Label: W.SKIN WHITE GLUTATHIONE TONE UP- niacinamide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 74997-0012-1 - Packager: J&J COMPANY
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated May 7, 2021
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Onsen-Sui, Water, Butylene Glycol, Glycerin, Propylene Glycol Dicaprylate, Titanium Dioxide, Cyclopentasiloxane, Sodium Hyaluronate, Pentaerythrityl Tetraethylhexanoate, Niacinamide, PEG-10 Dimethicone, Dimethicone, Cyclohexasiloxane, Phenyl Trimethicone, 1,2-Hexanediol, Caprylyl Glycol, Ammonium Acryloyldimethyltaurate/VP Copolymer, Sodium Acrylate/Sodium AcryloyldimethylTaurate Copolymer, Glutathione, Persea Gratissima (Avovado) Oil, Allantoin, Isohexadecane, Thuja Orientalis Leaf Extract, Zanthoxylum Schinifolium Leaf Extract, Polygonum Cuspidatum Root Extract, Aloe Barbadensis Leaf Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Centella Asiatica Extract, ScutellariaBaicalensis Root Extract, Camellia Sinensis Leaf Extract, ChamomilaRecutita (Matricaria) Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Simmondsia Chinensis (Jojoba) Seed Oil, Ethylhexylglycerin, Adenosine, Dipotassium Glycyrrhizate, Polysorbate 80, Pentylene Glycol, Aspalathus Linearis Extract, Commiphora Myrrha Resin Extract, Perilla Frutescens Leaf Extract, Yucca Schidigera Root Extract
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
W.SKIN WHITE GLUTATHIONE TONE UP
niacinamide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74997-0012 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 2 g in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74997-0012-1 60 mL in 1 TUBE; Type 0: Not a Combination Product 05/08/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/08/2021 Labeler - J&J COMPANY (688995236) Registrant - J&J COMPANY (688995236) Establishment Name Address ID/FEI Business Operations J&J COMPANY 688995236 manufacture(74997-0012) , label(74997-0012) , pack(74997-0012)