NDC11 37000000857
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 |
|---|---|
| 37000-0008-57 | 37000-0008 |
| 37000-008-57 | 37000-008 |
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 |
|---|---|---|---|---|---|---|
| Crest Tartar Protection | SODIUM FLUORIDE | The Procter & Gamble Manufacturing Company | 85477763-1db5-482f-90e5-e71f5c1b4765 | 2026-01-08 | Warnings | 37000-008-57 37000-008 37000000857 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.