NDC11 52000041803
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 |
|---|---|
| 52000-0418-03 | 52000-0418 |
| 52000-0418-3 | 52000-0418 |
| 52000-418-03 | 52000-418 |
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 |
|---|---|---|---|---|---|---|
| ANTIFUNGAL FOOT | TOLNAFTATE | Universal Distribution Center LLC | 10579848-5793-4d72-ad5f-62d191c71074 | 2024-07-16 | Warnings | 52000-418-03 52000-418 52000041803 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.