NDC11 74680020186
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 |
|---|---|
| 74680-0201-86 | 74680-0201 |
| 74680-201-86 | 74680-201 |
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 |
|---|---|---|---|---|---|---|
| Wipex | ANTIBACTERIAL WIPE | Unico International Trading Corporation | 261c7b8f-4adc-72ec-e063-6394a90a9211 | 2026-01-08 | Warnings | 74680-201 |
| Wipex | ANTIBACTERIAL WIPE | Unico International Trading Corporation | 144453a2-8335-77be-e063-6394a90ab676 | 2026-01-08 | Warnings | 74680-201-86 74680-201 74680020186 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.