ARMIYOU HYDROGEN TONER (ADENOSINE) LIQUID [ARMIYOU]

ARMIYOU HYDROGEN TONER (ADENOSINE) LIQUID [ARMIYOU]
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NDC 71878-010-01, 71878-010-02
Set ID 1bd32ac4-225b-4df1-839a-19689425d844
Category HUMAN OTC DRUG LABEL
Packager Armiyou
Generic Name
Product Class Adenosine Receptor Agonist
Product Number
Application Number
  • ACTIVE INGREDIENT

    Active ingredients: Adenosine 0.04%

  • INACTIVE INGREDIENT

    Inactive ingredients: Water, Butylene Glycol, Glycerin, Alcohol, PEG-60 Hydrogenated Castor Oil, Phenoxyethanol, Allantoin, Carbomer, Panthenol, Sodium Benzoate, Triethanolamine, Flavor, Centella Asiatica Extract, Ethylhexylglycerin, Polygonum Cuspidatum Root Extract, Tocopheryl Acetate, Scutellaria Baicalensis Root Extract, Polyquaternium-51, Camellia Sinensis Leaf Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Anthemis Nobilis Flower Extract, Sodium Hyaluronate, Pueraria Mirifica Root Extract

  • PURPOSE

    Purpose: Anti wrinkle

  • WARNINGS

    Warnings: For external use only Avoid contact with eyes. Discontinue use if signs of irritation or rashes appear. Replace the cap after use. Keep Out of Reach of Children. Avoid use in areas affected by wounds.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • Uses

    Uses: Helps prevent wrinkles

  • Directions

    Directions: After washing your face in the morning and at night, dispense 1-2 pumps onto a cotton pad, and apply to your skin in a gentle, wiping motion.

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    ARMIYOU HYDROGEN TONER 
    adenosine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71878-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine0.04 g  in 120 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Butylene Glycol (UNII: 3XUS85K0RA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71878-010-021 in 1 CARTON10/01/2017
    1NDC:71878-010-01120 mL in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/01/2017
    Labeler - Armiyou (694891814)
    Registrant - Armiyou (694891814)
    Establishment
    NameAddressID/FEIBusiness Operations
    Armiyou694891814manufacture(71878-010)

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