ACNE CLEANSER  - benzoyl peroxide lotion 
University Medical Pharmaceutical Corp

----------

LABEL for OIL-FREE ACNE CLEANSER 8 OZ

DO NOT USE

• IF YOU ARE SENSITIVE TO BENZOYL PEROXIDE OR HAVE VERY SENSITIVE SKIN. THIS PRODUCT MAY CAUSE IRRITATION.
  

WHEN USING THIS PRODUCT

• AVOID CONTACT WITH EYES. IF CONTACT OCCURS, FLUSH THOROUGHLY WITH WATER. KEEP AWAY FROM LIPS AND MOUTH.
• AVOID UNNECESSARY SUN EXPOSURE AND USE A SUNSCREEN.
• AVOID CONTACT WITH HAIR AND DYED FABRICS, INCLUDING CARPETS AND CLOTHING WHICH MAY BE BLEACHED BY THIS PRODUCT.
  

Water, Disodium Laureth Sulfosuccinate, Glyceryl Stearate, PEG-100 Stearate, Stearic Acid, Glycerin, Cocamidopropyl Betaine, Bakuchiol, Panthenyl Triacetate, Bisabolol, Benzalkonium Chloride, Chamomilla Recutita (Matricaria) Flower Extract, Naringenin, Sea Whip Extract, Polyrthylene, Xanthan Gum, Cetyl Alcohol, Magnesium Aluminum Silicate, Sodium Benzoate, Caprylic/Capric Triglycerides, Farnesol, Phenoxyethanol, Ethylhexylglycerin, Methylisothiazolinone.

USE FOR THE TREATMENT OF ACNE.

ACTIVE INGREDIENT
BENZOYL PEROXIDE 2.5% W/V

PURPOSE

ACNE TREATMENT

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

WARNINGS
FOR EXTERNAL USE ONLY.

DIRECTIONS
USE EVERY MORNING AND EVENING. APPLY A DIME-SIZE AMOUNT TO DAMP SKIN AND GENTLY MASSAGE, AVOIDING THE EYE AREA. RINSE WELL. IF BOTHERSOME PEELING OCCURS, REDUCE APPLICATION USE. MAY ALSO BE USED ON CHEST OR BACK.

STOP USE AND ASK A DOCTOR IF EXCESSIVE IRRITATION OCCURS.

ASK A DOCTOR OR PHARMACIST BEFORE USE

• IF YOU ARE USING OTHER TOPICAL ACNE DRUGS AT THE SAME TIME OR RIGHT AFTER USE OF THIS PRODUCT. THIS MAY INCREASE DRYNESS, REDNESS OR IRRITATION OF THE SKIN. IF THIS OCCURS, ONLY ONE MEDICATION SHOULD BE USED UNLESS A DOCTOR DIRECTS OTHERWISE.
  

AcneFree (R)
Clear Skin Treatments
Oil-Free
Acne
Cleanser

Gentle Exfoliating
MICROBEADS

ACNE CLEANSER  benzoyl peroxide   lotion

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 50544-1018 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOYL PEROXIDE (BENZOYL PEROXIDE) BENZOYL PEROXIDE 2.5 mg  in 1 mL

Inactive Ingredients Ingredient Name Strength WATER   DISODIUM LAURETH SULFOSUCCINATE   STEARIC ACID   GLYCERYL MONOSTEARATE   POLYOXYL 100 STEARATE   GLYCERIN   CETYL ALCOHOL   COCAMIDOPROPYL BETAINE   PANTHENOL   MATRICARIA RECUTITA   LEVOMENOL   BENZALKONIUM CHLORIDE   NARINGIN   PSEUDOPTEROGORGIA ELISABETHAE   PHENOXYETHANOL   ETHYLHEXYLGLYCERIN   MAGNESIUM ALUMINUM SILICATE   SODIUM BENZOATE   MEDIUM-CHAIN TRIGLYCERIDES   XANTHAN GUM   FARNESOL   METHYLISOTHIAZOLINONE   HIGH DENSITY POLYETHYLENE

Product Characteristics Color      Score      Shape Size Flavor Imprint Code Contains

Packaging # NDC Package Description Multilevel Packaging 1 50544-1018-1 237 mL In 1 BOTTLE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	09/28/2010

Labeler - University Medical Pharmaceutical Corp (809706252)

Registrant - University Medical Pharmaceutical Corp (809706252)

Establishment
Name	Address	ID/FEI	Operations
Universal Packaging Systems, Inc		177711082	manufacture

Establishment
Name	Address	ID/FEI	Operations
Micro Quality Labs Inc		149592615	analysis

Revised: 04/2011University Medical Pharmaceutical Corp