Active substanceCamphorCamphor
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  • Dosage form: & nbspsolution for external use
    Composition:

    Camphor racemic -100 g.

    Excipient:

    Sunflower oil - up to 1 liter.

    Description:Transparent oily liquid of yellow color with the smell of camphor.
    Pharmacotherapeutic group:Local irritant of natural origin
    ATX: & nbsp

    C.01.E.B   Other drugs for the treatment of heart disease

    C.01.E.B.02   Camphor

    Pharmacodynamics:
    The drug has antiseptic, local irritating, local analgesic and anti-inflammatory effect. Exciting sensitive nerve endings of the skin, dilates the blood vessels and improves the trophism of organs and tissues.
    Pharmacokinetics:When applied to the surface of the skin is partially absorbed, subjected to oxidation. Oxidation products combine with glucuronic acid and are excreted by the kidneys. Part of camphor is excreted unchanged in the form of lungs and bile.
    Indications:
    Arthralgia, myalgia, sciatica, myositis, prophylaxis of decubitus formation.
    Contraindications:
    Hypersensitivity, violation of the integrity of the skin or inflammatory skin diseases at the site of the intended application (incl.dermatitis, eczema), pregnancy, the period of breastfeeding, age to 18 years.
    Dosing and Administration:
    Outwardly. Myalgia, myositis, arthralgia, sciatica: a small amount of oil is applied to the area of ​​pain and rubbing lightly. Apply 2-3 times a day for 7-10 days. Prophylaxis for the formation of pressure sores: treatment of the skin 2-3 times a day.
    Side effects:
    Allergic skin reactions (urticaria), skin irritation, headache, dizziness.
    Overdose:

    Symptoms: agitation, tachycardia, convulsions.

    Treatment: symptomatic.

    Interaction:No data.
    Special instructions:

    Avoid getting the product on open wounds, in the eyes and mucous membranes.

    During the treatment period, care must be taken when driving vehicles and engaging in other potentially hazardous activities requiring increased attention and speed of psychomotor reactions due to the possible side effect of dizziness.

    Effect on the ability to drive transp. cf. and fur:During the treatment period, care must be taken when driving vehicles and engaging in other potentially hazardous activities,requiring increased concentration of attention and speed of psychomotor reactions due to the possible occurrence of a side effect - dizziness.
    Form release / dosage:
    Solution for external use [oil] 10%.
    Packaging:

    To 30, 50 or 100 ml in bottles of orange glass, corked with plastic caps and caps screwed on.

    Each bottle, together with the instructions for use, is placed in a pack of cardboard. Packaging of vials without a pack together with an equal number of instructions for use in group packaging is allowed.

    Storage conditions:
    Store at a temperature not exceeding 25 ° C. Keep out of the reach of children.
    Shelf life:3 years. Do not use after the expiration date printed on the package.
    Terms of leave from pharmacies:Without recipe
    Registration number:PL-000859
    Date of registration:14.10.2011 / 28.09.2017
    Expiration Date:Unlimited
    The owner of the registration certificate:TULA PHARMACEUTICAL FACTORY, LTD. TULA PHARMACEUTICAL FACTORY, LTD. Russia
    Manufacturer: & nbsp
    Representation: & nbspTULA PHARMACEUTICAL FACTORY, LTD.TULA PHARMACEUTICAL FACTORY, LTD.
    Information update date: & nbsp23.11.2017
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