Label: LEBODY LAB RENEWAL DUAL EFFECT IDEBENONE SERUM- niacinamide, adenosine liquid

  • NDC Code(s): 71080-0008-1, 71080-0008-2
  • Packager: GTG Wellness Co., Ltd.
  • 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 February 24, 2023

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENTS

    Niacinamide 2%

    Adenosine 0.04%

  • INACTIVE INGREDIENTS

    Water, Butylene Glycol, Glycereth-26, Salicornia Herbacea Extract, Phragmites Communis Extract, Dipropylene Glycol, Ammonium Acryloyldimethyltaurate/VP Copolymer, Hydroxyacetophenone, Glycerin, Cellulose Gum, PEG-40 Hydrogenated Castor Oil, Caprylyl Glycol, Xanthan Gum, 1,2-Hexanediol, Hydrogenated Lecithin, Caprylic/Capric Triglyceride, Disodium EDTA, Panthenol, Hydroxydecyl Ubiquinone, Glycine Soja (Soybean) Sterols, Sodium Hyaluronate, Dipotassium Glycyrrhizate, Honey Extract, Beta-Glucan

  • PURPOSE

    Skin Brightening

    Anti wrinkle

  • Cautions

    1. In case of using cosmetics or after use, please consult a specialist if there is any abnormal symptom or side effect such as red spot, swelling or itching in direct sunlight.
    2. Do not use on wounded areas.
    3. Precautions for storage and handling
    a) Keep out of reach of children.
    b) Avoid direct sunlight.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • Uses

    ■ It makes improvement in skin tone evenness and level of brightness.

  • Directions

    ■ Apply the LEBODY LAB RENEWAL DUAL EFFECT SERUM to the back of your hand with the included applicator, then apply it to the area you want to use and rub lightly.

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    LEBODY LAB RENEWAL DUAL EFFECT IDEBENONE SERUM 
    niacinamide, adenosine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71080-0008
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide0.6 g  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Propanediol (UNII: 5965N8W85T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71080-0008-21 in 1 CARTON03/01/2019
    1NDC:71080-0008-130 mL in 1 CONTAINER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other03/01/2019
    Labeler - GTG Wellness Co., Ltd. (689458057)
    Registrant - GTG Wellness Co., Ltd. (689458057)
    Establishment
    NameAddressID/FEIBusiness Operations
    YUYU LnP Inc694752447manufacture(71080-0008)