Label: CLEAN AND CLEAR BLACKHEAD ERASER SCRUB- salicylic acid cream

  • NDC Code(s): 69968-0234-5, 69968-0234-7
  • Packager: Kenvue Brands LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 11, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredients

    Salicylic Acid 2%

  • Purpose

    Acne treatment

  • Uses

    • for the treatment of acne
    • clears blackheads
  • 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.
    • Gently massage all over face for 20-30 seconds, avoiding eye area.
    • Rinse thoroughly and pat dry.
    • Recommended for daily use.
  • 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

  • SPL UNCLASSIFIED SECTION

    Distributed by:
    Kenvue Brands LLC
    Summit, NJ 07901

  • 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

    NET WT. 7 OZ. (198 g)

    Clean and Clear_1

  • INGREDIENTS AND APPEARANCE
    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 DrugM00606/01/2016
    Labeler - Kenvue Brands LLC (118772437)
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