Active substanceBoric acidBoric acid
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  • Boric Ointment 5%
    ointment externally 
  • Dosage form: & nbspsolution for topical use [alcohol]
    Composition:

    Per 100 ml:

    active substance: boric acid 3 g;

    auxiliary substance: ethanol (ethyl alcohol) 70% to 100 ml.

    Description:

    Colorless transparent liquid with the smell of alcohol.

    Pharmacotherapeutic group:Antiseptic
    ATX: & nbsp

    D.08.A.D   Preparations of boric acid

    Pharmacodynamics:

    Antiseptic; coagulates proteins (including enzymes) of a microbial cell, disrupts the permeability of the cell wall.

    Pharmacokinetics:

    It penetrates well through the skin and mucous membranes; It is slowly excreted and can accumulate in organs and tissues. It is excreted by the kidneys - 50% (within 12 hours), the rest is within 5-7 days.

    Indications:

    Otitis external (acute and chronic) without damaging the tympanic membrane.

    Contraindications:

    Hypersensitivity, chronic renal failure, perforation of the tympanic membrane; pregnancy, child age, lactation.

    Dosing and Administration:

    Locally. With acute and chronic otitis 3-5 drops are applied to the turunda and injected into the external auditory meatus 2-3 times a day. The course of treatment should not exceed 3-5 days.

    Side effects:

    Local reactions: itching, burning, hyperemia of the skin of the external auditory canal.

    Allergic reactions.

    Overdose:

    Symptoms of acute intoxication (with occasional ingestion): nausea, vomiting, diarrhea, gastralgia, dysfunction of the cardiovascular system, stimulation or depression of the central nervous system, hyperpyrexia, erythematous rashes followed by desquamation (possible fatal outcome within 5-7 days), impaired function kidney and liver (including jaundice), circulatory collapse, shock incl. with a lethal outcome.

    Treatment: symptomatic. Blood transfusion, hemo- and peritoneal dialysis.

    Special instructions:

    Avoid contact with mucous membranes.

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

    Does not affect the ability to drive and perform work that requires increased concentration.

    Form release / dosage:Solution for topical application of alcohol, 3%.
    Packaging:

    For 10 ml in bottles of a glass tube for medicines such as FO, corked with polyethylene closures.

    By 10, 25, 40 ml in glass bottles-droppers type FC, PCM, sealed with stoppers-droppers and caps screwed on plastic.

    To 25, 40 ml in glass vials of type FV, sealed with stoppers polyethylene and caps, screwed plastic.

    For 10, 25, 40 ml of the drug in bottles of polyethylene terephthalate.

    Each vial of 10, 25, 40 ml or a dropper of 10, 25, 40 ml together with the appropriate number of instructions for medical use are placed in a group container.

    Storage conditions:

    Store in a dark place at a temperature of 15 to 25 ° C.

    Keep out of the reach of children.

    Shelf life:3 years.
    Do not use the product after the expiration date printed on the package.
    Terms of leave from pharmacies:Without recipe
    Registration number:LSR-006425/10
    Date of registration:06.07.2010
    Expiration Date:Unlimited
    The owner of the registration certificate:KIROVSKAYA PHARMACEUTICAL FACTORY, OJSC KIROVSKAYA PHARMACEUTICAL FACTORY, OJSC Russia
    Manufacturer: & nbsp
    Representation: & nbspKIROVSKAYA PHARMACEUTICAL FACTORY, OJSCKIROVSKAYA PHARMACEUTICAL FACTORY, OJSC
    Information update date: & nbsp19.02.2017
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