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PRODUCT DETAIL

Minoxidil mioWell 20 mg/ml dermálny roztok

Code 0114F
MA number 46/0195/25-S
Product Form: sol der 1x100 ml (fľ.PET)
MA Status: R - Valid Marketing Authorisation
Type of procedure: Decentralised
MAH, country: mioWell s.r.o., Slovakia
Therapeutic Class: 46 - DERMATOLOGICA
ATC:
D DERMATOLOGICALS
D11 OTHER DERMATOLOGICAL PREPARATIONS
D11A OTHER DERMATOLOGICAL PREPARATIONS
D11AX Other dermatologicals
D11AX01 Minoxidil for local use
Shelf life: 48
Container: bottle polyethylene terephtalate (PET)
Route of admin.: Cutaneous use
Prescription Status: Medicinal product not subject to medical prescription.
Legal basis: Article 10(3) hybrid application
MA issued: 29.05.2025
Validity: 29.05.2030
Pediatric warnings: Yes
SPC: SPC_Minoxidil mioWell 20 mg/ml dermálny roztok_sol der_05/2025_REG.pdf  
PIL: PIL_Minoxidil mioWell 20 mg/ml dermálny roztok_sol der_05/2025_REG.pdf  
Safety feature No
Data update: 20.06.2025
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