NDC11 52000044304
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 |
|---|---|
| 52000-0443-04 | 52000-0443 |
| 52000-0443-4 | 52000-0443 |
| 52000-443-04 | 52000-443 |
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 |
|---|---|---|---|---|---|---|
| ORAL PAIN RELIEF | BENZOCAINE | Universal Distribution Center LLC | e276ba37-46fb-4ed9-9ee1-c08a2a89704a | 2026-01-20 | Warnings | 52000-443-04 52000-443 52000044304 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.