NDC11 37000087638
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 |
|---|---|
| 37000-0876-38 | 37000-0876 |
| 37000-876-38 | 37000-876 |
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 Radiant Mint | SODIUM FLUORIDE | The Procter & Gamble Manufacturing Company | f3dd7a34-a0d8-4ac6-bbd1-7c3b86187a57 | 2026-01-08 | Warnings | 37000-876-38 37000-876 37000087638 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.