NDC11 67091039004
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 |
|---|---|
| 67091-0390-04 | 67091-0390 |
| 67091-0390-4 | 67091-0390 |
| 67091-390-04 | 67091-390 |
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 |
|---|---|---|---|---|---|---|
| Tolnaftate | FOOT ODOR CONTROL POWDER SPRAY | Winco Foods, LLC | cc257a18-247f-c787-e053-2a95a90a075a | 2025-12-16 | Warnings | 67091-390-04 67091-390 67091039004 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.