NDC11 37000044598
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 |
|---|---|
| 37000-0445-98 | 37000-0445 |
| 37000-445-98 | 37000-445 |
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 Complete plus Whitening plus Scope Outlast | SODIUM FLUORIDE | The Procter & Gamble Manufacturing Company | 960e0e3e-10e8-7426-e053-2a95a90a5b02 | 2026-02-12 | Warnings | 37000-445-98 37000-445 37000044598 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.