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Dosage form: & nbspspray for topical application
Composition:

For one bottle of 20 g or 60 g:

active substance: propolis 1.20 g or 3.60 g;

Excipients: ethyl alcohol 96% (ethanol) 13.80 g or 41.40 g, glycerol distilled (glycerol) 5.00 g or 15.00 g.

Description:

Brown or from a yellow-brown to a reddish brown liquid with a characteristic odor.

Pharmacotherapeutic group:tissue repair stimulator of natural origin
ATX: & nbsp
  • Other antimicrobials
  • Pharmacodynamics:Active substance propolis contains a complex of biologically active natural compounds (flavonoids, amino acids, resins, organic acids, essential oils, vitamins, microelements) and has pronounced antimicrobial, anti-inflammatory, reparative and antioxidant properties.
    Proposol-N is absorbed by the mucous membrane of the oral cavity for 2-4 minutes and shows local therapeutic effect.
    Indications:

    Proposol-N is used topically in the treatment of inflammatory diseases of the oral mucosa: catarrhal gingivitis and stomatitis, aphthous and ulcerative stomatitis, periodontitis.

    Contraindications:

    Hypersensitivity to bee products, age to 18 years.

    Carefully:

    Diseases of the liver, alcoholism, traumatic brain injury, brain diseases, pregnancy, the period of breastfeeding.

    Pregnancy and lactation:

    The use of the drug is possible taking into account the benefits for the mother and the potential risk to the fetus and the baby. It is necessary to consult a doctor.

    Dosing and Administration:

    Locally.

    Prior to use on the aerosol canister, a spray nozzle should be put on, and after that, pressing the nozzle until it stops, irrigate the affected area of ​​the oral mucosa uniformly. Duration of spraying up to 2 seconds. After irrigation, it is advisable not to eat for 15-30 minutes.

    The drug is used 2-6 times a day, and after reducing the inflammatory process - 1-2 times a day until complete recovery. The course of treatment is 7-10 days.

    Side effects:

    Allergic reactions are possible: redness, itching of the skin, angioedema.

    Short-term burning in the place of application.

    Overdose:

    To date, cases of overdose with topical application have not been reported.

    Interaction:Unknown.
    Special instructions:

    In order to avoid blockage of the sprayer opening after the end of the manipulation, it must be purged or placed in a glass with pure water. When using the bottle should be kept strictly upright!

    Avoid contact with eyes.In case of contact with eyes, rinse immediately with plenty of water.

    The concentration of ethanol in the preparation is 70%. The maximum single dose of the drug (0.7 ml) contains 0.4 g of absolute ethyl alcohol, the maximum daily dose (up to 4 ml) - 2.4 g.

    Effect on the ability to drive transp. cf. and fur:

    During the period of application of the drug, one should refrain from carrying out potentially dangerous activities requiring an increased concentration of attention and speed of psychomotor reactions (vehicle management, work with moving mechanisms).

    Form release / dosage:

    Spray for topical application.

    Packaging:

    By 20 g or 60 g in cylinders aerosol monoblock aluminum with an internal phenolic-epoxy protective coating with mechanical dosing pumps, equipped with nozzles throat and safety caps.

    Each balloon with a throat nozzle, safety cap and instructions for use is placed in a pack of cardboard.

    Storage conditions:

    Store at a temperature not exceeding 25 ° C.

    Keep out of the reach of children.

    Protect from direct sunlight.

    Shelf life:

    2 years.

    Do not use after the expiration date.

    Terms of leave from pharmacies:Without recipe
    Registration number:LS-002719
    Date of registration:05.04.2012
    The owner of the registration certificate:MIKROFARM, LLC MIKROFARM, LLC Ukraine
    Manufacturer: & nbsp
    Information update date: & nbsp10.02.2016
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