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

KIEHLS SINCE 1851 BLUE HERBAL GEL CLEANSER ACNE TREATMENT (SALICYLIC ACID) LOTION [L'OREAL USA PRODUCTS INC]
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NDC 49967-617-01, 49967-617-02, 49967-617-03
Set ID effa0d12-65b5-48b7-a4eb-9177f58b2539
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

    • use twice daily
    • wet facem then work product into a lather
    • massage onto face, avoiding the eyes
    • rinse well
  • Inactive ingredients

    water, coco-glucoside, propylene glycol, sorbitol, sodium laureth sulfate, treithanolamine, sodium chloride, PEG-120 methyl glucose dioleate, menthol, methylparaben, imidazolidinyl urea, benzophenone-4, disodium EDTA, dipropylene glycol, camphor, zinc PCA, aloe barbadensis leaf juice, boswella serrata extract, laminaria saccharina extract, blue 1, poterium officinale root extract, zinber officinale (ginger) root extract, cinnamomum cassia bark extract, hammamelis virginiana (witch hazel) leaf extract

  • PRINCIPAL DISPLAY PANEL

    image of a label

  • INGREDIENTS AND APPEARANCE
    KIEHLS SINCE 1851 BLUE HERBAL GEL CLEANSER ACNE TREATMENT 
    salicylic acid lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-617
    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)  
    COCO-BETAINE (UNII: 03DH2IZ3FY)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SORBITOL (UNII: 506T60A25R)  
    SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)  
    MENTHOL (UNII: L7T10EIP3A)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    WITCH HAZEL (UNII: 101I4J0U34)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-617-01125 mL in 1 TUBE; Type 0: Not a Combination Product02/03/2014
    2NDC:49967-617-02200 mL in 1 TUBE; Type 0: Not a Combination Product02/03/2014
    3NDC:49967-617-03250 mL in 1 TUBE; 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(49967-617)

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