NDC11 85334020850
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 |
|---|---|
| 85334-0208-50 | 85334-0208 |
| 85334-208-50 | 85334-208 |
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 |
|---|---|---|---|---|---|---|
| Satin Tint | ZINC OXIDE | Brent Loftis, D.O., Inc., A California Medical Corporation | 35920108-7f8a-27d4-e063-6294a90a0ef6 | 2025-12-12 | 85334-208-50 85334-208 85334020850 | |
| Satin Tint | ZINC OXIDE | Brent Loftis, D.O., Inc., A California Medical Corporation | 359684cf-ca11-f9af-e063-6394a90ac4c1 | 2025-12-12 | 85334-208 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.