Label: NEUTROGENA STUBBORN BLACKHEADS DAILY SERUM- salicylic acid lotion

  • NDC Code(s): 69968-0703-1, 69968-0703-2
  • Packager: Kenvue Brands LLC
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 12, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Salicylic Acid 0.5%

  • Purpose

    Acne treatment

  • Use

    • For the treatment of acne
    • Penetrates pores to eliminate most blackheads.
  • Warnings

    For external use only.

    When using this product

    • Avoid contact with eyes. If contact occurs, immediately flush with water.
    • 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.

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Clean the skin thoroughly before applying this product.
    • Cover the entire affected area with a thin layer one to three times daily.
    • Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.
    • If bothersome dryness or peeling occurs, reduce application to once a day or every other day.
  • Inactive ingredients

    Water, Propylene Glycol, Glycolic Acid, Dimethicone, Mandelic Acid, Gluconolactone, Sodium Hydroxide, Neopentyl Glycol Diheptanoate, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Polyacrylate Crosspolymer-6, Dimethicone Crosspolymer, Disodium EDTA

  • Other information

    • Store at room temperature.
    • Sunburn Alert: This product contains an alpha hydroxy 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.
  • Questions?

    800-582-4048; Outside US, dial collect 215-273-8755 or visit www.neutrogena.com

  • SPL UNCLASSIFIED SECTION

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

  • PRINCIPAL DISPLAY PANEL - 30 mL Tube Carton

    New
    Neutrogena ®
    DERMATOLOGIST
    RECOMMENDED BRAND

    STUBBORN
    BLACKHEADS
    DAILY SERUM
    Salicylic Acid Acne Treatment

    visibly clears clogged pores
    and helps eliminate blackheads

    10% Glycolic + Mandelic
    + Polyhydroxy Acids
    Fragrance-Free

    1.0 FL OZ (30mL)

    PRINCIPAL DISPLAY PANEL - 30 mL Tube Carton
  • INGREDIENTS AND APPEARANCE
    NEUTROGENA STUBBORN BLACKHEADS DAILY SERUM 
    salicylic acid lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0703
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    MANDELIC ACID (UNII: NH496X0UJX)  
    GLUCONOLACTONE (UNII: WQ29KQ9POT)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
    HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)  
    DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0703-11 in 1 CARTON08/02/2021
    130 mL in 1 TUBE; Type 0: Not a Combination Product
    2NDC:69968-0703-21 in 1 BLISTER PACK08/02/2021
    23.5 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00608/02/2021
    Labeler - Kenvue Brands LLC (118772437)
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