Label: ULTRA V IDEBENONE NUTRITIONAL- niacinamide, adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 71975-030-01, 71975-030-02 - Packager: Ultra V Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated April 1, 2020
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients: Water, Glycerin, Cyclopentasiloxane, Dimethicone, Methylpropanediol, Centella Asiatica Extract, Cyclohexasiloxane, Alcohol , PEG/PPG-19/19 Dimethicone, Beta-Glucan , Biosaccharide Gum-1 , Piper Methysticum Leaf/Root/Stem Extract , Helianthus Annuus (Sunflower) Seed Oil , Dimethicone/Vinyl Dimethicone Crosspolymer , Butylene Glycol , Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Phenoxyethanol, Chlorphenesin, Caprylic/Capric Triglyceride , Phellinus Linteus Extract , Hydrogenated Lecithin , Glycine Soja (Soybean) Oil , Betaine , Acetyl Hexapeptide-8, rh-Oligopeptide-1, Copper Tripeptide-1 , Palmitoyl Tetrapeptide-7, Palmitoyl Tripeptide-1, PEG-40 Castor Oil , Sodium Metabisulfite, 1,2-Hexanediol , Glyceryl Acrylate/Acrylic Acid Copolymer, Glycine Soja (Soybean) Sterols , Disodium EDTA, Hydroxydecyl Ubiquinone , Propylene Glycol, Bixa Orellana Seed Oil , Sodium Hyaluronate, Tocopherol
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Uses
- Directions
- QUESTIONS
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ULTRA V IDEBENONE NUTRITIONAL
niacinamide, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71975-030 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:71975-030-02 1 in 1 CARTON 01/02/2018 1 NDC:71975-030-01 50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/02/2018 Labeler - Ultra V Co., Ltd (689004748) Registrant - Ultra V Co., Ltd (689004748) Establishment Name Address ID/FEI Business Operations NEW & NEW CO.,LTD. 557821160 manufacture(71975-030)