Label: CLARIFYING TONER- salicylic acid liquid

  • NDC Code(s): 62742-4240-1, 62742-4240-2
  • Packager: Allure Labs
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 8, 2023

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  • ACTIVE INGREDIENT

    Active Ingredient:

    Salicylic Acid 1%

  • 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:

    Cleanse the skin thoroughly before applying medication. Avoid eye area. If excessive dryness or peeling occurs, reduce application to once a 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), Alcohol Denat, Hamamelis Virginiana (Witch Hazel) Leaf Water, Ethoxydiglycol, Niacinamide, Glycerin, Polysorbate 20, 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

    Clarifying Toner

  • INGREDIENTS AND APPEARANCE
    CLARIFYING TONER 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62742-4240
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ROSEMARY (UNII: IJ67X351P9)  
    MATRICARIA RECUTITA FLOWERING TOP (UNII: 3VNC7T6Z02)  
    ALLANTOIN (UNII: 344S277G0Z)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    PLANTAGO OVATA SEED (UNII: UD50RBY30F)  
    DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
    STARCH, WHEAT (UNII: 79QS2MG2LP)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    HAMAMELIS VIRGINIANA LEAF WATER (UNII: 8FP93ED6H2)  
    ALCOHOL (UNII: 3K9958V90M)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    WATER (UNII: 059QF0KO0R)  
    HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)  
    GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62742-4240-1120 g in 1 BOTTLE; Type 0: Not a Combination Product12/08/2023
    2NDC:62742-4240-260 g in 1 BOTTLE; Type 0: Not a Combination Product12/08/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00612/08/2023
    Labeler - Allure Labs (926831603)
    Registrant - Allure Labs (926831603)
    Establishment
    NameAddressID/FEIBusiness Operations
    Allure Labs926831603manufacture(62742-4240)
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