United States · FDA National Drug Code directory
Diatrol
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
- 59088-162_5681738a-443b-7127-e063-6394a90a01a2
- Product NDC
- 59088-162
- Form
- TABLET
- Composition / generic term
- vitamins and mineral
- Labeler
- PureTek Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20240126
- Source listing expiry
- 20271231
Source-listed ingredients
- BIOTIN — 30 ug/1
- VANADYL SULFATE — 15 mg/1
- CHROMIUM NICOTINATE — 200 ug/1
- GYMNEMA SYLVESTRE LEAF — 100 mg/1
- ARGININE HYDROCHLORIDE — 60 ug/1
- .ALPHA.-TOCOPHEROL ACETATE, DL- — 13.5 mg/1
- PHYTONADIONE — 90 ug/1
- VITAMIN A — 900 ug/1
- ASCORBIC ACID — 50 mg/1
- CHOLECALCIFEROL — 18.75 ug/1
- PYRIDOXINE HYDROCHLORIDE — 8 mg/1
- THIAMINE MONONITRATE — 4 mg/1
- RIBOFLAVIN — 4 mg/1
- NIACIN — 24 mg/1
- LEVOMEFOLATE CALCIUM — 1000 ug/1
- METHYLCOBALAMIN — 8 ug/1
- PANTOTHENIC ACID — 8 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE, PLASTIC (59088-162-54) · 59088-162-54
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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