Label: NATAFORT- ascorbic acid, cholecalciferol, .alpha.-tocopherol acetate, dl-, thiamine mononitrate, riboflavin, niacinamide, pyridoxine hydrochloride, folic acid, cyanocobalamin, and iron tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 0178-0716-90 - Packager: Mission Pharmacal Company
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated August 10, 2011
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DESCRIPTION
NataFort® is a prescription prenatal/postnatal multivitamin/mineral supplement. The tablet is white, coated, and oval in shape, and is debossed "N1" on one side and is blank on the other.
Each prenatal tablet contains: Vitamin C (Ascorbic acid) 120 mg Vitamin D3 (Cholecalciferol) 400 IU Vitamin E (dl-alpha tocoperyl acetate) 11 IU Thiamin (Vitamin B1) 2 mg Riboflavin (Vitamin B2) 3 mg Niacinamide (Vitamin B3) 20 mg Vitamin B6 (Pyridoxine HCl) 10 mg Folic Acid 1 mg Vitamin B12 (Cyanocobalamin) 12 mcg Iron (Ferrous fumarate, carbonyl iron) 60 mg - INDICATIONS
- CONTRAINDICATIONS
- BOXED WARNING (What is this?)
- WARNING
- PRECAUTIONS
- ADVERSE REACTIONS
- DOSAGE AND ADMINISTRATION
- STORAGE AND HANDLING
- HOW SUPPLIED
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 90 Tablet Bottle Label
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INGREDIENTS AND APPEARANCE
NATAFORT
ascorbic acid, cholecalciferol, .alpha.-tocopherol acetate, dl-, thiamine mononitrate, riboflavin, niacinamide, pyridoxine hydrochloride, folic acid, cyanocobalamin, and iron tabletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0178-0716 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Ascorbic acid (UNII: PQ6CK8PD0R) (Ascorbic acid - UNII:PQ6CK8PD0R) Ascorbic acid 120 mg Cholecalciferol (UNII: 1C6V77QF41) (Cholecalciferol - UNII:1C6V77QF41) Cholecalciferol 400 [iU] .alpha.-tocopherol acetate, dl- (UNII: WR1WPI7EW8) (.alpha.-tocopherol acetate, dl- - UNII:WR1WPI7EW8) .alpha.-tocopherol acetate, dl- 11 [iU] Thiamine mononitrate (UNII: 8K0I04919X) (Thiamine - UNII:X66NSO3N35) Thiamine mononitrate 2 mg Riboflavin (UNII: TLM2976OFR) (Riboflavin - UNII:TLM2976OFR) Riboflavin 3 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 Cyanocobalamin (UNII: P6YC3EG204) (Cyanocobalamin - UNII:P6YC3EG204) Cyanocobalamin 12 ug Iron (UNII: E1UOL152H7) (Iron - UNII:E1UOL152H7) Iron 60 mg Inactive Ingredients Ingredient Name Strength polyethylene glycols (UNII: 3WJQ0SDW1A) calcium carbonate (UNII: H0G9379FGK) povidone (UNII: FZ989GH94E) cellulose, microcrystalline (UNII: OP1R32D61U) croscarmellose sodium (UNII: M28OL1HH48) titanium dioxide (UNII: 15FIX9V2JP) magnesium silicate (UNII: 9B9691B2N9) vitamin a palmitate (UNII: 1D1K0N0VVC) magnesium stearate (UNII: 70097M6I30) ethyl vanillin (UNII: YC9ST449YJ) Dimethylaminoethyl methacrylate - butyl methacrylate - methyl methacrylate copolymer (UNII: 905HNO1SIH) Product Characteristics Color WHITE Score no score Shape OVAL Size 14mm Flavor Imprint Code N1 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0178-0716-90 90 in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved drug other 08/25/2011 Labeler - Mission Pharmacal Company (008117095) Establishment Name Address ID/FEI Business Operations Mission Pharmacal Company 927726893 MANUFACTURE