NDC11 80971010201
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 |
|---|---|
| 80971-0102-01 | 80971-0102 |
| 80971-0102-1 | 80971-0102 |
| 80971-102-01 | 80971-102 |
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 |
|---|---|---|---|---|---|---|
| Protect Prevent Daily Mineral Sunscreen Broad Spectrum SPF30 | TITANIUM DIOXIDE, ZINC OXIDE | Norwex Usa, Inc. | f527a8c5-b05e-5f3c-e053-2995a90aa1a3 | 2025-11-20 | Warnings | 80971-102-01 80971-102 80971010201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.