NDC11 85998000101
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 |
|---|---|
| 85998-0001-01 | 85998-0001 |
| 85998-0001-1 | 85998-0001 |
| 85998-001-01 | 85998-001 |
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 |
|---|---|---|---|---|---|---|
| SUNSCREEN SPF50 | ETHYLHEXYL METHOXYCINNAMATE, OCTOCRYLENE, TITANIUM DIOXIDE | Guangzhou Tinsun Biotechnology Company Limited | 3bc1c6e9-1dd5-d7c6-e063-6394a90ad89e | 2025-08-07 | Warnings | 85998-001-01 85998-001 85998000101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.