CLENZIDERM DAILY CARE FOAMING CLEANSER ACNE TREATMENT- salicylic acid liquid 
Bausch Health US LLC

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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CLENZIDERM M.D.
DAILY CARE
FOAMING CLEANSER

DRUG FACTS

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

skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.

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

Cleanse the entire affected area with a thin layer and rinse thoroughly one to three times daily.
Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.
If bothersome dryness or peeling occurs, reduce application to once a day or every other day.

Other Information

Store away from heat and direct sunlight.
Store at controlled room temperature: 15°C-25°C (59°F-77°F).

Inactive Ingredients

butyl avocadate, cetyl hydroxyethylcellulose, cocamidopropyl betaine, disodium EDTA, ethoxydiglycol, ext. D&C Violet 2, fragrance, menthol, menthyl lactate, sodium laureth sulfate, sodium lauryl sulfate, water

Questions or comments?

1.800.636.7546 Monday-Friday 9a.m.-4p.m. Pacific Time

PRINCIPAL DISPLAY PANEL - 118 mL Bottle Label

OBAGI®

MEDICAL

CLENZIderm M.D.™

Daily Care Foaming Cleanser

Salicylic Acid 2%
Acne Treatment

4 fl. oz. (118 mL)

Clenziderm M.D. Daily Care Foaming Cleanser 118 mL Bottle Label
CLENZIDERM DAILY CARE FOAMING CLEANSER  ACNE TREATMENT
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0187-6100
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)  
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)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
ColorPURPLEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0187-6100-04118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/02/201508/01/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D03/02/201508/01/2017
Labeler - Bausch Health US LLC (831922468)

Revised: 5/2015
 
Bausch Health US LLC