LA PRAIRIE CELLULAR BLEMISH CONTROL- salicylic acid gel 
La Prairie, Inc.

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.

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La Prairie Cellular Blemish Control

Active Ingredients                        
Salicylic Acid 2.0%...................

Purpose

Acne Treatment

Uses: - treats acne - clears acne blemishes - helps prevent the development of new acne blemishes

Warnings: For external use only - use other topical acne medication at the same time or immediately following the use of this product may increase should be used unless directed by a doctor.

Keep out of reach of children - if swallowed, get medical help or contact a Poison Control Center right away. - avoid contact with eyes

Directions: - cleanse skin thoroughly before applying - apply a thin layer to the blemish occurs, reduce application to once a day or every other day

  • Inactive Ingredients: SD Alcohol 40-B (Alcohol Denat.), Water (Aqua), Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Glycerin, Butylene Glycol, Hamamelis Virginiana (Witch Hazel) Extract, Betula Alba (Birch) Bark Extract, Arctium Lappa (Burdock) Root Extract, Cupressus Sempervirens (Cypress) Leaf Extract, Lamium Album Flower (White Nettle) Flower Extract, Salvia Officinalis  (Sage) Leaf Extract, Benzalkonium Chloride, PEG-8, Alpha-Glucan Oligasaccharide, Melia Azadirachta (Neem) Leaf Extract, Hydrolyzed Milk Protein, Glucose Oxidase, Lactoperoxidase, Lactoferrin, Potassium Thiocyanate, Glycoproteins, Panax Ginseng Root Extract, Equisetum Arvense (Horesetail) Extract, Glucose Pentaacetate, Lacithin, Caprylyl Glycol, Avena Sativa (Oat) Meal Extract, Sebacic Acid, Sodium Polyacrylate, Propylene Glycol, Fragrance (Parfum), (i09) *La Prairie’s exclusive Cellular Complex US Patent 5,840,309

Blemish Control 1

Blemish Control 2

LA PRAIRIE CELLULAR BLEMISH CONTROL 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68026-311
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SAGE (UNII: 065C5D077J)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
.ALPHA.-GLUCAN OLIGOSACCHARIDE (UNII: S95658MI3W)  
GLUCOSE OXIDASE (UNII: 0T8392U5N1)  
POTASSIUM THIOCYANATE (UNII: TM7213864A)  
ASIAN GINSENG (UNII: CUQ3A77YXI)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
SEBACIC ACID (UNII: 97AN39ICTC)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68026-311-1515 mL in 1 BOTTLE; Type 0: Not a Combination Product04/17/201110/17/2013
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D04/17/201110/17/2013
Labeler - La Prairie, Inc. (092848621)

Revised: 5/2016
 
La Prairie, Inc.