NDC11 81522095601
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 |
|---|---|
| 81522-0956-01 | 81522-0956 |
| 81522-0956-1 | 81522-0956 |
| 81522-956-01 | 81522-956 |
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 | LIQUID CORN AND CALLUS REMOVER | FSA Store Inc. | 3cd18e4c-26c1-1548-e063-6294a90acdb0 | 2025-10-08 | Warnings | 81522-956-01 81522-956 81522095601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.