NDC11 87398000101
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 |
|---|---|
| 87398-0001-01 | 87398-0001 |
| 87398-0001-1 | 87398-0001 |
| 87398-001-01 | 87398-001 |
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 |
|---|---|---|---|---|---|---|
| LIVFRESH GUM PROTECT | STANNOUS FLUORIDE | Livionex Inc. | 1da7dcf9-e675-4b4b-8286-bdaa6e59eb0f | 2026-02-02 | Warnings | 87398-001-01 87398-001 87398000101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.