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MEXIDOL® (Emoxipine) 125 mg, 50 coated tablets
$17.00
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ARPEFLU (Umifenovir) 100 mg, 20/30 caps
$24.00 – $33.00
Description
The instruction for medical use of Dekseril® medicine the Trade name of Dekseril® the International unlicensed name Is not present the Dosage form external use Cream Structure 100 g of drug contain: active agents: glycerin of 15 g, paraffin of white soft 8 g, liquid paraffin of 2 g, excipients: stearic acid, glycerin monostearate, polydimethylcyclosiloxane, dimetikon, a macrogoal 600, trolamin, parahydroxybenzoate, water purified spent on drink. Description Smooth white cream Pharmacotherapeutic group of Dermatoprotektora. Paraffin and fats drugs. The ATX D02AC code the Pharmacological Drug Dekseril® properties possesses the softening action at excessive xeroderma. Indications – auxiliary treatment of xeroderma at certain types of a dermatosis, such as atopic dermatitis, ichthyosis and psoriasis – auxiliary therapy of the superficial burns affecting the small area of an integument the Route of administration and doses It is intended for external use. A thin film of cream is applied on affected areas of skin 1-2 times a day or is more often if it is necessary. Side effects – skin allergic reactions of the Contraindication – hypersensitivity to any component of drug Medicinal interactions of the Research on interaction with other medicines were not carried out. Special instructions In view of existence in composition of drug of the propilparagidroksibenzoat are possible single a case skin allergic reactions, such as eczema or, in some cases, development of a small tortoiseshell is possible. Pregnancy and the period of a lactation of Dekseril® can be used at pregnant women as system influence of active components of drug is insignificant. Дексерил® it is possible to use in the period of a lactation, but use of drug on breast skin during feeding is not recommended by a breast. Features of influence of medicine on ability to run the vehicle or potentially dangerous mechanisms the Overdose About cases of overdose does not influence it was not reported. The form of release and packing of 50 g or 250 g of drug place in the white low-density polyethylene tubas closed by a white polypropylene cap. 1 tuba together with the instruction for medical use in the state and Russian languages is placed in a pack from cardboard. To Store storage conditions at a temperature not above 25 °C. To store out of children’s reach! 3 years not to apply a period of storage after the termination of the expiration date specified on packing. Prescription status Without prescription of Proizvoditel Pierre Fabr Medikament Production, Etablissement Progipharm – Rue du Lycée – 45500 GIEN, France the Owner of the registration certificate of Pierre Fabr Medikament Production, France the Address of the organization accepting in the territory of the Republic of Kazakhstan claims from consumers on quality of products (goods): VIVA FARM LLP Kazakhstan, 050030, Almaty 2nd Ostroumova St., 33
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