NDC11 71014002900
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 |
|---|---|
| 71014-0029-0 | 71014-0029 |
| 71014-0029-00 | 71014-0029 |
| 71014-029-00 | 71014-029 |
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 |
|---|---|---|---|---|---|---|
| VERTRA Premium Suncare SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | Eai-Jr286, Inc. | 720ca725-24ca-4b59-b640-afa983238692 | 2023-11-05 | Warnings | 71014-029-00 71014-029 71014002900 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.