warnings
Warnings For external use only. For use by men only. Extremely Flammable : Avoid fire, flame, or smoking during and immediately following application.
MINOXIDIL 5% (FOR MEN)
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
- MINOXIDIL 5% (FOR MEN)
- Generic name
- MINOXIDIL
- Manufacturer
- Aurohealth LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- e6b3b997-cde9-476d-b08c-4d1010456d8b
- SPL ID
- 84225922-895c-4386-b8ef-9b0beb2d1b07
- Version
- 4
- Effective date
- 2026-01-22
- Source export date
- 2026-11-06
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/824fe785252d7061429a95ddb6de517ee399ef628d34e8fdcc3591ded286ae33/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:25:38
| 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 applno | ANDA | 218616 | derived:openfda.application_number |
| application number | ANDA218616 | openfda.application_number | |
| brand name | MINOXIDIL 5% (FOR MEN) | openfda.brand_name | |
| generic name | MINOXIDIL | openfda.generic_name | |
| manufacturer name | Aurohealth LLC | openfda.manufacturer_name | |
| ndc | package | 58602-608-04 | openfda.package_ndc |
| ndc | package | 58602-608-03 | openfda.package_ndc |
| ndc | package | 58602-608-01 | openfda.package_ndc |
| ndc | package | 58602-608-05 | openfda.package_ndc |
| ndc | package | 58602-608-02 | openfda.package_ndc |
| ndc | product | 58602-608 | openfda.product_ndc |
| ndc11 | package | 58602060804 | derived:openfda.package_ndc |
| ndc11 | package | 58602060801 | derived:openfda.package_ndc |
| ndc11 | package | 58602060802 | derived:openfda.package_ndc |
| ndc11 | package | 58602060805 | derived:openfda.package_ndc |
| ndc11 | package | 58602060803 | derived:openfda.package_ndc |
| rxcui | 645146 | openfda.rxcui | |
| spl id | 84225922-895c-4386-b8ef-9b0beb2d1b07 | id | |
| spl set id | e6b3b997-cde9-476d-b08c-4d1010456d8b | 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.