Label: LEBODY LAB RENEWAL DUAL EFFECT PEPTIDE SERUM- niacinamide, adenosine liquid
- NDC Code(s): 71080-0009-1, 71080-0009-2
- Packager: GTG Wellness Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated February 24, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
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INACTIVE INGREDIENTS
Water, Dipropylene Glycol, Glycereth-26, Hydroxyacetophenone, Ammonium Acryloyldimethyltaurate/VP Copolymer, Xanthan Gum, Caprylyl Glycol, Propanediol, Polyglyceryl-10 Laurate, 1,2-Hexanediol, Disodium EDTA, Sodium Hyaluronate, Lactobacillus/Collagen Ferment Filtrate, Glyceryl Glucoside, Butylene Glycol, Hamamelis Virginiana (Witch Hazel) Extract, Dipotassium Glycyrrhizate, Glycerin, Borago Officinalis Extract, Corchorus Olitorius Leaf Extract, Ilex Paraguariensis Leaf Extract, Daucus Carota Sativa (Carrot) Root Extract, Palmitoyl Pentapeptide-4
- PURPOSE
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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
- Uses
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LEBODY LAB RENEWAL DUAL EFFECT PEPTIDE SERUM
niacinamide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71080-0009 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 0.6 g in 30 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71080-0009-2 1 in 1 CARTON 03/01/2019 1 NDC:71080-0009-1 30 mL in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/01/2019 Labeler - GTG Wellness Co., Ltd. (689458057) Registrant - GTG Wellness Co., Ltd. (689458057) Establishment Name Address ID/FEI Business Operations YUYU LnP Inc 694752447 manufacture(71080-0009)