Active substanceChlorhexidineChlorhexidine
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  • Dosage form: & nbspRA mortar for external use [alcohol]
    Composition:Per 1000 ml:

    Active substance:


    Chlorhexidine Bigluconate solution 20%

    (equivalent to 5 g of chlorhexidine bigluconate)

    25 ml (26.625 g)

    Excipients:


    Ethanol (ethyl alcohol 95%)

    - 718.5 ml,

    Purified water

    - up to 1000 ml.

    Description:

    Colorless, transparent or slightly opalescent liquid with a characteristic smell of alcohol.

    Pharmacotherapeutic group:antiseptic
    ATX: & nbsp

    D.08.A.C.02   Chlorhexidine

    G.01.A.X   Other antiseptics and antimicrobials for the treatment of gynecological diseases

    Pharmacodynamics:

    Antiseptic, shows bactericidal action against gram-positive and gram-negative bacteria, has a fungicidal and virucidal effect (against lipophilic viruses). On bacterial spores acts only at elevated temperature.

    Effective against gram-positive and gram-negative bacteria (incl. Treponema spp., Neisseria gonorrhoeae, Chlamydia spp.). viruses and fungi.

    Stable, after treatment of the skin (hands, operating field) is stored on it in a certain amount, sufficient for the manifestation of bactericidal effect.

    Keeps activity (although somewhat reduced) in the presence of blood, pus, various secrets and organic substances.

    Very rarely causes allergic reactions, skin and tissue irritation, does not have a damaging effect on objects made of glass, plastics, metals.

    Indications:

    Hygienic treatment of the hands of medical personnel, the hands of surgeons, for processing the skin of the operating and injection fields, elbows of the donors; disinfection of small surfaces of medical devices,including dental instruments (heat treatment of which is undesirable) in treatment and prevention institutions.

    Hygienic treatment of hands in medical and preventive institutions.

    Hygienic treatment of the hands of medical personnel of institutions of various profiles and purposes.

    Contraindications:

    Hypersensitivity to chlorhexidine and other components of the drug, dermatitis.

    Carefully:

    Childhood.

    Pregnancy and lactation:

    The drug is intended for external use and has practically no systemic effect, however, when used during pregnancy and lactation, attention should be paid to the presence of ethyl alcohol in the formulation.

    Use during pregnancy and breastfeeding is possible if the intended benefit to the mother exceeds the potential risk to the fetus or child.

    Dosing and Administration:

    Outwardly.

    When hygienic treatment of the hands of medical personnel, 5 ml of the drug is applied to the hands and rubbed into the skin for 2 minutes.

    When processing the hands of surgeons before use, the means of the hand are thoroughly washed with warm running water and toilet soap for 2 minutes, dried with a sterile gauze cloth.Then on dry hands, apply the device in portions of 5 ml (at least 2 times) and rub it into the hands, without wiping your hands with a towel.

    When treating the operative field or ulnar folds of donors, the skin is consistently twice wiped with separate sterile gauze tampons, abundantly moistened with the drug. The exposure time after the end of treatment is 2 minutes. On the eve of surgery the patient takes a shower (bath), changes clothes.

    When processing the operating field, the skin is wiped (in one direction) with a sterile swab moistened with the product. Dwell time after processing is 1 minute. For disinfection of small surfaces (tables, equipment, armrests, etc.), surfaces are wiped with a cloth moistened with a cloth. The rate of consumption of the product with this treatment is 100 ml / sq. M.

    Before disinfection from the external surface of medical devices, visible contaminants are removed using tissue wipes moistened with water; internal channels are washed with water using a ruff or syringe with anti-epidemiological measures (rubber gloves, apron).

    Napkins, rinsing water and washing containers are disinfected with boiling or one ofdisinfectants according to the regimens recommended for viral parenteral hepatitis (for tuberculosis - according to the regimens recommended for this infection) according to the current instructive methodological documents. Products after the removal of pollution completely immersed in the solution means, filling them with cavities and channels. The detachable products are immersed in disassembled form.

