Label: APPLICELL ESSENTIAL TONER- adenosine liquid

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

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Drug Label Information

Updated November 25, 2016

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  • ACTIVE INGREDIENT

    Active Ingredient: Adenosine 0.04%

  • INACTIVE INGREDIENT

    Inactive Ingredients: Water, Alcohol, Sodium Hyaluronate, Portulaca Oleracea Extract, Hydrolyzed Keratin, Hydrolyzed Collagen, Hydrolyzed Elastin, Betaine, Trehalose, Citrus Paradisi (Grapefruit) Fruit Extract, Methyl Gluceth-20, Caprylhydroxamic Acid, Caprylyl Glycol, Human fibroblast Conditioned Media, PEG-40 Hydrogenated Castor Oil, Neofinetia Falcata Callus Culture Extract, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Xanthan Gum, Potassium Hydroxide, Phenoxyethanol, Fragrance

  • PURPOSE

    Purpose: Skin Protectant

  • WARNINGS

    Warnings: For external use only When using this product do not get into eyes, Stop use and ask a doctor if rash occurs Do not use on - deep puncture wounds - animal bites - serious burns Keep out of reach of children

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • INDICATIONS & USAGE

    Indications & usage: APPLICELL Essential Toner is the wrinkle functional toner that provides moisture, a silky feel and nourishment to the skin.

  • DOSAGE & ADMINISTRATION

    How to use: After cleansing, take proper amount and apply over the face along skin texture.

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    APPLICELL ESSENTIAL TONER 
    adenosine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71098-020
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine0.05 g  in 130 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Alcohol (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71098-020-021 in 1 CARTON10/10/2016
    1NDC:71098-020-01130 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/10/2016
    Labeler - Anc HnB Inc. (689031836)
    Registrant - Anc HnB Inc. (689031836)
    Establishment
    NameAddressID/FEIBusiness Operations
    Anc HnB Inc.689031836manufacture(71098-020)
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