NDC11 85212000101
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 |
|---|---|
| 85212-0001-01 | 85212-0001 |
| 85212-0001-1 | 85212-0001 |
| 85212-001-01 | 85212-001 |
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 |
|---|---|---|---|---|---|---|
| FluMisch Minoxidil Foam | MINOXIDIL,BIOTIN | Beijing JUNGE Technology Co., Ltd. | 2d34dc32-47d8-590d-e063-6294a90a2f2d | 2025-02-02 | Warnings | 85212-0001-1 85212-0001 85212000101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.