KIEHLS SINCE 1851 DERMATOLOGIST SOLUTIONS ACNE BLEMISH CONTROL DAILY SKIN CLEARING TREATMENT (SALICYLIC ACID) LOTION [L'OREAL USA PRODUCTS INC]

KIEHLS SINCE 1851 DERMATOLOGIST SOLUTIONS ACNE BLEMISH CONTROL DAILY SKIN CLEARING TREATMENT (SALICYLIC ACID) LOTION [L'OREAL USA PRODUCTS INC]
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NDC 49967-495-01, 49967-495-02
Set ID cdc9bc9c-2279-4cae-820d-f0b58848b8df
Category HUMAN OTC DRUG LABEL
Packager L'Oreal USA Products Inc
Generic Name
Product Class
Product Number
Application Number PART333D
  • Active ingredient

    Salicylic acid 1.5%

  • Purpose

    Acne treatment

  • Use

    for the treatment of acne

  • 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, DI-C12-13 alkyl malate, cyclohexasiloxane, propylene glycol, aluminum starch octenylsuccinate, PEG-100 stearate, glyceryl stearate, cetyl alcohol, sodium hydroxide, acrylates/C10-30 alkyl acrylate crosspolymer, capryloyl salicylic acid, xanthan gum, zinc PCA, iodopropynyl butylcarbamate, octadecenedioic acid

  • Questions or comments?

    Call toll free 1-800-946-4453

  • PRINCIPAL DISPLAY PANEL

    image of a label

  • INGREDIENTS AND APPEARANCE
    KIEHLS SINCE 1851 DERMATOLOGIST SOLUTIONS ACNE BLEMISH CONTROL DAILY SKIN CLEARING TREATMENT 
    salicylic acid lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-495
    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)  
    DI-C12-13 ALKYL MALATE (UNII: RRL7C51WPD)  
    CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    ZINC PIDOLATE (UNII: C32PQ86DH4)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    OCTADECENEDIOIC ACID (UNII: 565ZMT5QRG)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-495-011 in 1 CARTON11/01/2008
    130 mL in 1 TUBE; Type 0: Not a Combination Product
    2NDC:49967-495-025 mL in 1 PACKET; Type 0: Not a Combination Product11/01/2008
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D11/01/2008
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    L'Oreal USA, Inc.185931458manufacture(49967-495)

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