NDC11 83881040301
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 |
|---|---|
| 83881-0403-01 | 83881-0403 |
| 83881-0403-1 | 83881-0403 |
| 83881-403-01 | 83881-403 |
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 |
|---|---|---|---|---|---|---|
| LidoPro | LIDOCAINE AND MENTHOL | Clinic Pharma | cdfd6b39-b430-4e95-a0f7-682cf3d78b52 | 2026-07-28 | Warnings | 83881-403-01 83881-403 83881040301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.