Label: LEBODY FACE RENEWAL- glycerin gel

  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated December 26, 2017

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  • 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

    Image of carton

  • INGREDIENTS AND APPEARANCE
    LEBODY FACE RENEWAL 
    glycerin gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71080-0004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Glycerin (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) Glycerin15.0 g  in 150 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    1,2-Hexanediol (UNII: TR046Y3K1G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71080-0004-21 in 1 PACKAGE12/01/2017
    1NDC:71080-0004-1150 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other12/01/2017
    Labeler - GTG Wellness Co., Ltd. (689458057)
    Registrant - GTG Wellness Co., Ltd. (689458057)
    Establishment
    NameAddressID/FEIBusiness Operations
    Hansol Bio Co.,Ltd694046931manufacture(71080-0004)
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