Label: WF FACE FITNESS BTX COLLAGEN SOOTHING- niacinamide, adenosine gel
-
Contains inactivated NDC Code(s)
NDC Code(s): 71080-0014-1, 71080-0014-2 - Packager: GTG Wellness Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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 March 24, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Inactive ingredients:
Water, Glycerin, PEG-8, 1,2-Hexanediol, Butylene Glycol, Propanediol, Erythritol, Trehalose, Bacillus Ferment, Portulaca Oleracea Extract, Centella Asiatica Leaf Water, 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, Acetyl Hexapeptide-8, Copper Tripeptide-1, Palmitoyl Pentapeptide-4, rh-Oligopeptide-1, Ammonium Acryloyldimethyltaurate/VP Copolymer, Carbomer, Tromethamine, Allantoin, Hydrolyzed Collagen, Polyglyceryl-10 Laurate, Disodium EDTA, Dipotassium Glycyrrhizate, PEG-40 Hydrogenated Castor Oil, Caprylyl Glycol, PPG-26-Buteth-26, Ethylhexylglycerin, Fragrance
- PURPOSE
-
WARNINGS
Warnings:
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
-
INGREDIENTS AND APPEARANCE
WF FACE FITNESS BTX COLLAGEN SOOTHING
niacinamide, adenosine gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71080-0014 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 1.0 g in 50 mL Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.02 g in 50 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:71080-0014-2 1 in 1 CARTON 03/01/2020 1 NDC:71080-0014-1 50 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 03/01/2020 Labeler - GTG Wellness Co., Ltd. (689458057) Registrant - GTG Wellness Co., Ltd. (689458057) Establishment Name Address ID/FEI Business Operations Hansol Bio Co.,Ltd 694046931 manufacture(71080-0014)