NDC11 82038000504
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 |
|---|---|
| 82038-0005-04 | 82038-0005 |
| 82038-0005-4 | 82038-0005 |
| 82038-005-04 | 82038-005 |
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 |
|---|---|---|---|---|---|---|
| Protectif Deep Tint | ZINC OXIDE AND TITANIUM DIOXIDE | Derma Research Group Inc. | 19b19023-1340-6609-e063-6394a90a6eaf | 2024-05-30 | Warnings | 82038-005-04 82038-005 82038000504 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.