NDC11 56104090601
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 |
|---|---|
| 56104-0906-01 | 56104-0906 |
| 56104-0906-1 | 56104-0906 |
| 56104-906-01 | 56104-906 |
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 |
|---|---|---|---|---|---|---|
| Medicated Athletes Foot Powder | MICONAZOLE NITRATE | Premier Brands of America Inc. | 38cc0c66-82b5-bac4-e063-6294a90a23f0 | 2026-04-23 | Warnings | 56104-906-01 56104-906 56104090601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.