NDC11 59088001554
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 59088-0015-54 | 59088-0015 |
| 59088-015-54 | 59088-015 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Flotrex | MULTIVITAMINS, SODIUM FLUORIDE 0.5 MG | PureTek Corporation | 2e0e51f3-ee2c-540d-e063-6294a90a9275 | 2025-07-14 | Warnings, Adverse reactions | 59088-015-54 59088-015 59088001554 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.