NDC11 56104025510
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 |
|---|---|
| 56104-0255-10 | 56104-0255 |
| 56104-255-10 | 56104-255 |
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 |
|---|---|---|---|---|---|---|
| Premier Solutions Liquid Corn and Callus Remover | SALICYLIC ACID | Premier Brands of America Inc. | e16d0256-1151-8394-e053-2995a90ab56c | 2026-05-08 | Warnings | 56104-255-10 56104-255 56104025510 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.