NDC11 50390022700
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 |
|---|---|
| 50390-0227-0 | 50390-0227 |
| 50390-0227-00 | 50390-0227 |
| 50390-227-00 | 50390-227 |
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 |
|---|---|---|---|---|---|---|
| Artistry Youth Xtend Lifting Smoothing Foundation Shade Buff L1W1 | OCTINOXATE, OXYBENZONE | Amway Corp | 11a8cc16-33f1-43d1-9f35-aa0f6e70adf6 | 2023-10-22 | Warnings | 50390-227-00 50390-227 50390022700 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.