Label: ULTRA V IDEBENONE AMPOULE- niacinamide, adenosine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 71975-020-01, 71975-020-02 - 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:
Part 1: Water, Butylene Glycol , Glycerin , Caprylic/Capric Triglyceride , Hydrogenated Lecithin , PEG-40 Castor Oil , Glycine Soja (Soybean) Sterols , 1,2-Hexanediol , Hydroxydecyl Ubiquinone , Citrus Aurantium Bergamia (Bergamot) Fruit Oil, Tocopheryl Acetate
Part 2: Water, Galactomyces Ferment Filtrate , Butylene Glycol, Polyglutamic Acid, Tremella Fuciformis Sporocarp Extract , Glycerin, Panthenol, Ammonium Acryloyldimethyltaurate/VP Copolymer, Sodium Hyaluronate, Caprylyl Glycol, Acetyl Hexapeptide-8, rh-Oligopeptide-1, Palmitoyl tripeptide-1, Palmitoyl Tetrapeptide-7, Magnolia Officinalis Bark Extract, Caprylhydroxamic Acid, Cellulose Gum, Sodium Polyacrylate , Chondrus Crispus (Carrageenan) , PVM/MA Copolymer , Torreya Nucifera Extract , Cornus Kousa Extract , Rosa Multiflora Fruit Extract , Chloranthus Glaber Extract , Musa Basjoo Extract, Vaccinium Macrocarpon (Cranberry) Fruit Extract , Fragaria Chiloensis (Strawberry) Fruit Extract , Rubus Idaeus (Raspberry) Fruit Extract , Rubus Fruticosus (Blackberry) Fruit Extract , Vaccinium Angustifolium (Blueberry) Fruit Extract , Vaccinium Myrtillus Fruit Extract , Euterpe Oleracea Fruit Extract , Aronia Melanocarpa Fruit Extract
- 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 AMPOULE
niacinamide, adenosine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71975-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 0.12 g in 6 mL Adenosine (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) Adenosine 0.002 g in 6 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Butylene Glycol (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71975-020-02 4 in 1 CARTON 01/02/2018 1 NDC:71975-020-01 6 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 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(71975-020)
