Label: KIEHLS SINCE 1851 DERMATOLOGIST SOLUTIONS TRULY TARGETED ACNE CLEARING SOLUTION- salicylic acid liquid

  • NDC Code(s): 49967-055-01, 49967-055-02, 49967-055-03
  • Packager: L'Oreal USA Products Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 30, 2023

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  • Active ingredient


    Salicylic acid 2%

  • Purpose

    Acne treatment

  • Use

    • for the treatment of acne
    • helps clear up acne blemishes and allows skin to heal
  • Warnings

    For external use only

  • When using this product

    skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time. 

  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • clean the skin thoroughly before applying this product
    • cover the entire affected area with a thin layer one to three times daily
    • because excessive drying of the skin may occur, start with one application daily, then gradually ingrease to two or three times dialy if neded or as directed by a doctor
    • if bothersome dryness or peeling occurs, reduce application to once a day or every other dayl
  • Inactive ingredients

    water, gluconolactone, niacinamide, butylene glycol, glycolic acid, sodium hydroxide, glycerin, methyl gluceth-20, hydroxyethylcellulose, caprylyl glycol, dipotassium glycyrrhizate

  • Questions or comments?

    Call toll-free 1-800-946-4453

  • PRINCIPAL DISPLAY PANEL

    image of a carton

    image of a carton
  • INGREDIENTS AND APPEARANCE
    KIEHLS SINCE 1851 DERMATOLOGIST SOLUTIONS TRULY TARGETED ACNE CLEARING SOLUTION 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-055
    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)  
    GLUCONOLACTONE (UNII: WQ29KQ9POT)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYL GLUCETH-20 (UNII: J3QD0LD11P)  
    HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-055-011 in 1 CARTON06/01/2023
    115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    2NDC:49967-055-024 mL in 1 VIAL; Type 0: Not a Combination Product06/01/2023
    3NDC:49967-055-032 mL in 1 PACKET; Type 0: Not a Combination Product06/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00606/01/2023
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    L'Oreal USA, Inc.185931458manufacture(49967-055) , pack(49967-055)
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