Label: U-MAX WRINKLE SERUM- adenosine liquid

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated June 4, 2012

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  • ACTIVE INGREDIENT

    active ingredient: adenosine
  • INACTIVE INGREDIENT

    inactive ingredient:  water, glycerin, disodium EDTA, carbomer, houttuynia cordata extract, xanthium strumarium fruit extract, angelica gigas root extract, glycyrrhiza glabra root extract, hydrolyzed soybean extract, artemisia vulgaris extract, actinidia chinensis fruit extract, musa sapientum fruit extract, aloe barbadensis leaf extract, perfurm, portulaca oleracea extract, salcornia herbacea extract, laminaria japonica extract, taraxacum officinale leaf extract, citrus paradisi seed oil, cellulose gum, betaine, peg-60 hydrogenated castor oil, triethanolamine, alcohol, methylparaben, cyclopentasioxane/dimethicone, cyclomethicone
  • PURPOSE

    skin protectant (anti-wrinkle)
  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children
  • INDICATIONS & USAGE

    - apply only for skin
    - apply 2 or 3 times a day with 5~6ml
    - massage with your finger over 2 min and let them dry


  • WARNINGS

    - keep out of eyes, ears and mouth
    - if contact occurs, rinse away with plenty of cold water
  • DOSAGE & ADMINISTRATION

    - for external use only
  • PRINCIPAL DISPLAY PANEL

    package label
  • INGREDIENTS AND APPEARANCE
    U-MAX WRINKLE SERUM 
    adenosine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50795-1001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE0.04 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22)  
    XANTHIUM STRUMARIUM FRUIT (UNII: TN770YC17C)  
    SOLANUM LYCOPERSICUM (UNII: 0243Q4990L)  
    ANGELICA GIGAS ROOT (UNII: 32766B2FHX)  
    GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)  
    ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S)  
    KIWI FRUIT (UNII: 71ES77LGJC)  
    BANANA (UNII: 4AJZ4765R9)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PURSLANE (UNII: M6S840WXG5)  
    SALICORNIA EUROPAEA (UNII: 6ADL50JAKW)  
    LAMINARIA JAPONICA (UNII: WE98HW412B)  
    TARAXACUM OFFICINALE (UNII: 39981FM375)  
    CITRUS PARADISI SEED (UNII: 12F08874Y7)  
    BETAINE (UNII: 3SCV180C9W)  
    POLYOXYL 60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)  
    ALCOHOL (UNII: 3K9958V90M)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    CYCLOMETHICONE (UNII: NMQ347994Z)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50795-1001-150 mL in 1 BOTTLE, WITH APPLICATOR
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/04/2012
    Labeler - VS Shinbi Co., Ltd. (557817055)
    Registrant - VS Shinbi Co., Ltd. (557817055)
    Establishment
    NameAddressID/FEIBusiness Operations
    VS Shinbi Co., Ltd.557817055manufacture