LOMEXIN

This brand name is authorized in Austria, Croatia, Cyprus, Estonia, France, Hong Kong SAR China, Ireland, Lithuania, Mexico, Romania, South Africa, Spain.

Active ingredients

The drug LOMEXIN contains one active pharmaceutical ingredient (API):

1
UNII 8V4JGC8YRF - FENTICONAZOLE NITRATE
 

Fenticonazole is a broad-spectrum antimycotic agent.

 
Read more about Fenticonazole

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 LOMEXIN 2% Cream / Gel / Shampoo / Cutaneous solution / Cutaneous powder MPI, EU: SmPC Web Search

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
D01AC12 Fenticonazole D Dermatologicals → D01 Antifungals for dermatological use → D01A Antifungals for topical use → D01AC Imidazole and triazole derivatives
Discover more medicines within D01AC12
G01AF12 Fenticonazole G Genito urinary system and sex hormones → G01 Gynecological antiinfectives and antiseptics → G01A ANTIINFECTIVES AND ANTISEPTICS, EXCL. COMBINATIONS WITH CORTICOSTEROIDS → G01AF Imidazole derivatives
Discover more medicines within G01AF12

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
EE Ravimiamet 1698802, 1698824, 1698857
ES Centro de información online de medicamentos de la AEMPS 61126, 61128, 61715
FR Base de données publique des médicaments 63987103, 69960586
HK Department of Health Drug Office 60579
HR Agencija za lijekove i medicinske proizvode HR-H-190719220, HR-H-330603769, HR-H-883864037
LT Valstybinė vaistų kontrolės tarnyba 1007529, 1007530, 1007531, 1007532, 1008132, 1008133, 1068927, 1068928, 1079132, 1079133, 1079174, 1079175, 1080816, 1080817
MX Comisión Federal para la Protección contra Riesgos Sanitarios 252M95, 460M96
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W03122001, W03123003, W03123004, W03124002, W03125002, W03125003, W03126002
ZA Health Products Regulatory Authority 29/18.6/0053, 29/18.6/0054, 29/18.6/0055, 32/18.6/0206

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