NDC11 85241006100
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 |
|---|---|
| 85241-0061-0 | 85241-0061 |
| 85241-0061-00 | 85241-0061 |
| 85241-061-00 | 85241-061 |
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 |
|---|---|---|---|---|---|---|
| Timesavvy Hybrid XL Cushion Sun Serum SPF 50 | HOMOSALATE, OCTISALATE, OCTOCRYLENE, ZINC OXIDE | ProBetter USA, Inc. | 82a22071-f1bd-4fab-b929-8a00ef18f0d9 | 2026-05-31 | Warnings | 85241-061-00 85241-061 85241006100 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.