NDC11 59883071804
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 |
|---|---|
| 59883-0718-04 | 59883-0718 |
| 59883-0718-4 | 59883-0718 |
| 59883-718-04 | 59883-718 |
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 |
|---|---|---|---|---|---|---|
| Kids Kare | SODIUM FLUORIDE | DEN-MAT HOLDINGS, LLC. | 66d6b20f-d0ff-4dfe-e053-2991aa0a99ca | 2024-12-31 | Warnings | 59883-718-04 59883-718 59883071804 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.