NDC11 73928005001
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 |
|---|---|
| 73928-0050-01 | 73928-0050 |
| 73928-0050-1 | 73928-0050 |
| 73928-050-01 | 73928-050 |
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 |
|---|---|---|---|---|---|---|
| BRUSH BUDDIES SQUISHMALLOWS ANTICAVITY FLUORIDE MINT FALVOR | SODIUM FLUORIDE | Kingkey MBC Life Technology Group co., LTD | 1eb04296-ecb1-3ccc-e063-6294a90a9bda | 2025-12-11 | Warnings | 73928-050-01 73928-050 73928005001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.