NDC11 60771003201
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 |
|---|---|
| 60771-0032-01 | 60771-0032 |
| 60771-0032-1 | 60771-0032 |
| 60771-032-01 | 60771-032 |
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 |
|---|---|---|---|---|---|---|
| Pure velocity MINERAL SUNSCREEN SPF 50 | TITANIUM DIOXIDE,ZINC OXIDE | Guangzhou Haishi Biological Technology Co., Ltd. | 4003047b-bc55-bb11-e063-6294a90aa433 | 2025-09-30 | Warnings | 60771-0032-1 60771-0032 60771003201 |