Label: ANTIBE BEAUSENNE SPECIAL AMPOULE- niacinamide, adenosine gel

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

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 August 22, 2016

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENT

    NIACINAMIDE, ADENOSINE

  • INACTIVE INGREDIENT

    PURIFIED WATER, BUTYLENE GLYCOL, METHYL GLUCETH-20, HYDROXYETHYL UREA, PEGㆍPPG(18:4) COPOLYMER, BIOSACCHARIDEGUM-1, BETA-GLUCAN, SODIUM HYALURONATE, HYDROLYZED EXTENSIN, HYDROLYZED COLLAGEN, HYDROLYZED ELASTIN, PROPOLIS EXTRACT, PERSIMMON EXTRACT, SODIUM POLYACRYLATE, DIMETHICONE, CYCLOPENTASILOXANE, TRIDECETH-16, PEGㆍPPG(18:18) DIMETHICONE, CAVIAR EXTRACT, RH OLIGOPEPTIDE-1, ALLANTOIN, PANTHENOL, ACRYLATE/C10-30ALKYL ACRYLATE CROSSPOLYMER, CARBOMER, LILIUM CANDIDUM BULB EXTRACT, ALOE VERA EXTRACT, CENTELLA EXTRACT, CHAMOMILE EXTRACT, LICORICE ROOT EXTRACT, GREEN TEA EXTRACT, JAPANESE KNOTWEED EXTRACT, ROSEMARY EXTRACT, GOLD EXTRACT, JAPANESE BEAUTYBERRY EXTRACT, BLUEBERRY EXTRACT, ACAI PALM EXTRACT, POMEGRANATE EXTRACT, FIG EXTRACT, MULBERRY LEAF EXTRACT, GINKGO LEAF EXTRACT, STEARYL ALCOHOL, STEARIC ACID, GLYCERYL STEARATE, HYDROGENATED LECITHIN, COTTON PLANT CELL EXTRACT, HOUTTUYNIA CORDATA EXTRACT, HOP MARJORAM EXTRACT, GREATER GALANGAL LEAF EXTRACT, MULBERRY ROOT EXTRACT, TETRAHEXYL DECYL ASCOBATE, TOCOPHERYL ACETATE, SQUALANE, GLYCERYL LINOLATE/GLYCERYLLINOLATE/GRLYCERYL ARACHIDONATE, SHIITAKE MYCELIUM EXTRACT, CERAMIDE NP, RETINYL PALMITATE, CYCLOPENTASILOXANE, CETYL ETHYL HEXANOATE, PEG-60 HYDROGENATED CASTOR OIL, TRIETHANOLAMINE, ETHYLTEXYL GLYCERIN, PHENOXYETHANOL, DISODIUM EDTA, YELLOW NO.4, YELLOW NO.5, FRAGRANCE

  • PURPOSE

    Reenergize your skin with rich E.G.F. and natural herbs, fortified with vitamin-rich caviar extract.

  • KEEP OUT OF REACH OF CHILDREN

    keep out or reach of the children

  • INDICATIONS & USAGE

    After cleansing, apply an appropriate amount of product on the face and neck area and gently pat for absorption. Use twice daily as the first step of your morning and night skin care regimen.

  • WARNINGS

    1. Do not use in the following cases(Eczema and scalp wounds)
    2.Side Effects
    1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
    3.General Precautions
    1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
    2)This product is for exeternal use only. Do not use for internal use
    4.Storage and handling precautions
    1)If possible, avoid direct sunlight and store in cool and area of low humidity
    2)In order to maintain the quality of the product and avoid misuse
    3)Avoid placing the product near fire and store out in reach of children

  • DOSAGE & ADMINISTRATION

    for external use only


  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    ANTIBE BEAUSENNE SPECIAL AMPOULE 
    niacinamide, adenosine gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70929-0002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE0.04 g  in 100 mL
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ALLANTOIN (UNII: 344S277G0Z)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70929-0002-24 in 1 BOX08/22/2016
    1NDC:70929-0002-150 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/01/2015
    Labeler - Modongee Co., Ltd. (688730710)
    Registrant - Modongee Co., Ltd. (688730710)
    Establishment
    NameAddressID/FEIBusiness Operations
    Modongee Co., Ltd.688730710manufacture(70929-0002)