Label: KIEHLS SINCE 1851 BLUE HERBAL ACNE CLEANSER TREATMENT WITH FRANKINCENSE AND GINGER ROOT- salicylic acid lotion

  • NDC Code(s): 49967-086-01, 49967-086-02, 49967-086-03, 49967-086-04
  • 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

  • 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

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

    water, coco-glucoside, propylene glycol, ammonium polyacryloyldimethyl taurate, glycerin, coco-betaine, sodium cocoyl isethionate, sodium methyl cocoyl taurate, dipropylene glycol, sodium chloride, butylene glycol, phenoxyethanol, hydrogenated coconut acid, capryloyl salicylic acid, coconut acid, t-butyl alcohol, sodium pca, camphor, menthol, boswellia serrata extract, sodium isethionate, hamamelis virginiana (witch hazel) water, peumus boldus leaf extract, disodium EDTA, alcohol, zingiber officinale (ginger) root extract, sanguisorba officinalis root extract, cinnamomum cassia bark extract, xanthan gum, laminaria saccharina extract, zinc sulfate, pyridoxine HCL, sodium hydroxide, citric acid

  • Questions or comments?

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  • PRINCIPAL DISPLAY PANEL

    image of a label

    image of a label
  • INGREDIENTS AND APPEARANCE
    KIEHLS SINCE 1851 BLUE HERBAL ACNE CLEANSER TREATMENT WITH FRANKINCENSE AND GINGER ROOT 
    salicylic acid lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-086
    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 GLUCOSIDE (UNII: ICS790225B)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (55000 MPA.S) (UNII: F01RIY4371)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    COCO-BETAINE (UNII: 03DH2IZ3FY)  
    SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)  
    SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM)  
    CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4)  
    COCONUT ACID (UNII: 40U37V505D)  
    TERT-BUTYL ALCOHOL (UNII: MD83SFE959)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    MENTHOL (UNII: L7T10EIP3A)  
    INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
    SODIUM ISETHIONATE (UNII: 3R36J71C17)  
    HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V)  
    PEUMUS BOLDUS LEAF (UNII: Q4EWM09M3O)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ALCOHOL (UNII: 3K9958V90M)  
    GINGER (UNII: C5529G5JPQ)  
    SANGUISORBA OFFICINALIS ROOT (UNII: 4NYV2HT01X)  
    CHINESE CINNAMON (UNII: WS4CQ062KM)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    SACCHARINA LATISSIMA (UNII: 68CMP2MB55)  
    ZINC SULFATE (UNII: 89DS0H96TB)  
    PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-086-0175 mL in 1 TUBE; Type 0: Not a Combination Product04/26/2016
    2NDC:49967-086-02150 mL in 1 TUBE; Type 0: Not a Combination Product04/26/2016
    3NDC:49967-086-0330 mL in 1 TUBE; Type 0: Not a Combination Product04/26/2016
    4NDC:49967-086-043 mL in 1 PACKET; Type 0: Not a Combination Product04/26/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00604/26/2016
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    L'Oreal USA, Inc.185931458manufacture(49967-086) , pack(49967-086)
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