Label: ACNE WASH KISSABLE- salicylic acid gel

  • NDC Code(s): 50157-012-20, 50157-012-23
  • Packager: BRANDS INTERNATIONAL
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 26, 2024

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  • ACTIVE INGREDIENT

    Active Ingredient                     Purpose

    Salicylic Acid 2% ............Acne Treatment

  • PURPOSE

    for the treatment of Acne

  • 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.

  • INDICATIONS & USAGE

    For treatment of acne

  • DOSAGE & ADMINISTRATION

    Clean twice a day

    Wet face, apply to hands add water and work into a lather

    Massage fae gently

    Rinse thoroughly

  • WARNINGS

    Warning: for external use only.

    Ask a doctor or pharmacist before use if you are using other topical acne medications at the same time or immediately following use of this product. This may increase dryness or irritation of the skin. If this occurs, only one medication should be used unless directed by a doctor.

    When using this product avoid contact with eyes.  If contact occurs, flush thoroughly with water.

  • OTHER SAFETY INFORMATION

    Store at room temparture

  • INACTIVE INGREDIENT

    Inactive Ingredients:water, cocamidopropyl betaine, propylene glycol, sodium chloride, fragrance, Tetra sodium EDTA, aloe barbadensis leaf extract, methylchloroisothiazolinone, methylisothiazoline,

  • PRINCIPAL DISPLAY PANEL

    1

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  • INGREDIENTS AND APPEARANCE
    ACNE WASH  KISSABLE
    salicylic acid gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50157-012
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50157-012-20206 mL in 1 BOTTLE; Type 0: Not a Combination Product02/27/2023
    2NDC:50157-012-23236 mL in 1 BOTTLE; Type 0: Not a Combination Product02/27/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)02/27/2023
    Labeler - BRANDS INTERNATIONAL (243748238)
    Establishment
    NameAddressID/FEIBusiness Operations
    Brands International243748238manufacture(50157-012)
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