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. 
  • Rotokan
    extract locally inwards rect. 
  • Rotokan
    extract locally inwards rect. 
    BEGRIF, LTD     Russia
  • Rotokan
    extract locally inwards rect. 
  • Rotokan
    extract locally inwards rect. 
    NGO Farmvilar, OOO     Russia
  • Rotokan
    extract locally inwards rect. 
  • Rotokan
    extract locally inwards rect. 
  • Rotokan
    extract locally inwards rect. 
    VIFITEH, CJSC     Russia
  • Rotokan
    extract locally inwards rect. 
    PEZ VILAR, SUE     Russia
  • Rotokan
    extract locally inwards rect. 
  • Rotokan
    extract locally inwards rect. 
  • Rotokan
    extract locally inwards rect. 
  • Rotokan
    extract locally inwards rect. 
  • Rotokan-VILAR®
    extract locally inwards rect. 
  • Dosage form: & nbsp

    Extract liquid for oral administration and topical application.

    Composition:

    To obtain 1000 ml of the drug, use:

    Chamomile flowers - 500 g

    Nail clippings flowers - 250g

    Yarrow grass - 250 g

    Excipients:

    Ethyl alcohol (ethanol) 40% - a sufficient amount to obtain 1000 ml of the drug.

    Description:The liquid is dark brown in color with an orange tinge and a specific odor. During storage, precipitation 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: gastroduodenitis, chronic enteritis and colitis (in complex treatment).

    Contraindications:Hypersensitivity to the components of the drug, severe renal dysfunction, liver dysfunction, alcoholism, craniocerebral trauma, brain disease, pregnancy, the period of breastfeeding, age to 18 years.
    Carefully:

    When ingestion - glomerulonephritis, pyelonephritis.

    Dosing and Administration:

    Inside, topically, rectally.

    Rotokan is used 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 in the form of applications (15-20 minutes) or rinses (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 (60-100 ml) 30 minutes before meals or 40-60 minutes after meals, 3-4 times a day. The course of treatment is 2-3 weeks.

    Microclysters of 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 drug overdose have not been reported.

    When using the drug in doses exceeding the recommended, dizziness, nausea, vomiting are possible.

    Measures of help: cancel the drug, symptomatic treatment.

    Interaction:

    Not described.

    Special instructions:The composition contains not less than 33% of ethyl alcohol. In the maximum daily dose of an aqueous solution obtained by adding 1 teaspoon of the preparation to a glass of warm boiled water, the absolute ethyl alcohol content is about 3.2 g. In the maximum daily dose of an aqueous solution obtained by adding 3 teaspoons of the preparation to a glass of warm boiled water , the absolute ethyl alcohol content is about 9.5 g.

    During storage, precipitation may occur.Before use, the contents of the vial should be shaken.
    Effect on the ability to drive transp. cf. and fur:When using the drug inside, you should refrain from engaging in potentially dangerous activities that require an increased concentration of attention and speed of psychomotor reactions (including driving, working with moving mechanisms).
    Form release / dosage:

    Extract liquid for oral administration and topical application.

    To 25 ml, 50 ml in bottles of a dropper of orange glass with a screw mouth. For 25 ml, 50 ml, 90 ml, 100 ml or PO ml in bottles, cans of orange glass with a screw mouth. Each bottle, a dropper, a jar, together with instructions for medical use, is placed in a pack of cardboard. It is allowed to apply the full text of the instruction for medical use on a pack of cardboard.

    Vials, bottles-droppers, banks with an equal number of instructions for medical use put a group container ("for hospitals").

    Packaging:

    To 25 ml, 50 ml in bottles of a dropper of orange glass with a screw mouth. For 25 ml, 50 ml, 90 ml, 100 ml or PO ml in bottles, cans of orange glass with a screw mouth.Each bottle, a dropper, a jar, together with instructions for medical use, is placed in a pack of cardboard. It is allowed to apply the full text of the instruction for medical use on a pack of cardboard.

    Vials, bottles-droppers, banks with an equal number of instructions for medical use put a group container ("for hospitals").

    Storage conditions:

    In the dark place at a temperature of 8 to 25 ° C.

    Keep out of the reach of children.

    Shelf life:

    2 years.

    Do not use after expiry date.

    Terms of leave from pharmacies:Without recipe
    Registration number:LP-002102
    Date of registration:17.06.2013
    The owner of the registration certificate:BEGRIF, LTD BEGRIF, LTD Russia
    Manufacturer: & nbsp
    Information update date: & nbsp25.02.2014
    Illustrated instructions
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