NDC11 76151024101
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 |
|---|---|
| 76151-0241-01 | 76151-0241 |
| 76151-0241-1 | 76151-0241 |
| 76151-241-01 | 76151-241 |
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 |
|---|---|---|---|---|---|---|
| Boscia Daily Defense Sunscreen Broad Spectrum SPF 50 PA | OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE | Boscia LLC | 2a6b507f-0967-46e1-8360-0003772f1bdb | 2023-12-12 | Warnings | 76151-241-01 76151-241 76151024101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.