NDC11 42485000501
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 |
|---|---|
| 42485-0005-01 | 42485-0005 |
| 42485-0005-1 | 42485-0005 |
| 42485-005-01 | 42485-005 |
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 |
|---|---|---|---|---|---|---|
| Broad Spectrum SPF 30 Up The Anti | TITANIUM DIOXIDE, ZINC OXIDE | Biopelle, Inc. | 37506766-370e-4ae4-8dbe-915a763e7c55 | 2023-12-12 | Warnings | 42485-005-01 42485-005 42485000501 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.