NDC11 51009090240
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 |
|---|---|
| 51009-0902-40 | 51009-0902 |
| 51009-902-40 | 51009-902 |
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 |
|---|---|---|---|---|---|---|
| TOMS OF MAINE WHOLE CARE WINTERMINT | SODIUM MONOFLUOROPHOSPHATE | Tom's of Maine, Inc. | d5e1396e-0253-4ec0-a9ff-b61bda70de35 | 2026-08-10 | Warnings | 51009-902-40 51009-902 51009090240 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.