CLEAN AND CLEAR BLACKHEAD ERASER SCRUB- salicylic acid cream 
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.

----------

Clean & Clear® blackhead eraser® scrub

Drug Facts

Active ingredients

Salicylic Acid 2%

Purpose

Acne treatment

Uses

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

Other information

Store at Room Temperature.

Inactive ingredients

Water, Cetyl alcohol, PPG-15 Stearyl Ether, Cellulose, Glycerin, Polysorbate 60, Steareth-21, Microcrystalline Wax, Potassium Cetyl Phosphate, Xanthan Gum, Fragrance, Disodium EDTA, Methyl Lactate, Sodium Hydroxide, Ferric Ferrocyanide

Questions?

877-754-6411; Outside US, dial collect 215-273-8755 or visit www.CleanandClear.com

Distributed by:
JOHNSON & JOHNSON
CONSUMER INC.

Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 198 g Tube Label

VALUE

SIZE

Clean

&

Clear ®

blackhead

eraser ®


scrub

salicylic acid acne medication

OIL-FREE

reduces the number

of blackheads

gently exfoliates to

lift away dirt & oil

Johnson & Johnson

NET WT. 7 OZ. (198 g)

CC-001

CLEAN AND CLEAR BLACKHEAD ERASER SCRUB 
salicylic acid cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0234
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)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)  
STEARETH-21 (UNII: 53J3F32P58)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
GLYCERIN (UNII: PDC6A3C0OX)  
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
XANTHAN GUM (UNII: TTV12P4NEE)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
METHYL LACTATE, (-)- (UNII: 0379G9C44S)  
FERRIC FERROCYANIDE (UNII: TLE294X33A)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0234-5141 g in 1 TUBE; Type 0: Not a Combination Product06/01/2016
2NDC:69968-0234-7198 g in 1 TUBE; Type 0: Not a Combination Product06/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333D06/01/2016
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2023
Document Id: ee48b183-b39d-fcbf-e053-2a95a90a4bee
Set id: 20197516-ce6b-4ae9-81ee-fac7636f844a
Version: 6
Effective Time: 20230109
 
Johnson & Johnson Consumer Inc.