Edermik gel 0.1% tube 30 g

The active substance is dimethindene maleate (1 g of gel contains 1 mg of dimethindene maleate).

Excipients: disodium edetate, carbomer, benzalkonium chloride, propylene glycol, sodium hydroxide 30% solution, purified water.

Increased sensitivity to the components of the drug.

For children under 2 years of age, the drug can be used only as prescribed by a doctor. Babies and young children should not use the drug on large areas of skin, especially on damaged or inflamed skin.

Adults and children over 2 years of age should apply the gel to the affected areas of the skin 2-4 times a day. If the patient’s condition does not improve after 7 days of using the drug, it is necessary to consult a doctor.

In case of very strong itching or damage to a large area, in addition to local application of the drug, oral forms of the drug (“Edermik”, oral drops) should also be used.

pregnant

There are no clinical data on the use of the drug in pregnant women. During pregnancy, it is not recommended to use “Edermik” unless the benefit of use exceeds the potential risk to the fetus. In this case, the drug can only be used as prescribed by a doctor.

It is not recommended to apply “Edermik” to small areas of skin, especially to damaged or inflamed skin. The same applies to women who are breastfeeding. In addition, breastfeeding women should not apply the gel to the nipples of the mammary glands.

Children

For children under 2 years of age, the drug can be used only as prescribed by a doctor. Babies and young children should not use the drug on large areas of skin, especially on damaged or inflamed skin.

Drivers

Dimethindenum maleate when applied externally does not affect the speed of reaction when driving a motor vehicle or working with other mechanisms.

At the moment, there have been no reports of drug overdose.

If you accidentally swallow a large amount of gel, you should immediately consult a doctor.

Some symptoms characteristic of an overdose of H1 _{-antihistamines} for systemic use may be observed: depression of the central nervous system, accompanied by drowsiness (mainly in adults), stimulation of the central nervous system and antimuscarinic effect (especially in children and the elderly), including disorders , ataxia, hallucinations, tonic-clonic convulsions, mydriasis, dry mouth, facial hyperemia, urination disorders, fever, arterial hypotension is also possible.

In case of overdose, it is necessary to take measures recommended by the medical institution in accordance with the symptoms that arise.

The most frequent side effects are minor and short-term skin reactions at the application site. The drug contains benzalkonium chloride and propylene glycol, which can cause skin irritation.

Store in the original packaging at a temperature not higher than 25 °C, in a place inaccessible to children.

Shelf life – 2 years.