Label: ACNE BODY WASH- salicylic acid soap

  • NDC Code(s): 82575-110-30, 82575-110-40, 82575-110-50
  • Packager: Curology
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated August 7, 2024

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  • Active Ingredient

    Salicylic Acid 2%

  • Purpose

    Acne treatment

  • Uses

    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.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Dampen skin and massage a thin layer onto the entire affected area then rinse thoroughly.
    • 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.
  • Other Information

    Store at 20°-25°C (68°-77°F)

  • Inactive Ingredients

    Water, Sodium C14-16 Olefin Sulfonate, Glycerin, Cocamidopropyl Betaine, Cocamidopropyl Dimethylamine, Polygiyceryl-4 Caprate, Polyglyceryl-6 Caprylate, Hydroxypropyl Methylcellulose, Phenoxyethanol, Sodium Chloride, Zinc Pyrithione, Sodium Hydroxide, Polyquaternium-7, Ethylhexylglycerin, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Disodium EDTA, Sodium Benzoate

  • Questions?

    858-859-1188

  • Principal Display Panel – 100 mL Tube Label

    Curology

    Acne Body Wash

    2% Salicylic Acid Acne Treatment
    with clarifying tea tree oil

    DERMATOLOGIST
    FOUNDED•DEVELOPED•TESTED

    100 ml/3.4 fl oz

    Principal Display Panel – 100 mL Tube Label
  • INGREDIENTS AND APPEARANCE
    ACNE BODY WASH 
    salicylic acid soap
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82575-110
    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)  
    Cocamidopropyl Dimethylamine (UNII: L36BM7DG2T)  
    Hypromellose, Unspecified (UNII: 3NXW29V3WO)  
    Polyglyceryl-4 Caprate (UNII: 3N873UN885)  
    Polyglyceryl-6 Caprylate (UNII: DGV8R54VG7)  
    Phenoxyethanol (UNII: HIE492ZZ3T)  
    Pyrithione Zinc (UNII: R953O2RHZ5)  
    Polyquaternium-7 (70/30 Acrylamide/Dadmac; 1600000 MW) (UNII: 0L414VCS5Y)  
    Ethylhexylglycerin (UNII: 147D247K3P)  
    Sodium Hydroxide (UNII: 55X04QC32I)  
    Edetate Disodium Anhydrous (UNII: 8NLQ36F6MM)  
    Tea Tree Oil (UNII: VIF565UC2G)  
    Sodium Chloride (UNII: 451W47IQ8X)  
    Edetic Acid (UNII: 9G34HU7RV0)  
    Sodium Benzoate (UNII: OJ245FE5EU)  
    Formaldehyde/Sodium Naphthalenesulfonate Copolymer (3000 MW) (UNII: 90D834OZUI)  
    Xanthan Gum (UNII: TTV12P4NEE)  
    Magnesium Nitrate (UNII: 77CBG3UN78)  
    Methylchloroisothiazolinone (UNII: DEL7T5QRPN)  
    Magnesium Chloride (UNII: 02F3473H9O)  
    Methylisothiazolinone (UNII: 229D0E1QFA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82575-110-30267 mL in 1 TUBE; Type 0: Not a Combination Product12/01/2023
    2NDC:82575-110-40100 mL in 1 TUBE; Type 0: Not a Combination Product03/01/2024
    3NDC:82575-110-50200 mL in 1 TUBE; Type 0: Not a Combination Product03/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00612/01/2023
    Labeler - Curology (104103284)
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