Label: ALKMENE ANTI SPOT PAD- green tea liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated January 16, 2017

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  • PURPOSE

    Purpose -

    Provides especially gentle care for sensitive and blemished skin.

    It's special puricare pimple-fighting ingredient quickly and safely eliminates pimples and blemishes.

    The cooling effect of the Alkemene Blemish stick reduces redness and refreshes your complexion.

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENT

    Tea Tree Oil

  • DOSAGE & ADMINISTRATION

    Dab onto the affected area and let dry in the morning and evening, or several times a day if needed.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach

  • INACTIVE INGREDIENT

    LINALOOL
    ALLANTOIN
    GLYCERIN
    ASCORBYL PALMITATE
    TOCOPHEROL
    MANUKA OIL
    CARBOMER 934
    MAGNOLIA GRANDIFLORA BARK
    NIGELLA SATIVA SEED OIL
    ACRYLAMIDE
    HYDROGENATED PALM GLYCERIDES
    AMINO ACIDS
    POTASSIUM LAURATE
    LECITHIN, SUNFLOWER
    PHENOXYETHANOL
    BENZYL ALCOHOL
    LIMONENE
    SODIUM HYDROXIDE
    WATER
    ALCOHOL

  • INDICATIONS & USAGE

    Dab onto the affected area and let dry in the morning and evening or serveral times a day.

  • WARNINGS

    For external use.

  • PRINCIPAL DISPLAY PANEL

  • PRINCIPAL DISPLAY PANEL

    label 2label

  • INGREDIENTS AND APPEARANCE
    ALKMENE ANTI SPOT PAD 
    green tea liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71084-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TEA TREE OIL (UNII: VIF565UC2G) (TEA TREE OIL - UNII:VIF565UC2G) TEA TREE OIL48 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    ALLANTOIN (UNII: 344S277G0Z)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ASCORBYL PALMITATE (UNII: QN83US2B0N)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    MANUKA OIL (UNII: M6QU9ZUH2X)  
    CARBOMER 934 (UNII: Z135WT9208)  
    MAGNOLIA GRANDIFLORA BARK (UNII: J4XF5T6418)  
    NIGELLA SATIVA SEED OIL (UNII: CS4U38E731)  
    ACRYLAMIDE (UNII: 20R035KLCI)  
    HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)  
    POTASSIUM LAURATE (UNII: V4361R8N4Z)  
    AMINO ACIDS (UNII: 0O72R8RF8A)  
    LECITHIN, SUNFLOWER (UNII: 834K0WOS5G)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    .ALPHA.-(.ALPHA.-AMINOPROPYL)BENZYL ALCOHOL (UNII: S8TT5K3C8Y)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71084-001-0115 g in 1 BOTTLE; Type 0: Not a Combination Product01/16/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/16/2017
    Labeler - Mann & Schroeder GmbH (320623663)
    Establishment
    NameAddressID/FEIBusiness Operations
    Mann & Schroeder GmbH320623663manufacture(71084-001)
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