Label: NEUTROGENA SCALP THERAPY ANTI-DANDRUFF DAILY CONTROL- salicylic acid shampoo

  • 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 (1.8%)

  • Purposes

    Anti-dandruff, Anti-seborrheic dermatitis, Anti-psoriasis

  • Use

    Controls the symptoms of dandruff, seborrheic dermatitis and psoriasis.

  • Warnings

    • For external use only.

    • Ask a doctor before use if you have a condition that covers a large area of the body.

    • When using this product avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.

    • Stop use and ask a doctor if condition worsens or does not improve after regular use of this product as directed.

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

    • For best results, use at least twice a week or as directed by a doctor.
    • Wet hair thoroughly.
    • Massage shampoo into your scalp.
    • Lather, leaving on your hair and scalp for a few minutes.
    • Rinse and repeat.
  • Other information

    Store at room temperature.

  • Inactive ingredients

    Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Sodium Chloride, Polyquaternium-22, Sodium Citrate, Hexylene Glycol, Sodium Lauroyl Sarcosinate, Fragrance, Linoleamidopropyl PG-Dimonium Chloride Phosphate, Citric Acid, Sodium Hydroxide

  • Questions?

    Call 800-256-4247 or 215-273-8755 (collec t) or visit www.neutrogena.com

  • SPL UNCLASSIFIED SECTION

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

  • PRINCIPAL DISPLAY PANEL - 354 mL Bottle Carton

    NEUTROGENA

    Scalp Therapy TM

    Anti-Dandruff

    MEDICATED

    DAILY CONTROL

    1.8% SALICYLIC ACID

    SHAMPOO

    Neutrogena®

    DERMATOLOGIST RECOMMENDED BRAND

    12 FL OZ (354 mL)

    Ntg001

  • INGREDIENTS AND APPEARANCE
    NEUTROGENA SCALP THERAPY ANTI-DANDRUFF DAILY CONTROL 
    salicylic acid shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0722
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID18 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    LINOLEAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: 5Q87K461JO)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0722-1354 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/06/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03212/06/2021
    Labeler - Kenvue Brands LLC (118772437)
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