NDC11 71399007104
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 |
|---|---|
| 71399-0071-04 | 71399-0071 |
| 71399-0071-4 | 71399-0071 |
| 71399-071-04 | 71399-071 |
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 |
|---|---|---|---|---|---|---|
| MICONAZOLE Nitrate 2% | MICONAZOLE NITRATE | Akron Pharma Inc. | 8933f939-098a-4257-8d9c-4d5c3240e9a6 | 2025-01-10 | Warnings | 71399-0071-4 71399-0071 71399007104 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.