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

  • NDC Code(s): 71080-0012-1, 71080-0012-2
  • Packager: GTG Wellness Co., Ltd.
  • 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 24, 2023

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • ACTIVE INGREDIENTS

    Niacinamide 2%

    Adenosine 0.04%

  • INACTIVE INGREDIENTS

    Water, Butylene Glycol, Dipropylene Glycol, Glycerin, 1,2-Hexanediol, Carbomer, Arginine, PEG-60 Hydrogenated Castor Oil, Ethylhexylglycerin, Thymus Vulgaris (Thyme) Extract, Origanum Vulgare Flower/Leaf/Stem Extract, Rosmarinus Officinalis (Rosemary) Extract, Lavandula Angustifolia (Lavender) Extract, Disodium EDTA, Gold, Xanthan Gum, Melaleuca Alternifolia (Tea Tree) Extract, Lavandula Angustifolia (Lavender) Oil, Cymbopogon Flexuosus Oil, Camellia Sinensis Leaf Extract, Sodium Hyaluronate

  • 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 BTX COLLAGEN 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 BTX COLLAGEN SERUM 
    niacinamide, adenosine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71080-0012
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide0.6 g  in 30 mL
    Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine0.012 g  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Glycerin (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71080-0012-21 in 1 CARTON03/01/2019
    1NDC:71080-0012-130 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(71080-0012)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!