Label: VITAL-D RX- multi vitamin/mineral supplement containing vitamin c, vitamin d, vitamin e, thiamin, riboflavin, niacin, pyridoxine, folic acid, cobalamin, biotin, pantothenic acid, selenium and zinc tablet, coated
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Contains inactivated NDC Code(s)
NDC Code(s): 59528-1988-1 - Packager: Nephro-Tech, Inc.
- Category: HUMAN PRESCRIPTION DRUG LABEL
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Drug Label Information
Updated July 14, 2021
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INGREDIENTS AND APPEARANCE
VITAL-D RX
multi vitamin/mineral supplement containing vitamin c, vitamin d, vitamin e, thiamin, riboflavin, niacin, pyridoxine, folic acid, cobalamin, biotin, pantothenic acid, selenium and zinc tablet, coatedProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:59528-1988 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R) ASCORBIC ACID 60 mg CHOLECALCIFEROL (UNII: 1C6V77QF41) (CHOLECALCIFEROL - UNII:1C6V77QF41) CHOLECALCIFEROL 2000 [iU] TOCOPHEROL (UNII: R0ZB2556P8) (TOCOPHEROL - UNII:R0ZB2556P8) TOCOPHEROL 35 [iU] THIAMINE (UNII: X66NSO3N35) (THIAMINE ION - UNII:4ABT0J945J) THIAMINE 1.5 mg RIBOFLAVIN (UNII: TLM2976OFR) (RIBOFLAVIN - UNII:TLM2976OFR) RIBOFLAVIN 1.7 mg NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 20 mg PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV) (PYRIDOXINE - UNII:KV2JZ1BI6Z) PYRIDOXINE HYDROCHLORIDE 10 mg FOLIC ACID (UNII: 935E97BOY8) (FOLIC ACID - UNII:935E97BOY8) FOLIC ACID 1 mg COBALAMIN (UNII: 8406EY2OQA) (COBALAMIN - UNII:8406EY2OQA) COBALAMIN 6 ug BIOTIN (UNII: 6SO6U10H04) (BIOTIN - UNII:6SO6U10H04) BIOTIN 300 ug PANTOTHENIC ACID (UNII: 19F5HK2737) (PANTOTHENIC ACID - UNII:19F5HK2737) PANTOTHENIC ACID 10 mg ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 12.5 mg SELENOMETHIONINE (UNII: 964MRK2PEL) (SELENOMETHIONINE - UNII:964MRK2PEL) SELENOMETHIONINE 70 ug Product Characteristics Color white Score no score Shape OVAL Size 16mm Flavor Imprint Code D3 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59528-1988-1 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/01/2007 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 11/01/2007 Labeler - Nephro-Tech, Inc. (878520485) Registrant - Nephro-Tech, Inc. (878520485) Establishment Name Address ID/FEI Business Operations LGM Pharma 117549200 manufacture(59528-1988)
