NDC11 58602060705
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 |
|---|---|
| 58602-0607-05 | 58602-0607 |
| 58602-0607-5 | 58602-0607 |
| 58602-607-05 | 58602-607 |
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 |
|---|---|---|---|---|---|---|
| MINOXIDIL 5% (FOR WOMEN) | MINOXIDIL | Aurohealth LLC | dbda95f2-11a8-4b2f-af45-b791342fff70 | 2026-01-22 | Warnings | 58602-607-05 58602-607 58602060705 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.