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

    Camphor racemic (camphor synthetic) - 10 g

    Excipients:

    Petrolatum - 54 grams

    Paraffin oil hard - 8 g

    Lanolin anhydrous - 28 grams

    Description:
    Homogeneous ointment of yellow or yellow-brown 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:
    LS of natural origin, 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 the camphor is unchanged in the form of light and bile.
    Permeability through the blood-brain and placental barrier is high; secretion with mother's milk - high.
    Indications:

    Myalgia, myositis, arthralgia, sciatica, prevention of bedsore formation.

    Contraindications:

    Hypersensitivity, violation of the integrity of the skin or inflammatory skin diseases at the site of the intended application (including dermatitis, eczema); pregnancy, the period of breastfeeding, the age of 18 years (due to lack of data).

    Dosing and Administration:
    Outwardly. A small amount of ointment is applied to the area of ​​pain and light movements are rubbed 2-3 times a day. Prophylaxis for the formation of pressure sores: treatment of the skin 2-3 times a day. After applying the ointment, wash hands thoroughly. The course of treatment is 7-10 days. Conducting repeated courses of treatment is possible on the recommendation of a doctor.
    Side effects:Allergic skin reactions (urticaria); skin irritation; headache, dizziness.
    Overdose:Until now, no cases of overdose with the use of the drug have been reported.
    Interaction:Not found.
    Special instructions:
    Avoid getting the product on open wounds, in the eyes and mucous membranes.
    Effect on the ability to drive transp. cf. and fur:During the treatment period, care must be taken when driving vehicles. And by engaging in other potentially hazardous activities,requiring increased concentration of attention and speed of psychomotor reactions.
    Form release / dosage:
    Ointment for external use 10%.
    Packaging:

    25 g, 50 g in cans of orange glass. 30 g, 40 g in aluminum tubes. 64 (or 49, or 36) cans of 25 g, 50 g with an equal number of instructions for use are placed in a group package of cardboard.

    1 jar, the tube together with the instruction for use is placed in a pack of cardboard.

    1 jar, the tube is placed in a pack of cardboard, on which the full text of instructions for use is printed.

    Storage conditions:
    At a temperature of 12 to 15 ° C, in a place protected from light. Keep out of the reach of children
    Shelf life:
    4 years. Do not use after the expiration date indicated on the package.
    Terms of leave from pharmacies:Without recipe
    Registration number:LP-000781
    Date of registration:03.10.2011
    Expiration Date:Unlimited
    The owner of the registration certificate:TVERSKAYA PHARMACEUTICAL FACTORY, OJSC TVERSKAYA PHARMACEUTICAL FACTORY, OJSC Russia
    Manufacturer: & nbsp
    Representation: & nbspTVERSKAYA PHARMACEUTICAL FACTORY, OJSCTVERSKAYA PHARMACEUTICAL FACTORY, OJSC
    Information update date: & nbsp23.11.2017
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