10.6)51.4 (12.5)46.2 (3.4)0.8780.157
    ATP (μmols/g HB), mean (SD)Site 12.6 (0.6)2.6 (0.6)2.9 (0.5)0.7590.306
    Site 23.0 (0.5)3.0 (0.6)2.6 (0.5)0.8450.110
    K (mEq/L), mean (SD)Site 146.5 (7.9)47.5 (8.2)49.3 (10.1)0.3960.620
    Site 240.5 (5.8)41.1 (5.9)44.7 (5.7)0.5750.128
    Na (mEq/L), mean (SD)Site 1122 (7)123 (6)126 (17)0.0160.609
    Site 2105.6 (5.4)104.2 (5.5)100.0 (5.5)0.0040.069
    Total Hemoglobin (g/dL)Site 160.5 (5.8)60.0 (5.3)61.0 (4.7)0.5460.627
    Site 258.5 (5.5)59.6 (5.8)60.3 (5.0)0.2640.747
    Plasma Hemoglobin (mg/dL), mean (SD)Site 1149.9 (151.6)141.2 (145.3)152.7 (86.3)0.0340.815
    Site 2139.0 (61.0)126.7 (80.4)135.5 (82.1)0.2410.790
    Hemolysis (%), mean (SD)Site 10.33 (0.34)0.32 (0.34)0.30 (0.15)0.050.855
    Site 20.34 (0.13)0.31 (0.16)0.31 (0.19)0.3630.995
    Osmotic Fragility‡Site 120.0 (14.4)19.6 (15.2)31.0 (22.3)0.8850.152
    Site 20.51 (0.03)0.51 (0.03)0.49 (0.02)0.9350.009

    The primary outcome of this study was to demonstrate RBC collection, storage, and viability in vitro.

    The sRBC and dRBC units collected were comparable. The hematocrits, blood gasses, ATP, potassium, total hemoglobin, and osmotic fragility were within acceptable ranges following storage. Two statistically significant differences were identified between the A and B units in the dRBC collection at Day 42 (sodium and plasma free hemoglobin), but these differences were not clinically significant. There was no difference between dRBC units in hemolysis following storage in ADDITIVE SOLUTION FORMULA 3 (AS-3). A statistically significant difference was identified in the osmotic fragility of RBCs stored in ADDITIVE SOLUTION FORMULA 3 (AS-3) following sRBC collection or dRBC collection at Day 42, but the difference was not clinically significant. All the RBC units collected averaged less than 1% hemolysis on Day 42. These results are consistent with US and European guidelines for hemolysis on transfusion. ATP recovery was greater than 70% of all units, which is predictive of good in vivo viability, and potassium levels on Day 42 average less than 50 mEq/L indicating good RBC membrane stability over the storage period.

  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    ADDITIVE SOLUTION FORMULA 3 (AS-3) is a clear solution supplied in sterile and non-pyrogenic Polyolefin bags.

    SIZECATALOG NUMBERNDC NUMBERQUANTITY PER CASE
    100 mL4082414537-824-1036
    200 mL4082614537-826-2030
    350 mL4082814537-828-3524

    STORAGE

    Up to 25 °C.

    Protect from freezing.

  • SPL UNCLASSIFIED SECTION

    Issued: July 18, 2018

    Manufactured by
    Terumo BCT, Inc.
    Lakewood, CO 80215

  • PRINCIPAL DISPLAY PANEL - 100 mL Bag Pouch Carton Label

    Additive Solution Formula 3 (AS-3)

    Catalog # 40824 Polyolefin Bag 6 X 6 X 100 mL units
    NDC 14537-824-10

    Use only with Trima Accel red blood cell apheresis collections.
    See apheresis device operator's manual for complete instructions.
    Read the package insert before use.
    Sterile. Non-pyrogenic. Sterilized with steam.
    Caution: Do not use if the bag is damaged.
    Use only if solution is clear and free of particulate matter.
    Single use bag. Discard any unused product.
    Not for direct intravenous infusion. Rx Only.
    Recommended storage: Up to 25 °C. Protect from freezing.
    Protect from light.
    Each 100 mL contains:
    Dextrose Monohydrate USP
    1.10 g
    Trisodium Citrate Dihydrate USP
    0.588 g
    Sodium Chloride USP
    0.410 g
    Monobasic Sodium Phosphate Monohydrate USP
    0.276 g
    Citric Acid Monohydrate USP
    0.042 g
    Adenine USP
    0.030 g
    In Water for Injection USP

    Manufactured by Terumo BCT, Inc.
    TERUMOBCT
    10811 W. Collins Ave., Lakewood CO 80215, USA
    777965-076

    Lot
    Expiry Date

    PRINCIPAL DISPLAY PANEL - 100 mL Bag Pouch Carton Label
  • PRINCIPAL DISPLAY PANEL - 200 mL Bag Carton Label

    Additive Solution Formula 3 (AS-3)

    Catalog # 40826 Polyolefin Bag 30 X 200 mL units
    NDC 14537-826-20

    Use only with Trima Accel red blood cell apheresis collections.
    See apheresis device operator's manual for complete instructions.
    Read the package insert before use.
    Sterile. Non-pyrogenic. Sterilized with steam.
    Caution: Do not use if the bag is damaged.
    Use only if solution is clear and free of particulate matter.
    Single use bag. Discard any unused product.
    Not for direct intravenous infusion. Rx Only.
    Recommended storage: Up to 25 °C. Protect from freezing.
    Protect from light.
    Each 100 mL contains:
    Dextrose Monohydrate USP
    1.10 g
    Trisodium Citrate Dihydrate USP
    0.588 g
    Sodium Chloride USP
    0.410 g
    Monobasic Sodium Phosphate Monohydrate USP
    0.276 g
    Citric Acid Monohydrate USP
    0.042 g
    Adenine USP
    0.030 g
    In Water for Injection USP

