NDC11 52000003825
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 |
|---|---|
| 52000-0038-25 | 52000-0038 |
| 52000-038-25 | 52000-038 |
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 |
|---|---|---|---|---|---|---|
| Medicated Body | MENTHOL AND ZINC OXIDE | Universal Distribution Center LLC | 2a59a847-cc7a-42cf-b49a-92e7254c1629 | 2024-06-19 | Warnings | 52000-038-25 52000-038 52000003825 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.