KIEHLS SINCE 1851 BLUE HERBAL SPOT TREATMENT ACNE (SALICYLIC ACID) LOTION [L'OREAL USA PRODUCTS INC]

KIEHLS SINCE 1851 BLUE HERBAL SPOT TREATMENT ACNE (SALICYLIC ACID) LOTION [L'OREAL USA PRODUCTS INC]
PDF | XML

NDC 49967-615-01, 49967-615-02
Set ID 344bedc1-5228-4543-898e-895cac0bc336
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 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, alcohol denat., glycerin, glycolic acid, triethanolamine, ammonium polyacryloyldimethyl taurate, acrylates/C10-30 alkyl acrylate crosspolymer, pentylene glycol, butylene glycol, zinc gluconate, propylelne glycol, dipropylene glycol, camphor, menthol, aloe barbadensis leaf juice, boswellia serrata extract, laminaria saccharina extract, hammamelis viginiana (witch hazel) leaf extract, potarium officinale root exract, zingiber officinale (ginger) root extract, cimmamoum casaia bark extract

  • PRINCIPAL DISPLAY PANEL

    image of a label

  • INGREDIENTS AND APPEARANCE
    KIEHLS SINCE 1851 BLUE HERBAL SPOT TREATMENT ACNE 
    salicylic acid lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-615
    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)  
    ALCOHOL (UNII: 3K9958V90M)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCOLIC ACID (UNII: 0WT12SX38S)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    CAMPHOR (NATURAL) (UNII: N20HL7Q941)  
    MENTHOL (UNII: L7T10EIP3A)  
    WITCH HAZEL (UNII: 101I4J0U34)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-615-011 in 1 CARTON02/03/2014
    115 mL in 1 TUBE; Type 0: Not a Combination Product
    2NDC:49967-615-021.5 mL in 1 PACKET; Type 0: Not a Combination Product02/03/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333D02/03/2014
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    L'Oreal USA, Inc.185931458manufacture(49967-615)

Related Drugs