Label: ACNE WASH- salicylic acid liquid

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

Drug Label Information

Updated July 5, 2024

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  • Active Ingredient

    Active Ingredient Purpose

    Salicylic Acid 1% w/v

  • USE

    For the treatment of acne.

  • When using this product

    skin irritaion 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 medication at a time.

  • Directions

    Directions

    • Generously lather on body. For maximum lather, use a netted sponge or washcloth. Rinse thoroughly.
    • Avoid conttact with eyes. If contact occurs, flush thoroughly with water.
  • In active Ingredients

    Wate, Cocamidopropyl Betaine, Vegetable Glycerin, Sodium C14-C16 Olefin Sulfonate, PEG-120 Methyl Glucose Dioleate, Fragrance, Decyl Gliucoside, Salix Alba (Willow) Bark Extract, Camellia Sinensis Leaf Extract, Tetrasodium Glutamate Diacetate, Gluconolactone, Sodium Benzoate.

  • Distributed By: Target Corporation: Questions or Comments

    Distributed By:Target Corporation

    Minneapolis, MN 55403

    Questions or comments? Call 1-800-910-6874

    ORIGIN: USA WITH GLOBALLY SOURCED MATERIALS

  • Keep out of Reach of Children

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

  • Purpose

    Acne Medication

  • Store at Room Temperature

    Store at Room Temperature

  • WARNING

    For External Use Only

  • PRINCIPLE DISPLAY PANEL

    Principle display PanelCitrus Lime & Sunshine Scent Body Wash with 1% Salicylic Acid

    Contains green tea and willow bark extract

    Helps treat and reduce acne

    Lathers and foams well

    clarifies, nourishes and moissturizes

    Dermatologist Tested

    up &up Acne Control

    NDC 82442-801-01

    22 fl. oz (6565 mL)

  • INGREDIENTS AND APPEARANCE
    ACNE WASH 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82442-805
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID1 mg  in 100 mg
    Inactive Ingredients
    Ingredient NameStrength
    TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY) 1 mg  in 100 mg
    GLUCONOLACTONE (UNII: WQ29KQ9POT) 1 mg  in 100 mg
    FRAGRANCE 13576 (UNII: 5EM498GW35) 0.7 mg  in 100 mg
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) 0.05 mg  in 100 mg
    SODIUM BENZOATE (UNII: OJ245FE5EU) 1 mg  in 100 mg
    CAMELLIA SINENSIS SEED OIL (UNII: O5R6DK2M9K) 0.05 mg  in 100 mg
    WILLOW BARK (UNII: S883J9JDYX) 0.05 mg  in 100 mg
    WATER (UNII: 059QF0KO0R) 77.65 mg  in 100 mg
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V) 1 mg  in 100 mg
    GLYCERIN (UNII: PDC6A3C0OX) 4 mg  in 100 mg
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) 4 mg  in 100 mg
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y) 0.5 mg  in 100 mg
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82442-805-01650 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product09/30/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00609/30/2024
    Labeler - Target Corporation (006961700)
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