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

    Active substance: boric acid - 3 g;

    Excipients: Ethanol (rectified ethyl alcohol from food raw materials) - 64.27 g, purified water to 100.0 g.

    Description:Transparent colorless liquid with a characteristic odor.
    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 for 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, lactation, children under 18 years.

    Pregnancy and lactation:

    Contraindicated.

    Dosing and Administration:

    Locally.

    With acute and chronic otitis 3 to 5 drops are applied: on turundum and injected at external auditory meatus 2-3 times a day. The course of treatment should not exceed 3-5 days.

    If there is no improvement after treatment, or the symptoms worsen, or new symptoms appear, it is necessary to consult a doctor.Use the drug only according to the indications, the method of administration and the doses specified in the instructions for use.
    Side effects:

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

    Allergic reactions.

    If any of the side effects listed in the manual are aggravated, or any other side effects not indicated in the instructions are noted, the doctor should be informed immediately.

    Overdose:

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

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

    Interaction:

    Not studied.

    Special instructions:

    Avoid contact with mucous membranes.

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

    Does not affect the ability to drive vehicles, mechanisms.

    Form release / dosage:

    Solution for topical application [alcohol] 3%.

    Packaging:

    25 ml glass vials with screw neck orange glass, polymer and rubber stoppers screw-capped polymer.

    For 96 Vials with an equal number of instructions for use are placed in a corrugated cardboard box (for hospitals or pharmacies production departments).
    Storage conditions:

    AT protected from light at a temperature of no higher than 25 ° C. Keep out of the reach of children.

    Shelf life:

    3 years. Do not use after the expiration date printed on the package.

    Terms of leave from pharmacies:For hospitals
    Registration number:LP-004538
    Date of registration:14.11.2017
    Expiration Date:14.11.2022
    The owner of the registration certificate:ARMAVIR DISTRICT PHARMACEUTICAL BASE, OJSC ARMAVIR DISTRICT PHARMACEUTICAL BASE, OJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp07.12.2017
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