NDC11 82038000603
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 |
|---|---|
| 82038-0006-03 | 82038-0006 |
| 82038-0006-3 | 82038-0006 |
| 82038-006-03 | 82038-006 |
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 Fair Tint | ZINC OXIDE AND TITANIUM DIOXIDE | Derma Research Group Inc. | 1a8c8804-1d6b-b5a5-e063-6394a90a1260 | 2024-06-18 | Warnings | 82038-006-03 82038-006 82038000603 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.