NDC11 52000080101
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 |
|---|---|
| 52000-0801-01 | 52000-0801 |
| 52000-0801-1 | 52000-0801 |
| 52000-801-01 | 52000-801 |
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 |
|---|---|---|---|---|---|---|
| Isopropyl Rubbing Alcohol | ISOPROPYL ALCOHOL | Universal Distribution Center LLC | 2f982aef-4f46-aa85-e063-6394a90a52b1 | 2025-03-05 | Warnings | 52000-801-01 52000-801 52000080101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.