Label: CLARIFYING TONER- 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 - 1%

  • PURPOSE

    Purpose: Acne Treatment

  • INDICATIONS & USAGE

    Uses:

    • For the treatment of acne.
    • Eliminates pore clogging impurities.
    • 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 excessive irritation occurs reduce application to once a day.
  • DOSAGE & ADMINISTRATION

    Directions:

    • Cleanse the skin thoroughly before applying medication.
    • Avoid eye area.
    • If excessive irritation, drying or peeling occurs, reduce application to once a day.
  • INACTIVE INGREDIENT

    Water (Aqua), SD Alcohol 40-B (Alcohol Denat.), Hamamelis Virginiana (Witch Hazel)  Water, Glycerine, Polysorbate 20, Symphytum Officinale (Comfrey)  Extract, Plantago Ovata (Indian Plantin) Seed Extract, Sodium PCA, Hydrolyzed Wheat Protein, Hydrolyzed Wheat Starch, Phenoxyethanol, Caprylyl Glycol, Ethylhexyl Glycerin, Rosmarinus Officinalis (Rosemary) Leaf Extract, Chamomilla Recutita (Chamomile) Flower Extract, Hexylene Glycol, Allantoin, Dipotassium Glycyrrhizate.

  • PRINCIPAL DISPLAY PANEL

    Advanced Skin Care

    Los Angeles, California 90025

    877-20-CLEAR

    clearogen.com

    made in USA

    image description

  • INGREDIENTS AND APPEARANCE
    CLARIFYING TONER 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62742-4070
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    COMFREY ROOT (UNII: M9VVZ08EKQ)  
    PLANTAGO OVATA SEED (UNII: UD50RBY30F)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    ROSEMARY (UNII: IJ67X351P9)  
    CHAMOMILE (UNII: FGL3685T2X)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    ALLANTOIN (UNII: 344S277G0Z)  
    GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62742-4070-1120 mL in 1 BOTTLE, PLASTIC
    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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