United States · FDA National Drug Code directory
Multitol-M
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 59088-005_163fdc9e-a406-c3ee-e063-6294a90afd49
- Product NDC
- 59088-005
- Form
- TABLET
- Composition / generic term
- Multivitamin, Folate
- Labeler
- PureTek Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20240417
- Source listing expiry
- 20261231
Source-listed ingredients
- .ALPHA.-TOCOPHEROL ACETATE, DL- — 13.5 mg/1
- MAGNESIUM OXIDE — 200 mg/1
- CHROMIUM NICOTINATE — 35 ug/1
- PYRIDOXINE HYDROCHLORIDE — 20 mg/1
- MOLYBDENUM — 45 ug/1
- SELENIUM — 55 ug/1
- CHOLECALCIFEROL — 20 ug/1
- RIBOFLAVIN — 3.4 mg/1
- NIACINAMIDE — 20 mg/1
- ASCORBIC ACID — 120 mg/1
- LEVOMEFOLATE CALCIUM — 2040 ug/1
- METHYLCOBALAMIN — 8 ug/1
- CALCIUM CARBONATE — 200 mg/1
- VITAMIN A ACETATE — 1500 ug/1
- THIAMINE MONONITRATE — 3 mg/1
- ZINC OXIDE — 25 mg/1
- MANGANESE SULFATE — 2.3 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE, PLASTIC (59088-005-54) · 59088-005-54
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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