NDC11 50804074903
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 |
|---|---|
| 50804-0749-03 | 50804-0749 |
| 50804-0749-3 | 50804-0749 |
| 50804-749-03 | 50804-749 |
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 |
|---|---|---|---|---|---|---|
| Salicylic Acid | CORN AND CALLUS REMOVER | Geiss, Destin & Dunn, Inc. | 21b8d34d-1127-4b0d-b853-0349f25cc91f | 2025-10-08 | Warnings | 50804-749-03 50804-749 50804074903 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.