    Containers with mortar should be tightly closed with lids to avoid evaporation of alcohol and reduce its concentration.

    For disinfection of products previously washed from contamination, the preparation can be used for 3 days repeatedly (provided that the used product is stored in a tightly closed container in order to avoid changing the alcohol concentration).

    When there are first signs of a change in the appearance of the product (the appearance of flakes, haze, etc.), it should be replaced.

    Side effects:

    Allergic reactions (skin rash), dry skin, itching, dermatitis, stickiness of the skin of the hands (within 3-5 minutes), photosensitization.

    If any of the side effects listed in the manual are aggravated, or if you notice any other side effects not listed in the instructions, tell your doctor.

    Overdose:At present, no cases of overdose with external application have been reported.
    Interaction:

    Incompatible with soap, alkalis, and other anionic compounds (colloids, gum arabic, carboxymethyl cellulose).

    Special instructions:

    Do not apply to wounds and mucous membranes.

    In case of contact with the mucous membranes of the eyes, they should be rinsed quickly and thoroughly under running water and dripped with 30% solution of sodium sulfacil (albucid), if necessary, consult a doctor.

    In case of accidental ingestion, immediately rinse the stomach with a large amount of water, then give the adsorbent (10-20 tablets of activated charcoal). If necessary, symptomatic therapy is performed.

    When used externally, ethanol is partially absorbed through the skin and may have a resorptive general toxic effect (central nervous system depression), which should be taken into account when using the drug in children, pregnant women and during lactation.

    The product is easily ignited!

    Avoid contact with open flames and heating devices.

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

    Not studied.

    Form release / dosage:

    Solution for external use [alcohol], 0,5%.

    Packaging:

    For 25 ml, 50 ml and 100 ml in polyethylene bottles complete with a cover with a control opening.

    To 25 ml, 50 ml, 100 ml into polymeric bottles made of polyethylene, sealed with stoppers-droppers polymer and caps screwed with polymer.

    Vials are labeled with labels from label or writing paper or labels from self-adhesive paper.

    Each bottle, together with the instructions for use, is placed in a pack of cardboard.

    For 70 bottles of 25 ml or 70 bottles of 50 ml or 40 bottles of 100 ml packed in film polyethylene shrink or in boxes with partitions or lattices of cardboard together with an equal number of instructions for use (for hospitals).

    Packing from a polyethylene shrink film or on a cardboard box is labeled with label paper or writing paper or labels from self-adhesive paper.

    500 ml, 1000 ml in polymeric bottles made of polyethylene, sealed with polymer caps and caps with screwable polymer (for hospitals).

    Vials are labeled with labels from label or writing paper or labels from self-adhesive paper.

    For 12 bottles of 500 ml or 8 bottles of 1000 ml each, they are packed in film with a polyethylene shrink or in boxes with septums or cardboard gratings together with an equal number of instructions for use (for hospitals).

    Packing from a polyethylene shrink film or on a cardboard box is labeled with label paper or writing paper or labels from self-adhesive paper.

    For 3 kg, 5 kg, 10 kg, 20 kg in polyethylene cans made of polyethylene (for hospitals). The canister is labeled.

    Four canisters together with an equal number of instructions for use are wrapped in a polyethylene shrink film (for hospitals).

    Packing of polyethylene shrink film is glued with labels from label or writing paper or labels from self-adhesive paper.

    Storage conditions:

    In the dark place, in a well-ukuporennoy container, away from the fire, at a temperature of 2 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:LP-003949
    Date of registration:09.11.2016
    Expiration Date:09.11.2021
    The owner of the registration certificate:Farmanova, Open CompanyFarmanova, Open Company Russia
    Manufacturer: & nbsp
    Representation: & nbspBioFarmKombinat, Open CompanyBioFarmKombinat, Open CompanyRussia
    Information update date: & nbsp10.12.2016
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