NDC11 50845005701
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 |
|---|---|
| 50845-0057-01 | 50845-0057 |
| 50845-0057-1 | 50845-0057 |
| 50845-057-01 | 50845-057 |
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 |
|---|---|---|---|---|---|---|
| Wart Free | ANTIMONIUM CRUDUM, BAPTISIA TINCTORIA, CAUSTICUM, NITRICUM ACIDUM, THUJA OCCIDENTALIS, | Liddell Laboratories, Inc. | e6895ca5-08a7-4ab4-b6bf-4d2434831ab4 | 2018-11-05 | Warnings | 50845-0057-1 50845-0057 50845005701 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.