NDC11 83067046300
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 |
|---|---|
| 83067-0463-0 | 83067-0463 |
| 83067-0463-00 | 83067-0463 |
| 83067-463-00 | 83067-463 |
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 |
|---|---|---|---|---|---|---|
| DIRT Pain Relieving Gel | MENTHOL | PURIVITAE, LLC | e43e2cbd-d114-4b11-8baf-7a775881cd97 | 2023-11-06 | Warnings | 83067-463-00 83067-463 83067046300 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.