NDC11 82939000002
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 |
|---|---|
| 82939-000-02 | 82939-000 |
| 82939-0000-02 | 82939-0000 |
| 82939-0000-2 | 82939-0000 |
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 |
|---|---|---|---|---|---|---|
| ORCA Complete Menthol Pain Reliever | MENTHOL | ORCA Products, LLC | 99990e27-d66b-4d61-97f2-6a76066eb8b8 | 2023-12-08 | Warnings | 82939-000-02 82939-000 82939000002 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.