Strepsils® plus (Strepsils® Plus)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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Dosage form: & nbsplozenges
Composition:

One tablet for resorption contains:

active substances: 2,4-dichlorobenzyl alcohol 1.2 mg, amylmetacresol 0.6 mg, lidocaine hydrochloride monohydrate 10 mg;

Excipients: wine acid 26 mg, sodium saccharinate 2.08 mg, levomentol 2.08 mg, peppermint mint oil 2.08 mg, seed anise seed 0.52 mg, quinoline yellow color 0.0046 mg, indigo carmine 0.0156 mg, sucrose liquid 1523.4 mg, dextrose liquid [dextrose, oligo- and polysaccharides] 980.9 mg.

Description:

Ploskotsilindricheskie tablets bluish-green color with a letter S from 2 sides of a tablet, with a smell of menthol. Allowed the presence of white deposits, minor air bubbles inside the caramel mass and uneven edges.

Pharmacotherapeutic group:antiseptic
ATX: & nbsp
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    • Pharmacodynamics:

    The drug has an antiseptic effect, is active against gram-positive and gram-negative microorganisms, has antimycotic action. It also has local anesthetic and anti-edematous action.

    Indications:

    Symptomatic treatment of pain in the oral cavity, throat, larynx with infectious inflammatory diseases: tonsillitis, pharyngitis, laryngitis (incl.professional character - from teachers, speakers, workers in the chemical and coal industries), hoarseness, inflammation of the mucous membrane of the mouth and gums (aphthous stomatitis, gingivitis, thrush).

    Contraindications:

    - Hypersensitivity to the components of the drug;

    - children's age (up to 12 years).

    Carefully:Pregnancy, lactation.
    Pregnancy and lactation:

    The use of the drug during pregnancy and lactation is possible only under the supervision of a doctor.

    Dosing and Administration:

    Locally.

    Adults and children over 12 years of age - every 2-3 hours, dissolve 1 tablet.

    Do not use more than 8 tablets within 24 hours.

    Duration of application - no more than 5 days.

    Side effects:

    Allergic reactions, loss of sensitivity of the tongue.

    Overdose:

    It is unlikely that a possible overdose may lead to anesthesia of the upper digestive tract.

    Treatment: symptomatic.

    Interaction:

    Clinically significant interactions with other drugs have not been reported.

    Special instructions:

    If there is a possible loss in the sensitivity of the tongue, we recommend caution when taking hot food and water.

    Do not use the drug in the presence of increased individual sensitivity to any component that is part of the drug.

    When appointing patients with diabetes should take into account that 1 tablet contains 2.6 grams of sugar.

    Form release / dosage:Lozenges.
    Packaging:

    For 4, 6, 8 or 12 tablets in a blister of PVC / PVDC / aluminum.

    For 1, 2 or 3 blisters are put in a cardboard box, or in a metal box, or in a package of packaging laminated foil, or attached to a cardboard cover along with instructions for use.

    Storage conditions:

    In a dry place, at a temperature of no higher than 25 ° C.

    Keep out of the reach of children.

    Shelf life:

    3 years.

    Do not use the drug with expired shelf life.

    Terms of leave from pharmacies:Without recipe
    Registration number:П N014746 / 01
    Date of registration:04.12.2008
    The owner of the registration certificate:Rekitt Benckiser Helsar International Ltd.Rekitt Benckiser Helsar International Ltd. United Kingdom
    Manufacturer: & nbsp
    Representation: & nbspREKITT BENKIZER HELSKER LTD. REKITT BENKIZER HELSKER LTD. United Kingdom
    Information update date: & nbsp20.03.2016
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