warnings
Warnings For external use only. Flammable: Keep away from fire or flame.
Loesch Hair Regrowth Formula Unscented Topical Solution Extra-Strength 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
- Loesch Hair Regrowth Formula Unscented Topical Solution Extra-Strength for Men
- Generic name
- MINOXIDIL
- Manufacturer
- Loesch Laboratory Consultant, INC.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- d158d3af-6850-48c0-8355-9df0637684cc
- SPL ID
- 450fe25c-0ed3-eb99-e063-6394a90a6f32
- Version
- 4
- Effective date
- 2025-12-03
- 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 05:57:17
| 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 | 075598 | derived:openfda.application_number |
| application number | ANDA075598 | openfda.application_number | |
| brand name | Loesch Hair Regrowth Formula Unscented Topical Solution Extra-Strength for Men | openfda.brand_name | |
| generic name | MINOXIDIL | openfda.generic_name | |
| manufacturer name | Loesch Laboratory Consultant, INC. | openfda.manufacturer_name | |
| ndc | package | 25280-006-42 | openfda.package_ndc |
| ndc | product | 25280-006 | openfda.product_ndc |
| ndc11 | package | 25280000642 | derived:openfda.package_ndc |
| rxcui | 311724 | openfda.rxcui | |
| spl id | 450fe25c-0ed3-eb99-e063-6394a90a6f32 | id | |
| spl set id | d158d3af-6850-48c0-8355-9df0637684cc | set_id | |
| unii | 5965120SH1 | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings
Do not use if You are a woman Your amount of hair loss is different than that shown on the side of this carton or your hair loss is on the front of the scalp. Minoxidil Topical Solution 5% is not intended for frontal baldness or receding hairline. You have no family history of hair loss. Your hair loss is sudden and/or patchy. You do not know the reason for your hair loss. You are under 18 years of age. Do not use on babies or children. Your scalp is red, inflamed, infected, irritated, or painful. You use other medicines on the scalp.
warnings
ASK DOCTOR Ask a doctor before use if you have heart disease.
warnings
When using this product Do not apply on other parts of the body. Avoid contact with the eyes. In case of accidental contact, rinse eyes with large amounts of cool tap water. Some people have experienced changes in hair color and/or texture. Results may occur at 2 months with twice daily usage. For some men, you may need to use this product for at least 4 months before you see results. The amount of hair regrowth is different for each person. This product will not work for everyone.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.