NDC11 56104001304
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 |
|---|---|
| 56104-0013-04 | 56104-0013 |
| 56104-0013-4 | 56104-0013 |
| 56104-013-04 | 56104-013 |
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 | CALLUS REMOVERS | Premier Brands of America Inc. | 0b637f58-5604-454d-99ba-24115113ac3d | 2026-05-18 | Warnings | 56104-013-04 56104-013 56104001304 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.