NDC11 37000086203
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 |
|---|---|
| 37000-0862-03 | 37000-0862 |
| 37000-0862-3 | 37000-0862 |
| 37000-862-03 | 37000-862 |
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 3D White Luxe Diamond Strong | SODIUM FLUORIDE | The Procter & Gamble Manufacturing Company | c1420129-5460-4900-ac9a-356d2d7c60a2 | 2026-01-21 | Warnings | 37000-862-03 37000-862 37000086203 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.