NDC11 52000044215
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 |
|---|---|
| 52000-0442-15 | 52000-0442 |
| 52000-442-15 | 52000-442 |
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 |
|---|---|---|---|---|---|---|
| 4% MENTHOL COLD THERAPY | MENTHOL | Universal Distribution Center LLC | 66892993-a755-4584-b2a8-2e8d7ac70593 | 2026-01-08 | Warnings | 52000-442-15 52000-442 52000044215 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.