warnings
For external use only. Flamable: Keep away from fire of flame.
REMIXDIL HAIR REGROWTH TREATMENT 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
- REMIXDIL HAIR REGROWTH TREATMENT FOR WOMEN
- Generic name
- MINOXIDIL 2%
- Manufacturer
- Rida LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 0d027e41-8acb-43c0-b9e4-4d3208dc7b37
- SPL ID
- 2efdf23e-eff7-ee51-e063-6394a90ad074
- Version
- 3
- Effective date
- 2025-02-25
- Source export date
- 2026-09-28
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:53:59
| 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 | 078176 | derived:openfda.application_number |
| application number | ANDA078176 | openfda.application_number | |
| brand name | REMIXDIL HAIR REGROWTH TREATMENT FOR WOMEN | openfda.brand_name | |
| generic name | MINOXIDIL 2% | openfda.generic_name | |
| manufacturer name | Rida LLC | openfda.manufacturer_name | |
| ndc | package | 83004-009-01 | openfda.package_ndc |
| ndc | product | 83004-009 | openfda.product_ndc |
| ndc11 | package | 83004000901 | derived:openfda.package_ndc |
| rxcui | 311723 | openfda.rxcui | |
| spl id | 2efdf23e-eff7-ee51-e063-6394a90ad074 | id | |
| spl set id | 0d027e41-8acb-43c0-b9e4-4d3208dc7b37 | 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.