CLEARASIL DAILY CLEAR  DAILY FACIAL SCRUB- salicylic acid lotion 
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®
Daily Facial Scrub

Drug Facts

Active ingredient

Salicylic acid 2%

Purpose

Acne medication

Use

for the treatment of acne

Warnings

For external use only

When using this product

  • avoid contact with the eyes. If product gets into the eyes, rinse thoroughly with water.
  • 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.
  • limit use to the face and neck

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, sodium laureth sulfate, polyethylene, propylene glycol, polyacrylate-1 crosspolymer, cocamidopropyl betaine, fragrance, sorbitol, sodium chloride, citric acid, polyquaternium 43, phenoxyethanol, sodium benzoate, FD&C blue no. 1 lake

Questions?

Call 1-866-25-CLEAR (1-866-252-5327).

Distributed by: Reckitt Benckiser LLC
Parsippany, NJ 07054-0224

PRINCIPAL DISPLAY PANEL - 150 mL Tube Label

Clearasil®

DAILY CLEAR®

Daily Facial
Scrub

Salicylic Acid 2% Acne Medication

With dual action
micro-beads.
Helps leave skin
soft and smooth.
Clearer skin everyday

5 FL OZ (150 mL)

PRINCIPAL DISPLAY PANEL - 150 mL Tube Label
CLEARASIL DAILY CLEAR   DAILY FACIAL SCRUB
salicylic acid lotion
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:63824-304
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 2 g  in 100 mL
Inactive Ingredients
Ingredient Name Strength
water (UNII: 059QF0KO0R)  
sodium laureth sulfate (UNII: BPV390UAP0)  
high density polyethylene (UNII: UG00KM4WR7)  
propylene glycol (UNII: 6DC9Q167V3)  
cocamidopropyl betaine (UNII: 5OCF3O11KX)  
sorbitol (UNII: 506T60A25R)  
sodium chloride (UNII: 451W47IQ8X)  
citric acid monohydrate (UNII: 2968PHW8QP)  
phenoxyethanol (UNII: HIE492ZZ3T)  
sodium benzoate (UNII: OJ245FE5EU)  
FD&C blue no. 1 (UNII: H3R47K3TBD)  
aluminum oxide (UNII: LMI26O6933)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:63824-304-65 150 mL in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH FINAL part333D 09/25/2012
Labeler - Reckitt Benckiser LLC (094405024)

Revised: 9/2012
Document Id: 5e39f3cf-53e7-423d-bac0-93920a53a617
Set id: fcb6b968-08ab-40d9-80cd-bc05287f12e0
Version: 1
Effective Time: 20120928
 
Reckitt Benckiser LLC