Ointment Interferon anadrol 50mg hydrogel based on – a drug for external application, representing adsorbed on aluminum hydroxide gel interferon anadrol 50mg derived from genetically modified producer strain. A part of the polyvinyl alcohol ointments, provides the necessary consistency and facilitates film formation on drying of the skin. Ointment – a thick, gel-like, homogeneous mass of white or grayish color during storage may partially delaminate (mix before use).
Part of the interferon anadrol 50mg ointment recombinant alpha-2 has a broad spectrum of antiviral activity (influenza, herpes, etc.), Bacteriostatic and antiinflammatory action and anticancer and immunomodulation activity.
The ointment is used for the treatment of herpetic lesions of the skin and mucous membranes – simple and herpes zoster, recurrent facial herpes, genitals, gingivitis, herpetic stomatitis.
MODE OF APPLICATION
In the treatment of herpetic lesions ointment applied to the affected skin and mucous thin layer 2 times a day with an interval of 12 hours and is dried for 10-15 minutes to form a protective film. The duration of treatment is 3 to 5 days to complete anadrol 50mg disappearance of integrity violations of the skin and mucous membranes.
The drug does not give side effects.
Ointment is contraindicated in persons suffering from allergic diseases in the acute stage.
1 g, 2 g, 3 g or 5 g in glass vials.
The preparation of expired application can not be.
STORAGE AND TRANSPORTATION
In accordance with JV 3.3.2-1248-03.
Store in a dry, dark place at a anadrol 50mg temperature no higher than 10 ° C or below 0 ° C at a relative humidity of 60-80%.
Transportation of all types of anadrol 50mg covered transport at temperature from 0 ° C to 10 ° C.
CONDITIONS OF RELEASE