NDC11 47682032102
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 |
|---|---|
| 47682-0321-02 | 47682-0321 |
| 47682-0321-2 | 47682-0321 |
| 47682-321-02 | 47682-321 |
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 |
|---|---|---|---|---|---|---|
| Pain Relief | ANALGESIC MENTHOL | Unifirst First Aid Corporation | 8162d22d-04c0-de07-e053-2991aa0a9975 | 2025-09-08 | Warnings | 47682-321-02 47682-321 47682032102 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.