United States · FDA National Drug Code directory
Flotrex
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
- 59088-017_39ed4312-2ed6-cb13-e063-6294a90aefc9
- Product NDC
- 59088-017
- Form
- TABLET, CHEWABLE
- Composition / generic term
- Multivitamins, Sodium Fluoride 0.25 mg
- Labeler
- PureTek Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20250319
- Source listing expiry
- 20261231
Source-listed ingredients
- SODIUM FLUORIDE — .25 mg/1
- VITAMIN A — 750 ug/1
- ASCORBIC ACID — 24 mg/1
- SODIUM ASCORBATE — 36 mg/1
- CHOLECALCIFEROL — 10 ug/1
- .ALPHA.-TOCOPHEROL ACETATE, DL- — 6.75 mg/1
- THIAMINE MONONITRATE — 1.05 mg/1
- RIBOFLAVIN — 1.2 mg/1
- NIACINAMIDE — 13.5 mg/1
- PYRIDOXINE HYDROCHLORIDE — 1.05 mg/1
- FOLIC ACID — 300 ug/1
- CYANOCOBALAMIN — 4.5 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (59088-017-54) · 59088-017-54
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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