NDC11 87846000713
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 |
|---|---|
| 87846-0007-13 | 87846-0007 |
| 87846-007-13 | 87846-007 |
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 | SODIUM FLUORIDE | DABUR INDIA LIMITED | 56acecd2-6966-2ee4-e063-6394a90a356f | 2026-07-15 | Warnings | 87846-007-13 87846-007 87846000713 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.