NDC11 85883020350
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 |
|---|---|
| 85883-0203-50 | 85883-0203 |
| 85883-203-50 | 85883-203 |
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 |
|---|---|---|---|---|---|---|
| Advanced Formula Tinted | TITANIUM DIOXIDE, ZINC OXIDE | CR KEEFE ENTERPRISES, INC. | 3984c4b7-94ee-2a8e-e063-6294a90ac24f | 2025-12-15 | 85883-203 | |
| Advanced Formula Tinted | TITANIUM DIOXIDE, ZINC OXIDE | CR KEEFE ENTERPRISES, INC. | 3984920a-feb9-169c-e063-6394a90a9568 | 2025-12-15 | 85883-203-50 85883-203 85883020350 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.