ALL-DAY ACNE CONTROL  - benzoyl peroxide aerosol, foam 
University Medical Pharmaceutical Corp

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ALL-DAY ACNE CONTROL FOAM

DO NOT USE

WHEN USING THIS PRODUCT

INACTIVE INGREDIENTS: BAKUCHIOL, Benzalkonium Chloride, Bisabolol, BUTYLENE GLYCOL, C12-15 ALKYL BENZOATE, Caprylic/Capric Triglycerides, CETEARYL ALCOHOL, Chamomilla Recutita (Matricaria) Flower Extract, DIMETHICONE, Ethylhexylglycerin, Glycerin, Glyceryl Stearate, HYDROXYPROPYL STARCH PHOSPHATE, ISOBUTANE, METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER, Methylisothiazolinone, Naringenin, Panthenyl Triacetate, PEG-100 Stearate, Phenoxyethanol, POLYSORBATE 60, PROPANE, Sea Whip Extract, TETRASODIUM EDTA, Water, Xanthan Gum, ZINGIBER OFFICIANALE (GINGER) ROOT EXTRACT

USE FOR THE TREATMENT OF ACNE.

WARNINGS
FOR EXTERNAL USE ONLY.

Ask a doctor or a 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.

PURPOSE
ACNE TREATMENT

Directions:

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Stop use and ask a doctor if excessive skin irritation occurs.

ACTIVE INGREDIENT
BENZOYL PEROXIDE 5% W/V

ACNE FREE
CLEAR SKIN TREATMENTS

OIL-FREE
ALL-DAY ACNE
CONTROL
MICRO BENZOYL PEROXIDE 5%
LEAVE-ON
FOAM
AF Foam All-Day Acne Control ART 2011-04-08 LBL-DF1
AF Foam All-Day Acne Control ART 2011-04-08 LBL-DF2
AF Foam All-Day Acne Control ART 2011-04-08 LBL-Outer

ALL-DAY ACNE CONTROL 
benzoyl peroxide   aerosol, foam
Product Information
Product TypeHUMAN OTC DRUGNDC Product Code (Source)50544-3063
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZOYL PEROXIDE (BENZOYL PEROXIDE) BENZOYL PEROXIDE5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
BENZALKONIUM CHLORIDE 
LEVOMENOL 
BUTYLENE GLYCOL 
ALKYL (C12-15) BENZOATE 
MEDIUM-CHAIN TRIGLYCERIDES 
CETOSTEARYL ALCOHOL 
CETYL ALCOHOL 
CHAMOMILE 
DIMETHICONE 
ETHYLHEXYLGLYCERIN 
GLYCERIN 
GLYCERYL MONOSTEARATE 
HYDROXYPROPYL DISTARCH PHOSPHATE, HIGH AMYLOSE CORN 
ISOBUTANE 
METHYL METHACRYLATE 
GLYCOL DIMETHACRYLATE 
METHYLISOTHIAZOLINONE 
NARINGENIN 
PANTHENOL 
PEG-100 STEARATE 
PHENOXYETHANOL 
POLYSORBATE 60 
PROPANE 
PSEUDOPTEROGORGIA ELISABETHAE 
EDETATE SODIUM 
WATER 
XANTHAN GUM 
GINGER 
Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#NDCPackage DescriptionMultilevel Packaging
150544-3063-285 g In 1 CANNone

Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D03/29/2011

Labeler - University Medical Pharmaceutical Corp (809706252)
Registrant - University Medical Pharmaceutical Corp (809706252)
Establishment
NameAddressID/FEIOperations
Universal Packaging Systems, Inc177711082manufacture
Establishment
NameAddressID/FEIOperations
Micro Quality Labs Inc149592615analysis
Establishment
NameAddressID/FEIOperations
220 Laboratories Inc.783247950manufacture
Revised: 04/2011University Medical Pharmaceutical Corp