NDC11 79481061101
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 |
|---|---|
| 79481-0611-01 | 79481-0611 |
| 79481-0611-1 | 79481-0611 |
| 79481-611-01 | 79481-611 |
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 |
|---|---|---|---|---|---|---|
| Medicated Callus Removers Extra Thick | SALICYLIC ACID | Meijer Distribution Inc | 039bcd7d-9a71-a1aa-e063-6294a90a0953 | 2026-01-02 | Warnings | 79481-0611-1 79481-0611 79481061101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.