NDC11 87846000120
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 |
|---|---|
| 87846-0001-20 | 87846-0001 |
| 87846-001-20 | 87846-001 |
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 |
|---|---|---|---|---|---|---|
| Freshen Up Holiday mint | SODIUM FLUORIDE | Dabur India Limited | 56aaa9f5-7eac-11d9-e063-6294a90af3a8 | 2026-07-15 | Warnings | 87846-001-20 87846-001 87846000120 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.