NDC11 79073000304
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 |
|---|---|
| 79073-0003-04 | 79073-0003 |
| 79073-0003-4 | 79073-0003 |
| 79073-003-04 | 79073-003 |
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 |
|---|---|---|---|---|---|---|
| natouch | MICONAZOLE | Natouch LLC | 55210a9d-6c47-4fc7-e063-6294a90a3653 | 2026-06-25 | Warnings | 79073-003-04 79073-003 79073000304 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.