warnings
Warnings For external use only. Extremely Flammable: Avoid fire, flame, or smoking during and immediately following application.
MINOXIDIL FOR WOMEN
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 FOR WOMEN
- Generic name
- MINOXIDIL
- Manufacturer
- CARDINAL HEALTH 110, LLC. DBA LEADER
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 33f9e0de-dff1-4a14-8aec-8c842bf34c31
- SPL ID
- 33f9e0de-dff1-4a14-8aec-8c842bf34c31
- Version
- 1
- Effective date
- 2026-04-13
- Source export date
- 2026-10-30
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/a3e33fe073aa0aa94eb690c6684c74434c63cebfbf7c5530205a2c3e957ecb8b/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:42:26
| 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 FOR WOMEN | openfda.brand_name | |
| generic name | MINOXIDIL | openfda.generic_name | |
| manufacturer name | CARDINAL HEALTH 110, LLC. DBA LEADER | openfda.manufacturer_name | |
| ndc | package | 70000-0753-1 | openfda.package_ndc |
| ndc | product | 70000-0753 | openfda.product_ndc |
| ndc11 | package | 70000075301 | derived:openfda.package_ndc |
| rxcui | 645146 | openfda.rxcui | |
| spl id | 33f9e0de-dff1-4a14-8aec-8c842bf34c31 | id | |
| spl set id | 33f9e0de-dff1-4a14-8aec-8c842bf34c31 | 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.