OTC Medication Information: LEBODY FACE RENEWAL

LEBODY FACE RENEWAL- glycerin gel
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.

ACTIVE INGREDIENT

Active ingredients: Glycerin 10%

INACTIVE INGREDIENT

Inactive ingredients:

Water, 1,2-Hexanediol, Butylene Glycol, Portulaca Oleracea Extract, Hydrolyzed Collagen, Centella Asiatica Leaf Water, Dipotassium Glycyrrhizate, Erythritol, Trehalose, Allantoin, Bacillus Ferment, Ilex Paraguariensis Leaf Extract, Chenopodium Quinoa Seed Extract, Glutamic Acid, Glycine, Serine, Aspartic Acid, Leucine, Alanine, Lysine, Arginine, Tyrosine, Phenylalanine, Valine, Threonine, Proline, Isoleucine, Histidine, Methionine, Cysteine, Propanediol, Polyglyceryl-10 Laurate, Disodium EDTA, Ammonium Acryloyldimethyltaurate/VP Copolymer, Carbomer, Tromethamine, Fragrance

PURPOSE

Purpose: Skin moisturizing

WARNINGS

Warnings: 1) If there are abnormal symptoms such as red spots, swelling, itching or side effects when you use cosmetics or due to direct sunlight, consult with a specialist. 2) Do not use in wounded areas. 3) Precautions for storage and handling. 4) Keep out of reach for children. 5) Keep away from direct sunlight.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach for children.

Uses

Uses: It provides nutrition and moisture to your skin effectively.

Directions

Directions: Apply this solution to the area where you want to use LIFTING mode of LEBODY FACE after cleansing and drying the face.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LEBODY FACE RENEWAL glycerin gel

Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71080-0004 Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Glycerin (GLYCERIN) Glycerin 15.0 g in 150 mL

Inactive Ingredients Ingredient Name Strength Water 1,2-Hexanediol

Packaging # Item Code Package Description Multilevel Packaging 1 NDC:71080-0004-2 1 TUBE in 1 PACKAGE contains a TUBE (71080-0004-1) 1 NDC:71080-0004-1 150 mL in 1 TUBE This package is contained within the PACKAGE (71080-0004-2)

Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/01/2017

Labeler — GTG Wellness Co., Ltd. (689458057)

Registrant — GTG Wellness Co., Ltd. (689458057)

Establishment
Name	Address	ID/FEI	Operations
Hansol Bio Co.,Ltd		694046931	manufacture (71080-0004)

Revised: 12/2017 GTG Wellness Co., Ltd.