warnings
Avoid eye contact, if occurs rinse eyes thoroughly with water. If develop any allergic reaction, discontinue its use. warning
hair treatment
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- hair treatment
- Generic name
- MINOXIDIL
- Manufacturer
- LABORATORIO MK SRL
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 3cf60fba-8c8d-d56f-e063-6294a90a344b
- SPL ID
- 3d84eb2d-f0a8-a21c-e063-6294a90aeef5
- Version
- 2
- Effective date
- 2025-08-29
- Source export date
- 2026-10-12
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 03:10:20
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | 505G(a)(3) | openfda.application_number | |
| brand name | hair treatment | openfda.brand_name | |
| generic name | MINOXIDIL | openfda.generic_name | |
| manufacturer name | LABORATORIO MK SRL | openfda.manufacturer_name | |
| ndc | package | 87022-009-25 | openfda.package_ndc |
| ndc | product | 87022-009 | openfda.product_ndc |
| ndc11 | package | 87022000925 | derived:openfda.package_ndc |
| spl id | 3d84eb2d-f0a8-a21c-e063-6294a90aeef5 | id | |
| spl set id | 3cf60fba-8c8d-d56f-e063-6294a90a344b | set_id | |
| unii | 5965120SH1 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.