Label: MEDI HYDRO DP B TOX AMPOULE- adenosine liquid

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

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Drug Label Information

Updated January 24, 2019

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  • INDICATIONS & USAGE

    Open the lid, press the lid to fill the dropper and apply evenly 3-4 drops to the desired parts, gently tap with the fingers to allow it to absorb

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • DOSAGE & ADMINISTRATION

    for external use only

  • WARNINGS

    Discontinue use of the product if any of the following symptoms occurred. Consult a dermatologist if the symptoms got worse.
    a) If redness, Swelling, Itchiness, Irritation occurred during using.
    b) If the above symptoms started to occur when exposed to direct sunlight.
    Do not use on skins with wounds, eczema or dermatitis.

    Storage instructions
    a) Always close the lid after finish using.
    b) Store in a safe place away and out of reach of children.
    c) Store in a place with not too high or low temperature, keep awayfrom direct sunlight exposure.

  • PURPOSE

    Ampoule that provides skin elasticity with active ingredients such as atelocollagen and 3D hyaluronic acid.

  • INACTIVE INGREDIENT

    water, butylene glycol, hyaluronic acid, etc.

  • ACTIVE INGREDIENT

    ADENOSINE

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    MEDI HYDRO DP B TOX AMPOULE 
    adenosine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70694-0010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE0.04 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70694-0010-130 mL in 1 BOTTLE; Type 0: Not a Combination Product01/24/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/24/2019
    Labeler - Inc MBG (688436167)
    Establishment
    NameAddressID/FEIBusiness Operations
    Inc MBG688436167manufacture(70694-0010)
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