NDC11 63742009802
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 |
|---|---|
| 63742-0098-02 | 63742-0098 |
| 63742-0098-2 | 63742-0098 |
| 63742-098-02 | 63742-098 |
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 |
|---|---|---|---|---|---|---|
| Fungus Master | MICONAZOLE NITRATE | Clinical Resolution Laboratory, Inc. | 36eb334e-246b-249f-e063-6294a90ab811 | 2025-06-06 | Warnings | 63742-098-02 63742-098 63742009802 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.