CLEARASIL  DAILY CLEAR VANISHING ACNE TREATMENT- benzoyl peroxide cream 
Reckitt Benckiser 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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Clearasil®
Daily Clear® Vanishing Acne Treatment Cream

Drug Facts

Active ingredient

Benzoyl peroxide 10%

Purpose

Acne medication

Use

for the treatment of acne

Warnings

For external use only

Do not use if you

  • have very sensitive skin
  • are sensitive to benzoyl peroxide

When using this product

  • avoid unnecessary sun exposure and use a sunscreen
  • avoid contact with the eyes, lips and mouth
  • avoid contact with hair and dyed fabrics, which may be bleached by 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.
  • skin irritation may occur, characterized by redness, burning, itching, peeling or possibly swelling. Irritation may be reduced by using the product less frequently or in a lower concentration.

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

Water, Propylene Glycol, Aluminium Hydroxide, Bentonite, Glyceryl Stearate SE, PEG-12, Isopropyl Myristate, Methylparaben, Carbomer, Potassium Hydroxide, Propylparaben

Questions?

Call 1-866-25-CLEAR (1-866-252-5327). You may also report side effects to this phone number.

Distributed by: Reckitt Benckiser LLC
Parsippany, NJ 07054-0224
Made in USA © RB 2011

PRINCIPAL DISPLAY PANEL - 28 g Tube Carton

Clearasil®

DAILY CLEAR®

Vanishing Acne
Treatment Cream

Benzoyl Peroxide 10% Acne Medication

Principal Display Panel - 28 g Tube Carton
CLEARASIL   DAILY CLEAR VANISHING ACNE TREATMENT
benzoyl peroxide cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:63824-303
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Benzoyl Peroxide (UNII: W9WZN9A0GM) (Benzoyl Peroxide - UNII:W9WZN9A0GM) Benzoyl Peroxide 10 g  in 100 g
Inactive Ingredients
Ingredient Name Strength
Water (UNII: 059QF0KO0R)  
Propylene Glycol (UNII: 6DC9Q167V3)  
Aluminum Hydroxide (UNII: 5QB0T2IUN0)  
Bentonite (UNII: A3N5ZCN45C)  
Glyceryl Stearate SE (UNII: FCZ5MH785I)  
Polyethylene Glycol 600 (UNII: NL4J9F21N9)  
Isopropyl Myristate (UNII: 0RE8K4LNJS)  
Methylparaben (UNII: A2I8C7HI9T)  
Potassium Hydroxide (UNII: WZH3C48M4T)  
Propylparaben (UNII: Z8IX2SC1OH)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63824-303-02 1 in 1 CARTON
1 28 g in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH FINAL part333D 09/01/2011
Labeler - Reckitt Benckiser LLC (094405024)

Revised: 11/2012
Document Id: 306ed258-1dfb-4b1b-8aff-65c81b7dd6f7
Set id: dd074b97-e09b-48a5-bd86-f11934abd897
Version: 2
Effective Time: 20121108
 
Reckitt Benckiser LLC