Label: NEUTROGENA OIL FREE ACNE WASH PINK GRAPEFRUIT FOAMING SCRUB- salicylic acid gel

  • NDC Code(s): 69968-0610-2, 69968-0610-4, 69968-0610-7
  • Packager: Johnson & Johnson Consumer Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated August 28, 2024

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  • 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 and work into a lather.
    • Massage face gently.
    • Rinse thoroughly.
  • Other information

    Store at Room Temperature

  • Inactive ingredients

    Water, Sodium C14-16 Olefin Sulfonate, Glycerin, Cocamidopropyl Betaine, Microcrystalline Cellulose, Sodium Chloride, Acrylates Copolymer, Cellulose, Polysorbate 20, Fragrance, C12-15 Alkyl Lactate, Sodium Hydroxide, Disodium EDTA, Benzalkonium Chloride, Polyquaternium-7, Cocamidopropyl PG-Dimonium Chloride Phosphate, Sodium Benzotriazolyl Butylphenol Sulfonate, Propylene Glycol, Citrus Grandis (Grapefruit) Fruit Extract, Carrageenan, Agar, Ascorbyl Palmitate, Mica, Titanium Dioxide, Red 30, Red 40, Violet 2

  • 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

  • PRINCIPAL DISPLAY PANEL - 198 mL Tube Label

    VALUE SIZE

    Oil-Free

    Acne Wash

    pink grape fruit

    foaming scrub

    MICRO CLEAR ®

    technology

    clear breakouts

    naturally derived grapefruit extract

    Neutrogena ®

    salicylic acid acne treatment

    6.7 FL. OZ. (198 mL)

    Ntg_001

  • INGREDIENTS AND APPEARANCE
    NEUTROGENA OIL FREE ACNE WASH PINK GRAPEFRUIT FOAMING SCRUB 
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0610
    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
    ASCORBYL PALMITATE (UNII: QN83US2B0N)  
    MICA (UNII: V8A1AW0880)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    D&C RED NO. 30 (UNII: 2S42T2808B)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    D&C VIOLET NO. 2 (UNII: 350KA7O6HK)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)  
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    C12-15 ALKYL LACTATE (UNII: GC844VRD7E)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)  
    COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
    SODIUM BENZOTRIAZOLYL BUTYLPHENOL SULFONATE (UNII: 0LA2QC9O3Z)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PUMMELO (UNII: ET1TN5W71X)  
    CARRAGEENAN (UNII: 5C69YCD2YJ)  
    AGAR, UNSPECIFIED (UNII: 89T13OHQ2B)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0610-7198 mL in 1 TUBE; Type 0: Not a Combination Product12/30/2019
    2NDC:69968-0610-4124 mL in 1 TUBE; Type 0: Not a Combination Product12/30/2019
    3NDC:69968-0610-259 mL in 1 TUBE; Type 0: Not a Combination Product12/09/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00612/09/2019
    Labeler - Johnson & Johnson Consumer Inc. (118772437)
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