Label: NEUTROGENA OIL-FREE ACNE WASH DAILY SCRUB- salicylic acid gel

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 11, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredients

    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.
    • Massage face gently.
    • Rinse thoroughly.
  • Other information

    • Sunburn Alert

      This product contains an alpha hydroxyl acid (AHA) that may increase your skin's sensitivity to the sun and particularly the possibility of sunburn. Use a sunscreen, wear protective clothing and limit sun exposure while using this product and for a week afterwards. Store at Room Temperature.

  • Inactive ingredients

    water, cetyl alcohol, PPG-15 stearyl ether, cellulose, glycerin, Polysorbate 60, steareth-21, C12-15 alkyl lactate, glycolic acid, cetyl lactate, potassium cetyl phosphate, sodium hydroxide, xanthan gum, cocamedopropyl PG-dimonium chloride phosphate, disodium EDTA, fragrance, menthol, Benzalkonium chloride, agar, BHT, sodium benzotriazolyl, butylphenone sulfonate, iron oxides, mica, yellow 5, titanium dioxide, red 30, red 40

  • Questions?

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

  • SPL UNCLASSIFIED SECTION

    Distributed by:
    JOHNSON & JOHNSON CONSUMER INC.
    Skillman, NJ 08558
    J&JCI2016

  • PRINCIPAL DISPLAY PANEL - 124 mL Tube Label

    Oil-Free
    Acne Wash

    Daily Scrub
    MICRO CLEAR ®
    technology

    multi-action scrub helps stop
    breakouts before they start

    Neutrogena ®

    salicylic acid acne treatment
    4.2 FL.OZ.(124mL)

    PRINCIPAL DISPLAY PANEL - 124 mL Tube Label
  • INGREDIENTS AND APPEARANCE
    NEUTROGENA OIL-FREE ACNE WASH DAILY SCRUB 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0075
    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)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    C12-15 ALKYL LACTATE (UNII: GC844VRD7E)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    CETYL LACTATE (UNII: A7EVH2RK4O)  
    POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    AGAR, UNSPECIFIED (UNII: 89T13OHQ2B)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    MICA (UNII: V8A1AW0880)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    D&C RED NO. 30 (UNII: 2S42T2808B)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0075-4124 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)