Label: KIEHLS SINCE 1851 DERMATOLOGIST SOLUTIONS BREAKOUT CONTROL ACNE TREATMENT FACIAL- salicylic acid lotion

  • NDC Code(s): 49967-875-01, 49967-875-02, 49967-875-03, 49967-875-04, view more
    49967-875-05
  • 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 1.5%

  • Purpose

    Acne treatment

  • Uses

    • for the treatment of acne
    • helps prevent new acne blemishes
  • 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 increase to two or three times daily if needed or as directed by a doctor
    • if bothersome dryness or peeling occurs, reduce application to once a day or every other day
  • Inactive ingredients

    water, aloe barbadensis leaf juice, di-C12-13 alkyl malate, niacinamide, cyclohexasiloxane, propylene glycol, aluminum starch octenylsuccinate, PEG-100 stearate, glyceryl stearate, cetyl alcohol, acrylates/C10-30 alkyl acrylate crosspolymer, sodium hydroxide, capryloyl salicylic acid, xanthan gum, zinc PCA, zingiber officinale (ginger) root extract, stearyl alcohol, myristyl alcohol, citric acid, potassium sorbate, octadecenedioic acid, sodium benzoate, citral, BHT

  • 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 BREAKOUT CONTROL ACNE TREATMENT FACIAL 
    salicylic acid lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-875
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID15 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    MYRISTYL ALCOHOL (UNII: V42034O9PU)  
    OCTADECENEDIOIC ACID (UNII: 565ZMT5QRG)  
    CITRAL (UNII: T7EU0O9VPP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-875-011 in 1 CARTON11/01/201611/01/2016
    160 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:49967-875-025 mL in 1 PACKET; Type 0: Not a Combination Product11/01/2016
    3NDC:49967-875-031.5 mL in 1 PACKET; Type 0: Not a Combination Product11/01/2016
    4NDC:49967-875-045 mL in 1 TUBE; Type 0: Not a Combination Product11/01/2016
    5NDC:49967-875-051 in 1 CARTON11/01/2016
    560 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00611/01/2016
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    L'Oreal USA, Inc.185931458manufacture(49967-875) , pack(49967-875)
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