NDC11 73067087004
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 |
|---|---|
| 73067-0870-04 | 73067-0870 |
| 73067-0870-4 | 73067-0870 |
| 73067-870-04 | 73067-870 |
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 |
|---|---|---|---|---|---|---|
| NERVE REVERSE PAIN RELIEF | MENTHOL | Pogue Medical Services | da97bcc6-5aa8-48e2-a2c2-c937745bf6d3 | 2025-06-23 | Warnings | 73067-870-04 73067-870 73067087004 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.