Label: DO GOOD DEEP AQUA TREATMENT TONER- niacinamide, 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 February 22, 2018

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  • ACTIVE INGREDIENT

    Active ingredients: Niacinamide 2.0%, Adenosine 0.04%

  • INACTIVE INGREDIENT

    Inactive ingredients:

    Water, Butylene Glycol, Dipropylene Glycol, 1,2-Hexanediol, Glycerin, Propanediol, Diethoxyethyl Succinate, Glycereth-26, Chondrus Crispus Extract, PEG-60 Hydrogenated Castor Oil, Saccharum Officinarum (Sugarcane) Extract, Ethylhexylglycerin, Xanthan Gum, Sodium Hyaluronate, Pseudoalteromonas Ferment Extract, Sea Water, Caprylyl Glycol

  • PURPOSE

    Purpose: Skin Brightening, 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

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • Uses

    Uses:

    - Helps brighten skin

    - Helps Anti Wrinkle

  • Directions

    Directions:

    After cleansing, apply a suitable amount into hands or cotton pad and wipe gently over face.

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    DO GOOD DEEP AQUA TREATMENT TONER 
    niacinamide, adenosine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72058-050
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide3.00 g  in 150 mL
    Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine0.06 g  in 150 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Butylene Glycol (UNII: 3XUS85K0RA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72058-050-021 in 1 CARTON01/02/2018
    1NDC:72058-050-01150 mL in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/02/2018
    Labeler - WOOREE Colourone Co.,Ltd (694492496)
    Registrant - WOOREE Colourone Co.,Ltd (694492496)
    Establishment
    NameAddressID/FEIBusiness Operations
    Cosmax, Inc.689049693manufacture(72058-050)