Label: VIRGIN GRACE HYALU PLUS SERUM- niacinamide, adenosine liquid

  • 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 September 17, 2019

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  • ACTIVE INGREDIENT

    Active Ingredient: Niacinamide 2.00%, Adenosine 0.04%

  • INACTIVE INGREDIENT

    Inactive Ingredients:

    Water, Glycerin, Butylene Glycol, 1,2-Hexanediol, Betaine, Sodium Hyaluronate, Hyaluronic Acid, Portulaca Oleracea Extract, Allantoin, Dipotassium Glycyrrhizate, Polyglyceryl-10 Laurate, Polyglyceryl-4 Laurate, Caprylyl/Capryl Glucoside, Copper Tripeptide-1, rh-Oligopeptide-1, Arginine, Disodium EDTA

  • PURPOSE

    Purpose: Skin Brightening, Anti wrinkle

  • WARNINGS

    Warnings:

    Keep out of reach of children.
    For external use only.
    Store away from direct sunlight.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • Uses

    Uses:
    Helps brighten skin tone.
    Helps improve wrinkle problem.

  • Directions

    Directions:

    After cleaning and toning face, apply Hyalu Plus by massaging into skin

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    VIRGIN GRACE HYALU PLUS SERUM 
    niacinamide, adenosine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73340-020
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide0.60 g  in 30 mL
    Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine0.01 g  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Glycerin (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73340-020-021 in 1 CARTON08/01/2019
    1NDC:73340-020-0130 mL in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other08/01/2019
    Labeler - Thanks & Vision Co., Ltd. (688398698)
    Registrant - Thanks & Vision Co., Ltd. (688398698)
    Establishment
    NameAddressID/FEIBusiness Operations
    BRCOS CO.,Ltd694769174manufacture(73340-020)