NDC11 85248002201
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 |
|---|---|
| 85248-0022-01 | 85248-0022 |
| 85248-0022-1 | 85248-0022 |
| 85248-022-01 | 85248-022 |
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 |
|---|---|---|---|---|---|---|
| LXHUKU WART REMOVER | SALICYLIC ACID 17% WART REMOVER | Jiangxi Yudexi Pharmaceutical Co., LTD | 4982e90f-cdc4-6364-e063-6294a90a8e52 | 2026-01-29 | Warnings | 85248-022-01 85248-022 85248002201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.