LEBODY LAB RENEWAL DUAL EFFECT IDEBENONE SERUM- niacinamide, adenosine liquid 
GTG Wellness Co., Ltd.

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.

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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

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)

Revised: 2/2023
Document Id: ee29d0ad-5047-49af-b2b9-4a523671ac22
Set id: 93e4b82b-63da-465e-b66d-e825aaf7e747
Version: 2
Effective Time: 20230224
 
GTG Wellness Co., Ltd.