NDC | 71975-060-01, 71975-060-02 |
Set ID | 8c0f4ba9-2744-4712-81e2-8a20acbba16c |
Category | HUMAN OTC DRUG LABEL |
Packager | Ultra V Co., Ltd |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients: Water, Methylpropanediol, Cprylyl methicone, Coco-Caprylate/Caprate, Stearyl Dimethicone, Niacinamide, Trimethylsiloxysilicate, Diisostearyl malate, Magnesium Sulfate, Iron Oxides(CI 77492), Octadecene, Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, Sythetic Fluorphlogopite, Aminopropyl Dimethicone, Phenoxyethanol, Polymethylsilsesquioxane, Iron Oxides(CI 77491), Disteardimonium hectorite, Fragrance, Alumina, Ethylhexylglycerin, Silica, Iron, oxides(CI 77499), Octyldodecanol, Triethoxycaprylylsilane, Dextrin Palmitate, Xanthan Gum, Adenosine, Portulaca Oleracea Extract, Echium Plantagineum Seed Oil, Tocopheryl Acetate, Dimethicone, Butylene Glycol, Cardiospermum Halicacabum Flower/leaf/vine Extract, Hydroxydecul Ubiquinone, Helianthus Annuus (Sunflower) Seed Oil Unsaponifiables, Tocopherol, Bambusa Arundinacea Stem Extract, Moringa Oleifera Seed Oil, Maltodextrin, Ceramide NP, Persea Gratissima (Avocado) Oil, Copper Tripeptide-1, Saccharide Hydrolysate, Hydrolyzed Vegetable Protein, Alcohol, Caprylic/Capric Triglyceride, 1,2-Hexanediol, Phellinus Linteus Extract, Phellinus Linteus Extract, Hydrogenated Lecithin, Ganoderma Lucidum (Mushroom) Stem Extract, Punica Granatum Extract, Sodium Stearoyl Glutamate, Rosa Damascena Flower Oil, Cordyceps Sinensis Extract, Disodium EDTA, Sodium Ascorbyl Phosphate, Acetyl hexapeptide-8, sh-Oligopeptide-1
- PURPOSE
- WARNINGS
- DESCRIPTION
- QUESTIONS
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ULTRA V IDEBENONE SKINFIT CUSHION
titanium dioxide, octinoxate, zinc oxide powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71975-060 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Titanium Dioxide (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) Titanium Dioxide 1.40 g in 14 g Octinoxate (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) Octinoxate 0.70 g in 14 g Zinc Oxide (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 0.27 g in 14 g Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Methylpropanediol (UNII: N8F53B3R4R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71975-060-02 1 in 1 CARTON 01/02/2018 1 NDC:71975-060-01 14 g in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 01/02/2018 Labeler - Ultra V Co., Ltd (689004748) Registrant - Ultra V Co., Ltd (689004748) Establishment Name Address ID/FEI Business Operations Kolmar Korea Co., Ltd. 689512611 manufacture(71975-060)