OBAGI- salicylic acid gel 
YS PLUS CORPORATION

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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Drug Facts

Inactive Ingredients

butyl avocadate, cetyl hydroxymethylcellulose, cocamidopropyl betaine, disodium

EDTA, ethoxydiglycol, Ext. Violet 2 ( CI 60730), fragrance, menthol, menthyl

lactate, sodium laureth sulfate, sodium lauryl sulfate, water (aqua)

Active Ingredient

Salicylic Acid 2 %

Purpose

Acne treatment gel

Uses

- for the treatment of acne

- dries up acne pimples

- helps prevent new acne pimples

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

- use AM and PM

- wet face

- gently massage product all over face for 20 - 30 seconds avoiding eye area

- rinse thoroughly and pat dry

- wait 10 - 15 minutes to allow skin to dry completely

Other information

- store away from heat and direct sunlight

- store at controlled room temperature: 15 C - 25 C (59 F - 77 F)

Questions or comments?  1.800.636.7546

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

copy of label
OBAGI 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69269-111
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
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, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)  
EXT. D&C VIOLET NO. 2 (UNII: G5UX3K0728)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69269-111-60118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/15/201412/31/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D10/15/201412/31/2015
Labeler - YS PLUS CORPORATION (843007597)

Revised: 10/2014
 
YS PLUS CORPORATION