CLENZIDERM DAILY CARE FOAMING CLEANSER ACNE TREATMENT

Dosage form: liquid
Ingredients: SALICYLIC ACID 20mg in 1mL
Labeler: OMP, INC.
NDC Code: 62032-111

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.

CLENZIDERM
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
  • 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°-25°C (59°-77°F).

Inactive Ingredients

Butyl Avocadate, Cetyl Hydroxyethylcellulose, Cocamidopropyl Betaine, Disodium EDTA, Ethoxydiglycol, Fragrance, Menthol, Menthyl Lactate, Sodium Laureth Sulfate, Sodium Lauryl Sulfate, Ext. Violet 2 (CI 60730), Water (Aqua).

Questions?

(800) 636-7546 Mon-Fri 9:00 am – 4:00 p.m. Pacific Time

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

PRINCIPAL DISPLAY PANEL - 118 mL Bottle Label

OBAGI®

CLENZIderm M.D.™

Daily Care
Foaming Cleanser

SALICYLIC ACID 2%
ACNE TREATMENT

1

Removes dirt
and excess
oil, leaving
skin clean
and refreshed.

4 FL.OZ. (118 mL)

CLENZIDERM DAILY CARE FOAMING CLEANSER   ACNE TREATMENT
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62032-111
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (SALICYLIC ACID) SALICYLIC ACID20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM LAURETH SULFATE 
DIETHYLENE GLYCOL MONOETHYL ETHER 
SODIUM LAURYL SULFATE 
COCAMIDOPROPYL BETAINE 
CETYL HYDROXYETHYLCELLULOSE (350000 MW) 
EDETATE DISODIUM 
MENTHOL 
MENTHYL LACTATE 
EXT. D&C VIOLET NO. 2 
WATER 
Product Characteristics
ColorPURPLEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:62032-111-60118 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart333D02/01/2007
Labeler - OMP, INC. (790553353)
Establishment
NameAddressID/FEIOperations
PURETEK CORPORATION785961046MANUFACTURE(62032-111), LABEL(62032-111), PACK(62032-111)
Establishment
NameAddressID/FEIOperations
Ei INC.105803274MANUFACTURE(62032-111), LABEL(62032-111), PACK(62032-111), ANALYSIS(62032-111)

Revised: 12/2011
 
OMP, INC.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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