AF FOAM SENSITIVE ACNE PORE CLEANSER - salicylic acid aerosol, foam 
University Medical Pharmaceuticals Corp

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

AF Foam Sensitive Acne Pore Cleanser

Active ingredient: Salicylic Acid 1.5% w/v

Purpose: Acne Treatment

Use for the treatment of acne.

Warnings: For external use only

Do not use If you have a known allergy to Salicylic Acid or aspirin.
Using other topical acne medications at the same time or right after use of this product may increase drynes or irritation of the skin. If this occurs only one medication should be used unless directed by a doctor.

When using this product

Stop use and ask a doctor if excessive irritation occurs.

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

Directions

Other information

Inactive ingredients: Avena Sativa (Oat) Kernel Extract, Bisabolol, Cocamidopropyl Betaine, Disodium Laureth Sulfosuccinate, Glycerin, Methylisothiazolinone, Phenoxyethanol, Sodium Chloride, Sodium Hydroxide, Sodium C14-16 Olefin Sulfonate, Tetrasodium Glutamate Diacetate, Water/Aqua/Eau, Zinc PCA, Zingiber Officinale (Ginger) Root Extact.

AcneFree Sensitive

Gentle Formula
Acne Pore Cleanser
Salicylic Acid 1.5%

Rinse-Off Foam
Medicine Stays In Pores Even After Rinsing
Front Label
Drug Facts 1
Drug Facts 2
AF FOAM SENSITIVE ACNE PORE CLEANSER 
salicylic acid aerosol, foam
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50544-304
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
salicylic acid (UNII: O414PZ4LPZ) (Salicylic acid - UNII:O414PZ4LPZ) salicylic acid1.5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
oat (UNII: Z6J799EAJK)  
LEVOMENOL (UNII: 24WE03BX2T)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)  
glycerin (UNII: PDC6A3C0OX)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
water (UNII: 059QF0KO0R)  
ZINC PIDOLATE (UNII: C32PQ86DH4)  
ginger (UNII: C5529G5JPQ)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50544-304-4085 g in 1 CAN
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D11/15/2011
Labeler - University Medical Pharmaceuticals Corp (809706252)
Registrant - University Medical Pharmaceuticals Corp (809706252)

Revised: 12/2011
Document Id: a5c8f9f0-a6cd-4163-99ad-db2ba00fbd92
Set id: f08eb783-0bca-4bd1-9122-518742e92a79
Version: 3
Effective Time: 20111214
 
University Medical Pharmaceuticals Corp