Label: NEUTROGENA BODY CLEAR BODY SCRUB- salicylic acid suspension

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

Drug Label Information

Updated November 12, 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

    Use daily in the shower or bath.

    • For maximum lather, massage over wet skin with a washcloth or body puff, concentrating on areas prone to breakouts.
    • Rinse well.
  • Other information

    Store at Room Temperature.

  • Inactive ingredients

    Water, Sodium C14-16 Olefin Sulfonate, Glycerin, Cocamidopropyl Betaine, Microcrystalline Cellulose, Sodium Chloride, Acrylates Copolymer, Cellulose, Fragrance, Sodium Hydroxide, Disodium EDTA, Aloe Barbadensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Yellow 6, Yellow 5, Red 40, Red 33, Blue 1

  • 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 - 250 mL Bottle Label

    Body
    Clear ®
    Body Scrub

    treats and helps prevent
    body breakouts for
    smooth, clear skin

    with aloe and chamomile

    salicylic acid acne treatment

    Neutrogena ®
    DERMATOLOGIST RECOMMENDED

    8.5 FL. OZ. (250 mL)

    Principal Display Panel - 250 mL Bottle Label
  • INGREDIENTS AND APPEARANCE
    NEUTROGENA BODY CLEAR BODY SCRUB 
    salicylic acid suspension
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0628
    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)  
    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)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CHAMOMILE (UNII: FGL3685T2X)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0628-9250 mL in 1 BOTTLE; Type 0: Not a Combination Product02/24/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00602/24/2020
    Labeler - Kenvue Brands LLC (118772437)
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