CLEAN AND CLEAR ACNE TRIPLE CLEAR EXFOLIATING SCRUB- salicylic acid gel 
Johnson & Johnson Consumer Inc.

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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Clean & Clear ® acne triple clear exfoliating scrub

Drug Facts

Active ingredient

Salicylic Acid (2%)

Purpose

Acne treatment

Use

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.
  • avoid contact with eyes. If contact occurs, flush thoroughly with water.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Wet face. Squeeze into hands. Apply to face and massage gently, avoiding eye area. Rinse thoroughly.

Other information

Store at Room Temperature

Inactive ingredients

Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Hydroxysultaine, Sorbitol, Cellulose, Sodium Hydrolyzed Potato Starch Dodecenylsuccinate, Acrylates Crosspolymer-4, Sodium Hydroxide, Fragrance, Microcrystalline Wax, Menthol, C12-15 Alkyl Lactate, Benzalkonium Chloride, Disodium EDTA, Glycerin, Cocamidopropyl PG-Dimonium Chloride Phosphate, Aloe Barbadensis Leaf Extract, Mentha Piperita (Peppermint) Leaf Extract, Ferric Ferrocyanide

Questions?

call toll-free 877-754-6411 or 215-273-8755 (collect) www.cleanandclear.com

Distributed by:
JOHNSON & JOHNSON
CONSUMER INC.

Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 141 g Tube Label

NEW
Clean
&
Clear ®  ®

acne
triple clear
exfoliating scrub
salicylic acid acne treatment

OIL-FREE

gently exfoliates and fights
breakouts in 3 ways

cool, refreshing clean
aloe + mint

Johnson & Johnson

Net Wt. 5 Oz. (141 g)

PRINCIPAL DISPLAY PANEL - 141 g Tube Label
CLEAN AND CLEAR ACNE TRIPLE CLEAR EXFOLIATING SCRUB 
salicylic acid gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0013
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)  
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
GLYCERIN (UNII: PDC6A3C0OX)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
FERRIC FERROCYANIDE (UNII: TLE294X33A)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
MENTHA PIPERITA LEAF (UNII: A389O33LX6)  
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
C12-15 ALKYL LACTATE (UNII: GC844VRD7E)  
SORBITOL (UNII: 506T60A25R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0013-5141 g in 1 TUBE; Type 0: Not a Combination Product11/01/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D11/01/2016
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2023
Document Id: edf589c4-e913-5cfa-e053-2995a90ae311
Set id: fb15d9b4-386f-4be5-b39b-8e95c982dce7
Version: 6
Effective Time: 20230105
 
Johnson & Johnson Consumer Inc.