NDC11 52000040635
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 |
|---|---|
| 52000-0406-35 | 52000-0406 |
| 52000-406-35 | 52000-406 |
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 |
|---|---|---|---|---|---|---|
| Universal Rubbing Alcohol | ISOPROPYL ALCOHOL | Universal Distribution Center LLC | 183efdc2-cf3e-4f06-b292-0cfd097418b3 | 2026-02-23 | Warnings | 52000-406-35 52000-406 52000040635 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.