Label: FOAMING CLEANSER- salicylic acid liquid

  • NDC Code(s): 62742-4239-1, 62742-4239-2
  • Packager: Allure Labs
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 7, 2023

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  • ACTIVE INGREDIENT

    Active Ingredient:

    Salicylic Acid 2%

  • PURPOSE

    Purpose: Acne Treatment

  • INDICATIONS & USAGE

    Uses: For the treatment of acne

    Gently cleanses and maintains optimal moisture balance.

    For all skin types

  • WARNINGS

    Warning: For external use only

  • DO NOT USE

    If excessive dryness or peeling occurs

  • WHEN USING

    Avoid eye area

  • STOP USE

    If excessive dryness or peeling occurs

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • DOSAGE & ADMINISTRATION

    Direction:

    Use daily. Thoroughly lather foam over wet skin, rinse well and pat dry. Avoid eye area. If excessive dryness or peeling occurs, reduce application to every other day.

  • OTHER SAFETY INFORMATION

    Using other topical acne medication at the same time or immediately following use of this product may increase dryness or irritation of the skin.

    If this occurs, only one medication should be used unless directed by a doctor.

  • INACTIVE INGREDIENT

    Inactive Ingredient:

    Water (Aqua), Alkyl (C10-16) Ether Sulfate Sodium Salt, Cocamidopropyl Betaine, Butylene Glycol, Hydrolyzed Wheat Protein, Alcohol (C12-15 Ln. saturated), Ethoxylate, Hydrolyzed Wheat Starch, Caprylyl Glycol, Phenoxyethanol, Aloe Barbadensis Leaf Extract, Rosmarinus Officinalis ( Rosemary) Leaf Extract, Sodium Hydroxide, Ethylhexyl Glycerin, Hexylene Glycol, Sodium Chloride, Lavandula Angustifolia ( Lavender) Leaf Oil O.E., Glycerin.

  • PRINCIPAL DISPLAY PANEL

    Foaming Cleanser

  • INGREDIENTS AND APPEARANCE
    FOAMING CLEANSER 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62742-4239
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    C12-15 ALCOHOLS (UNII: 2C8M6XLB5C)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    1-ETHOXYUNDECANE (UNII: R428J6A8Q2)  
    WATER (UNII: 059QF0KO0R)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ROSEMARY (UNII: IJ67X351P9)  
    (C10-C16)ALKYLDIMETHYLAMINE OXIDE (UNII: LF6BKC321J)  
    STARCH, WHEAT (UNII: 79QS2MG2LP)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA LEAF (UNII: XY6Z280JTM)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62742-4239-150 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/07/2023
    2NDC:62742-4239-2125 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product12/07/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00612/07/2023
    Labeler - Allure Labs (926831603)
    Registrant - Allure Labs (926831603)
    Establishment
    NameAddressID/FEIBusiness Operations
    Allure Labs926831603manufacture(62742-4239)
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