Label: NEUTROGENA ALL IN 1 ACNE CONTROL DAILY SCRUB- salicylic acid liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 11, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Salicylic Acid 2%

  • Purpose

    Acne treatment

  • Use

    For the treatment of acne.

  • 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

    Cleanse twice a day. Wet face. Apply to hands, add water and work into a lather. Massage face gently. Rinse thoroughly.

  • Other Information

    Store at Room Temperature.

  • Inactive ingredients

    water, cetyl alcohol, PPG-15 stearyl ether, cellulose, glycerin, Polysorbate 60, steareth-21, potassium cetyl phosphate, xanthan gum, fragrance, disodium EDTA, menthyl lactate, sodium hydroxide

  • Questions?

    Call toll- free 800-582-4048 or 215-273-8755 (collect). www.neutrogena.com

  • SPL UNCLASSIFIED SECTION

    Distributed by:
    JOHNSON AND JOHNSON CONSUMER INC.
    Skillman, NJ 08558

  • PRINCIPAL DISPLAY PANEL - 124 mL Tube Label

    NEW &
    IMPROVED

    All-in-1
    Acne
    Control
    daily scrub

    works on acne's
    past, present & future

    • exfoliates past acne marks
    • clears present breakouts
    • helps prevent future breakouts

    Neutrogena ®

    salicylic acid acne treatment

    4.2 FL. OZ. (124mL)

    PRINCIPAL DISPLAY PANEL - 124 mL Tube Label
  • INGREDIENTS AND APPEARANCE
    NEUTROGENA ALL IN 1 ACNE CONTROL DAILY SCRUB 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0092
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)  
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    STEARETH-21 (UNII: 53J3F32P58)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0092-4124 mL in 1 TUBE; Type 0: Not a Combination Product06/01/2016
    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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