NDC11 50390021530
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 |
|---|---|
| 50390-0215-30 | 50390-0215 |
| 50390-215-30 | 50390-215 |
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 Exact Fit Longwearing Foundation Shade Sand L2W1 | TITANIUM DIOXIDE | Amway Corp | 4345cdf6-e220-4e7c-8abd-da59d2b7db84 | 2026-01-09 | Warnings | 50390-215-30 50390-215 50390021530 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.