DAILY CARE FOAMING CLEANSER  ACNE TREATMENT- salicylic acid liquid 
OMP, 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.

----------

DAILY CARE FOAMING CLEANSER
ACNE TREATMENT

Drug Facts

Active ingredient

Salicylic Acid 2%

Purpose

Acne treatment gel

Uses

Warnings

For external use only

When using this product

  • using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.

Stop use and ask a doctor if

  • irritation becomes severe

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

Directions

Other information

Inactive ingredients

butyl avocadate, cetyl hydroxyethylcellulose, cocamidopropyl betaine, disodium EDTA, ethoxydiglycol, Ext. Violet 2 (CI 60730), fragrance, menthol, menthyl lactate, sodium laureth sulfate, sodium lauryl sulfate, water (aqua)

Questions or comments?

1.800.636.7546

Monday–Friday 9 a.m.–4 p.m. Pacific Time

Distributed by OMP, Inc., Long Beach, CA 90806

PRINCIPAL DISPLAY PANEL - 1 L Bottle Label

FOR PROFESSIONAL USE ONLY

OBAGI®
MEDICAL

Daily Care
Foaming Cleanser

Salicylic Acid 2%
Acne Treatment

Removes dirt and excess oil,
leaving skin clean and refreshed

33.8 fl. oz. (1 L)

Principal Display Panel - 1 L Bottle Label
DAILY CARE FOAMING CLEANSER   ACNE TREATMENT
salicylic acid liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:62032-129
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
WATER (UNII: 059QF0KO0R)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
MENTHOL (UNII: L7T10EIP3A)  
MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)  
EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)  
Product Characteristics
Color PURPLE Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:62032-129-07 1000 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part333D 01/18/2013
Labeler - OMP, INC. (790553353)
Establishment
Name Address ID/FEI Business Operations
G.S. COSMECEUTICAL USA, INC. 017014734 MANUFACTURE(62032-129)

Revised: 3/2013
Document Id: db6fb272-6194-432d-a05c-7b87c11bd373
Set id: 5ce60534-bc66-4754-b858-a78968d4592c
Version: 1
Effective Time: 20130320
 
OMP, INC.