Label: DE MEDICOTEM ILLUMINATING WHITE CELL AMPOULE- niacinamide 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 January 30, 2019

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  • ACTIVE INGREDIENT

    Active ingredients: Niacinamide 2.2%

  • INACTIVE INGREDIENT

    Inactive ingredients:
    Water, Dipropylene Glycol, Glycereth-26, Human Stem Cell Conditioned Media, Glycerin, Butylene Glycol, 1,2-HEXANEDIOL, C12-13 Pareth-9, Synthetic Fluorphlogopite, Titanium Dioxide(CI77891), TinOxide, Camellia sinensis Callus Culture extracts, Bambusa Vulgaris Callus Culture Extract, Hydroxyethylacrylate/ Sodium Acryloyldimethyltaurate Copolymer, Butyrospermum Parkii(Shea Butter), Xanthan Gum, Betaine, Ferulic Acid, Pentylene Glycol, Beta-Glucan, Sclerotium gum, Fullerenes, Astaxanthin, Polyglyceryl-10 DIIsostearate, Caprylic/Capric Triglyceride, Sodium Hyaluronate, Hydrogenated Lecithin, Pvp

  • PURPOSE

    Purpose: Skin Brightening

  • WARNINGS

    Warnings:
    For external use only
    Avoid contact with eyes.
    Discontinue use if signs of irritation or rashes appear.
    Do not use on the wounded areas.
    Keep out of reach of children.
    Keep away from direct sunlight

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • Uses

    Uses:
    ■ Shines skin softly.
    ■ Corrects skin tone.
    ■ Protects the skin barrier and skin cell
    ■ Helps skin recovery
    ■ Calms down the worn-out skin
    ■ Maintain clear and bright skin

  • Directions

    Directions:
    ■ Every morning and night, after using a toner, apply it in a bottle(5ml) evenly over the skin three to four times and make it absorb. Recommended for use within two weeks of release.

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    DE MEDICOTEM ILLUMINATING WHITE CELL AMPOULE 
    niacinamide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72799-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE0.11 g  in 5 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Dipropylene Glycol (UNII: E107L85C40)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72799-010-0210 in 1 CARTON12/01/2018
    1NDC:72799-010-015 mL in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/01/2018
    Labeler - BELLANEZ (694798857)
    Registrant - BELLANEZ (694798857)
    Establishment
    NameAddressID/FEIBusiness Operations
    Nature Intro Co., Ltd.688282814manufacture(72799-010)