Label: FOAMING CLEANSER- salicylic acid liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated June 7, 2014

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  • ACTIVE INGREDIENT

    Active Ingredient:

    Salicylic Acid - 2%

  • PURPOSE

    Purpose: Acne Treatment

  • DOSAGE & ADMINISTRATION

    Uses:

    • For the treatment of acne
    • Gently cleanses and maintains optimal moisture balance
    • For all skin types
  • WARNINGS

    Warnings:

    • For external use only.
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children

  • WHEN USING

    • Using other topical acne medications 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.
  • INDICATIONS & USAGE

    Directions:

    • 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.
  • INACTIVE INGREDIENT

    Water (Aqua), Alkyl (C10-16) Ether Sulfate Sodium Salt, Cocamidopropyl Betaine, Butylene Glycol, Hydrolyzed Wheat Protein, Alcohols (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

    Advanced Skin & Hair

    Los Angeles, California 90025

    877-30-CLEAR

    clearogen.com

    Made In USA

    ImageFC42

  • INGREDIENTS AND APPEARANCE
    FOAMING CLEANSER 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62742-4071
    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)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)  
    C12-15 ALCOHOLS (UNII: 2C8M6XLB5C)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ROSEMARY (UNII: IJ67X351P9)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62742-4071-1125 mL in 1 BOTTLE, PUMP
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D06/07/2014
    Labeler - Allure Labs, Inc (926831603)
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