Rotokan (Rotocanum)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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Active substanceCalendula officinalis flower extract + Chamomile Pharmaceutical flowers extract + Yarrow ordinary herb extractCalendula officinalis flower extract + Chamomile Pharmaceutical flowers extract + Yarrow ordinary herb extract
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  • Rotokan
    extract locally inwards rect. 
    TULA PHARMACEUTICAL FACTORY, LTD.     Russia
  • Rotokan
    extract locally inwards rect. 
    IVANOVSKAYA Pharmaceutical Factory, OAO     Russia
  • Rotokan
    extract locally inwards rect. 
    BEGRIF, LTD     Russia
  • Rotokan
    extract locally inwards rect. 
    MOSCOW PHARMACEUTICAL FACTORY, CJSC     Russia
  • Rotokan
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    NGO Farmvilar, OOO     Russia
  • Rotokan
    extract locally inwards rect. 
    VLADIVOSTOK FARM FACTORY, OJSC     Russia
  • Rotokan
    extract locally inwards rect. 
    YAROSLAVSK PHARMACEUTICAL FACTORY, CJSC     Russia
  • Rotokan
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    VIFITEH, CJSC     Russia
  • Rotokan
    extract locally inwards rect. 
    PEZ VILAR, SUE     Russia
  • Rotokan
    extract locally inwards rect. 
    KIROVSKAYA PHARMACEUTICAL FACTORY, OJSC     Russia
  • Rotokan
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    ROSTOVSKAYA FARMFABRIKA, CJSC     Russia
  • Rotokan
    extract locally inwards rect. 
    TVERSKAYA PHARMACEUTICAL FACTORY, OJSC     Russia
  • Rotokan
    extract locally inwards rect. 
    VLADIVOSTOK FARM FACTORY, OJSC     Russia
  • Rotokan-VILAR®
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    FARMTSENTR VILAR, ZAO     Russia
    • Dosage form: & nbsp

    Extract for oral and topical use [liquid].

    Composition:

    To prepare 1000 ml of extract it is necessary:

    Active components:

    Chamomile flowers - 500 g

    Nail clippings flowers - 250g

    Yarrow grass - 250 g

    Excipient:

    Ethanol (ethyl alcohol) 40% is sufficient to produce 1000 ml of extract.
    Description:The liquid is dark brown with an orange shade of color with a characteristic smell. During storage, a deposit may occur.
    Pharmacotherapeutic group:Anti-inflammatory agent of plant origin.
    ATX: & nbsp

    A.01.A.B   Antimicrobials for topical use in diseases of the oral cavity

    Pharmacodynamics:

    Has a local anti-inflammatory effect, has haemostatic and antispasmodic properties.

    Indications:

    In stomatology: inflammatory diseases of the mucous membrane of the oral cavity and periodontium of various etiology (aphthous stomatitis, periodontitis, ulcerative necrotic gingivostomatitis).

    In gastroenterology (as part of complex therapy): gastroduodenitis, chronic enteritis and colitis.

    Contraindications:

    Hypersensitivity to the components of the drug, severe renal dysfunction, liver disease, alcoholism, craniocerebral trauma, brain disease, age 18 years.

    Carefully:

    When ingestion - glomerulonephritis, pyelonephritis.

    Pregnancy and lactation:

    Contraindicated use of the drug during pregnancy and during breastfeeding due to the high content of ethanol in the drug.

    Dosing and Administration:

    Inside, topically, rectally. Shake before use.

    In the form of an aqueous solution, which is prepared before use by adding 1 teaspoon of the drug to a glass of warm boiled water. With good tolerability, the dose can be increased to 3 teaspoons per glass of water.

    With diseases of the oral mucosa, the solution of the drug is used by applying (15-20 minutes) or rinsing (1-2 minutes) 2-3 times a day for 2-5 days. Treatment of periodontal diseases is carried out after removal of dental deposits and scraping of pathological gingival pockets.In the gingival pockets injected for 20 minutes, thin turuns, richly moistened with a solution of the drug. The procedure is carried out once a day daily or every other day, only 4-6 times.

    In gastroenterology the drug is used inside and in microclysters (rectally). Inside, apply 1 / 3-1 / 2 cup of water solution 30 minutes before eating or 40-60 minutes after eating 3-4 times a day. The course of treatment is 2-3 weeks.

    Microclysters with 50-100 ml of the aqueous solution of the drug are used after the cleansing enema 1-2 times a day. The course of treatment is 3-6 days.

    Side effects:Allergic reactions are possible.
    Overdose:To date, cases of overdose with the use of the drug has not been recorded. When using the drug inside at doses exceeding the recommended, dizziness, nausea, vomiting are possible. Treatment is symptomatic.
    Interaction:

    Not described.

    Special instructions:The drug contains at least 33% ethanol. When you dilute 1 teaspoon of the drug in a glass of water, the absolute ethyl alcohol content in the maximum single dose is 0.8 g, at a maximum daily dose of 3.2 g. When you dilute 3 teaspoons of the drug in a glass of water, the absolute ethyl alcohol content in the maximum single dose - 2.4 g, in the maximum daily dose - 9.6 g.
    Effect on the ability to drive transp. cf. and fur:When using the drug should refrain from the implementation of potentially hazardous activities requiring increased concentration and speed of psychomotor reactions (driving and other vehicles, working with moving mechanisms).
    Form release / dosage:

    Extract for oral and topical use [liquid].

    To 25, 50, 100 ml in bottles of orange glass with a screw mouth, sealed with polyethylene plugs and screwed plastic caps.

    Each vial with instructions for use is placed in a pack of cardboard.

    Packaging of vials is allowed together with an equal number of instructions for use in group packaging.

    Packaging:

    To 25, 50, 100 ml in bottles of orange glass with a screw mouth, sealed with polyethylene plugs and screwed plastic caps.

    Each vial with instructions for use is placed in a pack of cardboard.

    Packaging of vials is allowed together with an equal number of instructions for use in group packaging.

    Storage conditions:

    In the dark place at a temperature of 15 to 25 ° C.

    Keep out of the reach of children.

    Shelf life:

    2 years.Do not use after the expiration date.

    Terms of leave from pharmacies:Without recipe
    Registration number:LP-001743
    Date of registration:02.07.2012
    The owner of the registration certificate:TULA PHARMACEUTICAL FACTORY, LTD. TULA PHARMACEUTICAL FACTORY, LTD. Russia
    Manufacturer: & nbsp
    Information update date: & nbsp02.07.2012
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