NDC11 75936066302
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 |
|---|---|
| 75936-0663-02 | 75936-0663 |
| 75936-0663-2 | 75936-0663 |
| 75936-663-02 | 75936-663 |
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 |
|---|---|---|---|---|---|---|
| Mineral Mattescreen SPF 40 - Golden Hour | TITANIUM DIOXIDE, ZINC OXIDE | Supergoop, LLC | c2398820-f003-707f-e053-2a95a90a6929 | 2026-06-04 | Warnings | 75936-663-02 75936-663 75936066302 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.