Home NDC 59088-139 Vitalux
Product NDC 59088-139
11-digit product format 590880139
Labeler code 59088
Product ID 59088-139_52d5fd35-3a68-5edd-e063-6394a90aba81
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Multivitamin
Dosage form TABLET
Route ORAL
Labeler PureTek Corporation
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2026-06-03
Substance MAGNESIUM OXIDE; MANGANESE SULFATE; VITAMIN A ACETATE; ASCORBIC ACID; CHOLECALCIFEROL; .ALPHA.-TOCOPHEROL ACETATE, DL-; THIAMINE MONONITRATE; RIBOFLAVIN; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; LEVOMEFOLIC ACID; CYANOCOBALAMIN; CALCIUM CARBONATE; FERROUS FUMARATE; ZINC OXIDE; MOLYBDENUM; CHOLINE BITARTRATE; SELENIUM; CHROMIUM NICOTINATE; POTASSIUM IODIDE
Active strength 200; 2.6; 1500; 120; 20; 30; 3; 3.4; 20; 50; 1000; 10; 200; 27; 25; 50; 55; 70; 45; 150 mg/1; mg/1; ug/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; ug/1; mg/1; mg/1; mg/1; ug/1; mg/1; ug/1; ug/1; ug/1
Pharmacologic classes Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Folate Analog [EPC], Folic Acid [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Magnetic Resonance Contrast Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Paramagnetic Contrast Agent [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE], Vitamin A [CS], Vitamin A [EPC], Vitamin B 12 [CS], Vitamin B 6 [Chemical/Ingredient], Vitamin B12 [EPC], Vitamin B6 Analog [EPC], Vitamin C [EPC], Vitamin D [CS], Vitamin D [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Vitalux
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MAGNESIUM OXIDE 200 mg/1 MANGANESE SULFATE 2.6 mg/1 VITAMIN A ACETATE 1500 ug/1 ASCORBIC ACID 120 mg/1 CHOLECALCIFEROL 20 ug/1 .ALPHA.-TOCOPHEROL ACETATE, DL- 30 mg/1 THIAMINE MONONITRATE 3 mg/1 RIBOFLAVIN 3.4 mg/1 NIACINAMIDE 20 mg/1 PYRIDOXINE HYDROCHLORIDE 50 mg/1 LEVOMEFOLIC ACID 1000 ug/1 CYANOCOBALAMIN 10 ug/1 CALCIUM CARBONATE 200 mg/1 FERROUS FUMARATE 27 mg/1 ZINC OXIDE 25 mg/1 MOLYBDENUM 50 ug/1 CHOLINE BITARTRATE 55 mg/1 SELENIUM 70 ug/1 CHROMIUM NICOTINATE 45 ug/1 POTASSIUM IODIDE 150 ug/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 20 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Vitalux MULTIVITAMIN PureTek Corporation 52d5eee7-8146-cc62-e063-6394a90a8c3f 2026-06-02 Boxed warning, Adverse reactions Exact identifier ndc (product): 59088-139
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 59088-139-54 59088013954 30 TABLET in 1 BOTTLE, PLASTIC (59088-139-54) 30 tablet 2026-06-03 No No Current