    Manufactured by Terumo BCT, Inc.
    TERUMOBCT
    10811 W. Collins Ave., Lakewood CO 80215, USA
    777965-078

    Lot
    Expiry Date

    PRINCIPAL DISPLAY PANEL - 200 mL Bag Carton Label
  • PRINCIPAL DISPLAY PANEL - 350 mL Bag Carton Label

    Additive Solution Formula 3 (AS-3)

    Catalog # 40828 Polyolefin Bag 24 X 350 mL units
    NDC 14537-828-35

    Use only with Trima Accel red blood cell apheresis collections.
    See apheresis device operator's manual for complete instructions.
    Read the package insert before use.
    Sterile. Non-pyrogenic. Sterilized with steam.
    Caution: Do not use if the bag is damaged.
    Use only if solution is clear and free of particulate matter.
    Single use bag. Discard any unused product.
    Not for direct intravenous infusion. Rx Only.
    Recommended storage: Up to 25 °C. Protect from freezing.
    Protect from light.
    Each 100 mL contains:
    Dextrose Monohydrate USP
    1.10 g
    Trisodium Citrate Dihydrate USP
    0.588 g
    Sodium Chloride USP
    0.410 g
    Monobasic Sodium Phosphate Monohydrate USP
    0.276 g
    Citric Acid Monohydrate USP
    0.042 g
    Adenine USP
    0.030 g
    In Water for Injection USP

    Manufactured by Terumo BCT, Inc.
    TERUMOBCT

    10811 W. Collins Ave., Lakewood CO 80215, USA
    777965-080

    Lot
    Expiry Date

    PRINCIPAL DISPLAY PANEL - 350 mL Bag Carton Label
  • INGREDIENTS AND APPEARANCE
    ADDITIVE FORMULA 3 
    dextrose monohydrate, trisodium citrate dihydrate, sodium chloride, sodium phosphate, monobasic, monohydrate, citric acid monohydrate, and adenine solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:14537-824
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Dextrose Monohydrate (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) Dextrose Monohydrate1.1 g  in 100 mL
    Trisodium Citrate Dihydrate (UNII: B22547B95K) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID0.59 g  in 100 mL
    Sodium Chloride (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698, SODIUM CATION - UNII:LYR4M0NH37) Sodium Chloride0.41 g  in 100 mL
    SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN) (PHOSPHATE ION - UNII:NK08V8K8HR, SODIUM CATION - UNII:LYR4M0NH37) SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE0.28 g  in 100 mL
    Citric Acid Monohydrate (UNII: 2968PHW8QP) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID0.042 g  in 100 mL
    Adenine (UNII: JAC85A2161) (Adenine - UNII:JAC85A2161) Adenine0.03 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:14537-824-106 in 1 CARTON
    16 in 1 POUCH
    1100 mL in 1 BAG; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDABN00121405/29/2002
    ADDITIVE FORMULA 3 
    dextrose monohydrate, trisodium citrate dihydrate, sodium chloride, sodium phosphate, monobasic, monohydrate, citric acid monohydrate, and adenine solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:14537-826
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Dextrose Monohydrate (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) Dextrose Monohydrate1.1 g  in 100 mL
    Trisodium Citrate Dihydrate (UNII: B22547B95K) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID0.59 g  in 100 mL
    Sodium Chloride (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698, SODIUM CATION - UNII:LYR4M0NH37) Sodium Chloride0.41 g  in 100 mL
    SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN) (PHOSPHATE ION - UNII:NK08V8K8HR, SODIUM CATION - UNII:LYR4M0NH37) SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE0.28 g  in 100 mL
    Citric Acid Monohydrate (UNII: 2968PHW8QP) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID0.042 g  in 100 mL
    Adenine (UNII: JAC85A2161) (Adenine - UNII:JAC85A2161) Adenine0.03 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:14537-826-2030 in 1 CARTON
    1200 mL in 1 BAG; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDABN00121405/29/2002
    ADDITIVE FORMULA 3 
    dextrose monohydrate, trisodium citrate dihydrate, sodium chloride, sodium phosphate, monobasic, monohydrate, citric acid monohydrate, and adenine solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:14537-828
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Dextrose Monohydrate (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) Dextrose Monohydrate1.1 g  in 100 mL
    Trisodium Citrate Dihydrate (UNII: B22547B95K) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID0.59 g  in 100 mL
    Sodium Chloride (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698, SODIUM CATION - UNII:LYR4M0NH37) Sodium Chloride0.41 g  in 100 mL
    SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN) (PHOSPHATE ION - UNII:NK08V8K8HR, SODIUM CATION - UNII:LYR4M0NH37) SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE0.28 g  in 100 mL
    Citric Acid Monohydrate (UNII: 2968PHW8QP) (ANHYDROUS CITRIC ACID - UNII:XF417D3PSL) ANHYDROUS CITRIC ACID0.042 g  in 100 mL
    Adenine (UNII: JAC85A2161) (Adenine - UNII:JAC85A2161) Adenine0.03 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:14537-828-3524 in 1 CARTON
    1350 mL in 1 BAG; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDABN00121405/29/2002
    Labeler - Terumo BCT, Ltd (233649834)
    Establishment
    NameAddressID/FEIBusiness Operations
    Terumo BCT, Ltd233649834LABEL(14537-824, 14537-826, 14537-828) , ANALYSIS(14537-824, 14537-826, 14537-828) , STERILIZE(14537-824, 14537-826, 14537-828) , MANUFACTURE(14537-824, 14537-826, 14537-828)
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