NDC11 37000096547
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 |
|---|---|
| 37000-0965-47 | 37000-0965 |
| 37000-965-47 | 37000-965 |
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 |
|---|---|---|---|---|---|---|
| Burts Bees Charcoal Peppermint | SODIUM FLUORIDE | Procter & Gamble Manufacturing Company | a343853e-4968-2753-e053-2995a90ab152 | 2026-02-02 | Warnings | 37000-965-47 37000-965 37000096547 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.