Mikoderil solution for plank beds. approx. 1% 10ml (bottle-cap.) # 1

Release form, composition and packaging

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Solution for external use is transparent, colorless or slightly yellowish in color, with an ethanol odor.

1 ml

naftifine hydrochloride 10 mg

propylene glycol - 50 mg, ethanol (ethyl alcohol 95%) - 400 mg, purified water - up to 1 ml.

10 ml - dark glass dropper bottle (1) - cardboard packs.

20 ml - dark glass dropper bottle (1) - cardboard packs.

pharmachologic effect

Antifungal, refers to allylamines.

The mechanism of action is associated with inhibition of the biosynthesis of ergosterol, which leads to a violation of the synthesis of the cell wall of the pathogen.

Has a fungicidal effect on dermatophytes, mold fungi, causative agents of sporotrichosis.

It acts fungicidal or fungistatic on yeast fungi, depending on the particular strain.

Possesses antimicrobial activity against various gram-positive and gram-negative microorganisms, which are often combined with fungi.

It has an anti-inflammatory effect, reduces itching.

It is characterized by a prolonged action (up to 24 hours). ''

Indications for use

Onychomycosis, pityriasis versicolor, epidermophytosis of large skin folds and feet, rubromycosis, trichophytosis, microsporia, skin candidiasis, mycoses with secondary bacterial infection.

Contraindications for use

Hypersensitivity to naftifine.

Dosage regimen

Individual, applied externally 1-2 times / day, the duration of treatment varies from 2 weeks to 6 months.

Side effect

In some cases: at the site of application, dryness and redness of the skin, burning sensation.

Application during pregnancy and lactation

Application during pregnancy in recommended doses does not have an adverse effect on the fetus.

Name ENG

MYCODERIL

Clinical and pharmacological group

Antifungal drug for external use

ATX code

Naftifine

Dosage

1% x 10ml

Structure

1 ml - naftifine hydrochloride 10 mg.

Excipients: propylene glycol - 50 mg, ethanol (ethyl alcohol 95%) - 400 mg, purified water - up to 1 ml.

Indications

Onychomycosis, pityriasis versicolor, epidermophytosis of large skin folds and feet, rubromycosis, trichophytosis, microsporia, skin candidiasis, mycoses with secondary bacterial infection.

Storage conditions and periods

At a temperature not higher than 25 degrees.

Expiration date: 3 years

INN / Active ingredient

naftifine hydrochloride

Contraindications

Hypersensitivity to naftifine.

Specifications

Category

Antifungal

Scope of the medicinal product

General

Release form

Solution

Manufacturer country

Russia

Package quantity, pcs

one

Way of introduction

Outwardly

Vacation conditions

Without recipe

Volume, ml.

10 ml

Brand name

OTCPharm

The amount of the dosage form in the primary package

10 ml

Primary packaging type

Dark glass dropper bottle

Type of consumer packaging

Pack of cardboard

Pharmaco-therapeutic group

Antifungal agent

Anatomical and therapeutic characteristics

D01AE22 Naftifine

Dosage form

Solution for external use

Dosage (volume) of the substance in the preparation

1 ml - naftifine hydrochloride 10 mg

Expiration date in days

1095

Package weight, g

40

Mode of application

:

Individually, applied externally 1-2 times / day, the duration of treatment varies from 2 weeks to 6 months.