Label: ULTRA V IDEBANONE- niacinamide, adenosine cream
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Contains inactivated NDC Code(s)
NDC Code(s): 71975-040-01, 71975-040-02 - 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, Dimethicone, Glycerin, Methylpropanediol, 1,2-Hexanediol , Macadamia Ternifolia Seed Oil, Persea Gratissima (Avocado) Oil, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer , Helianthus Annuus (Sunflower) Seed Oil , Isohexadecane, Betaine , Cyclopentasiloxane , Cetearyl Alcohol , Dimethicone/Vinyl Dimethicone Crosspolymer , Arginine, Carbomer , Polysorbate 80, Butylene Glycol , Glycine Soja (Soybean) Oil , Cetearyl Glucoside, Caprylic/Capric Triglyceride , Sorbitan Oleate , Phellinus Linteus Extract , Hydrogenated Lecithin, Lavandula Angustifolia (Lavender) Oil , Sodium Hyaluronate, PEG-40 Castor Oil, Disodium EDTA, Glycine Soja (Soybean) Sterols , Citrus Grandis (Grapefruit) Peel Oil, Biosaccharide Gum-1 , Beta-Glucan , Centella Asiatica Extract, Bixa Orellana Seed Oil, Acetyl Hexapeptide-8, rh-Oligopeptide-1, Piper Methysticum Leaf/Root/Stem Extract, Copper Tripeptide-1, Palmitoyl Tetrapeptide-7, Palmitoyl Tripeptide-1, Hydroxydecyl Ubiquinone, Cananga Odorata Flower Oil, Tocopherol, Chrysanthellum Indicum Extract, Rheum Palmatum Root/Stalk Extract, Asarum Sieboldi Root Extract, Larix Sibirica Wood Extract, Quercus Mongolia Leaf Extract, Persicaria Hydropiper Extract, Illicium Verum (Anise) Fruit Extract, Corydalis Turtschaninovii Root Extract, Coptis Japonica Root Extract , Machilus Thunbergii Bark Extract, rh-Oligopeptide-2, rh-Polypeptide-1, rh-Polypeptide-3
- 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 IDEBANONE
niacinamide, adenosine creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71975-040 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) Dimethicone (UNII: 92RU3N3Y1O) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71975-040-02 1 in 1 CARTON 01/02/2018 1 NDC:71975-040-01 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 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(71975-040)
