NDC11 50742053901
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 |
|---|---|
| 50742-0539-01 | 50742-0539 |
| 50742-0539-1 | 50742-0539 |
| 50742-539-01 | 50742-539 |
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 |
|---|---|---|---|---|---|---|
| Dehydrated Alcohol | DEHYDRATED ALCOHOL | Ingenus Pharmaceuticals, LLC | 1d5ec6f9-d58f-4651-a4a1-93fec13fd438 | 2025-07-11 | Warnings, Adverse reactions | 50742-539-01 50742-539 50742053901 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.