NDC11 66800364106
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 |
|---|---|
| 66800-3641-06 | 66800-3641 |
| 66800-3641-6 | 66800-3641 |
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 |
|---|---|---|---|---|---|---|
| Coppertone Defend and Clear | OCTINOXATE, OCTISALATE, ZINC OXIDE | Beiersdorf Inc | baaec6a9-2c60-2d11-e053-2a95a90abca7 | 2025-12-31 | Warnings | 66800-3641-6 66800-3641 66800364106 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.