Active substanceSea buckthorn oilSea buckthorn oil
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  • Dosage form: & nbsprectal suppositories
    Composition:

    One suppository contains:

    Active substance:

    Sea buckthorn oil concentrate with carotenoid content of at least 240 mg /% - 0.5 g.

    Basis for the suppository:

    fat solid (vitepsol, supposir) 1.425 g

    glycerol monostearate 0.075 g

    -to obtain a suppository with a mass of 2.0 g.

    Description:Suppositories from orange to dark orange, torpedo-shaped, with a specific odor.
    Pharmacotherapeutic group:Hemorrhoids treatment of plant origin
    ATX: & nbsp

    D.11.A   Other preparations for the treatment of skin diseases

    Pharmacodynamics:Sea buckthorn oil stimulates the reparative processes in the skin and mucous membranes, accelerates the healing of damaged tissues, and has an anti-inflammatory effect. Has antioxidant and cytoprotective action (due to the presence of fat-soluble bioantioxidants reduces the intensity of free radical processes and protects against damage to cellular and subcellular membranes).
    Indications:Hemorrhoids, anal fissures, erosive and ulcerative lesions of the rectum (including erosive ulcerative sphincteritis and proctitis), catarrhal and atrophic proctitis, radiation damage to the mucous membrane of the lower parts of the colon.
    Contraindications:Hypersensitivity to the components of the drug, diarrhea.
    Pregnancy and lactation:The use of the drug during pregnancy and during breastfeeding is possible,if the expected benefit for the mother exceeds the potential risk to the fetus or child. It is necessary to consult a doctor.
    Dosing and Administration:Rectally. After emptying the intestine, the suppository is injected deep into the anus. Adults and adolescents over 14 years of age are prescribed 1 suppository 2 times a day. The duration of treatment is 10-15 days. If necessary, as agreed with the doctor, after 4-6 weeks, the course of treatment is repeated.
    Side effects:Allergic reactions, burning sensation in the anal region, diarrhea are possible.
    Overdose:Cases of overdose are not described.
    Interaction:Not described.
    Effect on the ability to drive transp. cf. and fur:Data on the effect of the drug on the ability to perform potentially hazardous activities requiring increased concentration of attention and speed of psychomotor reactions (vehicle management, work with moving mechanisms) are lacking.
    Form release / dosage:Suppositories rectal 500 mg.
    Packaging:

    For 5 suppositories in a contiguous cell package from a two-layer film or from a film of polymer materials or a PVC / PE film of a white composite or a polyvinyl chloride film.

    Two contour mesh packs, along with instructions for medical use of the drug, are placed in a pack of cardboard.

    Storage conditions:

    In a place protected from moisture and light, at a temperature of 5 to 15 ° 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-003828
    Date of registration:08.09.2016
    Expiration Date:08.09.2021
    The owner of the registration certificate:TULA PHARMACEUTICAL FACTORY, LTD. TULA PHARMACEUTICAL FACTORY, LTD. Russia
    Manufacturer: & nbsp
    Information update date: & nbsp21.05.2017
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