Active substanceIodine + [Potassium iodide + Ethanol]Iodine + [Potassium iodide + Ethanol]
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  • Dosage form: & nbspsolution for external use [alcohol]
    Composition:

    Iodine, or iodine of a small-crystalline instantly soluble in 100% ist. 5 g; potassium iodide 2 g, purified water and ethyl alcohol (ethanol) 95% in half to 100 ml.

    Description:Transparent liquid of red-brown color with a characteristic smell.
    Pharmacotherapeutic group:Antiseptic
    ATX: & nbsp

    D.08.A.G.03   Iodine

    Pharmacodynamics:

    Antiseptic. The main active substance is molecular iodine, which has an antiseptic property. When applied to large areas of the skin iodine has a resorptive effect: actively affects the metabolism, enhances the processes of dissimilation, participates in the synthesis of thyroxine, has a proteolytic effect. Ethyl alcohol slows the excretion of iodine and reduces its irritating effect on the tissue.

    It has a bactericidal effect on both gram-positive and gram-negative flora (most active in streptococcal flora and Escherichia coli), as well as pathogenic fungi and yeast. A more stable flora is staphylococcus,However, with prolonged use of the drug in 80% of cases, it disappears. Pseudomonas aeruginosa is stable. The drug is low toxicity.

    Pharmacokinetics:

    Upon contact with the skin, it is converted into iodides by 30%, and the rest into active iodine. Partially absorbed. The absorbed part penetrates into tissues and organs, is selectively absorbed by the thyroid gland. It is allocated by kidneys (mainly), intestines, sweat and mammary glands.

    Indications:

    Inflammatory and infectious diseases of the skin, abrasions, cuts, microtrauma, wounds; myositis, neuralgia, inflammatory infiltrates; disinfection of the operating field (pre- and postoperative treatment of the operating field, injection, puncture, catheterization), wound edges, surgeon's fingers.

    Contraindications:

    Hypersensitivity, thyrotoxicosis, herpetiform dermatitis.

    Pregnancy and lactation:Application in accordance with the instructions is possible.
    Dosing and Administration:

    Oternally, the affected areas of the skin are lubricated. When treating the surgical field, the skin is wiped twice with a sterile gauze pad moistened in solution. The total processing time is 4-6 minutes.

    Side effects:

    With external application: skin irritation, allergic reactions (skin itching), with prolonged use on extensive wound surfaces - iodism (rhinitis, urticaria, Quincke's edema, excessive salivation, lacrimation, acne).

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

    Interaction:

    PharmaceuticallyIt is compatible with essential oils, ammonia solutions, white sedimentary mercury (an explosive mixture is formed).

    Special instructions:

    Light and temperature above 40 ° C accelerate the decay of active iodine. The drug should have a dark brown color. Discoloration of the solution indicates the destruction of the complex with the transition of active iodine to iodide ion and a decrease in the effectiveness of the preparation.

    Alkaline or acidic medium, the presence of fat, pus, blood weaken antiseptic activity.

    Avoid contact with eyes.

    Effect on the ability to drive transp. cf. and fur:The use of the drug according to the instructions for medical use does not adversely affect the performance of potentially hazardous activities requiring special attention and speed of response.
    Form release / dosage:Solution for external use [alcoholic], 5%.
    Packaging:

    By 10, 15, 25, 50, 100, 500, 1000 ml into bottles of glass with a screw mouth, sealed with polyethylene plugs and caps screwed on plastic.

    For 10 ml in glass bottles with a screw neck with closures for alcohol solution of iodine and ammonia solution.

    For 10 ml in glass bottles with a screw neck, sealed with polyethylene threaded caps with sealing element and pomat.

    10, 15, 25, 50, 100, 250, 500, 1000, 1500, 2000, 4500, 5000 ml into the bottles of polyethylene terephthalate, sealed with screwed polyethylene caps with perforations.

    To 100 ml in bottles of glass with a screw mouth, sealed with lids with stoppers.

    For 15, 25 ml in bottles of glass with a dropper, ukuporennyh stoppers.

    For 9 kg and 18 kg in a glass bottle with a screw neck, sealed with screwed plastic covers with gaskets.

    48 kg per barrel polyethylene with screw caps.

    Bottles of polyethylene terephthalate from 10 to 2000 ml are packed in a film polyethylene shrink. Vials of glass from 10 to 1000 ml and bottles of polyethylene terephthalate from 10 to 5000 ml are placed in a box with partitions or lattices of cardboard box or corrugated box.

    Vials of glass from 10 to 50 ml and bottles of polyethylene terephthalate from 10 to 50 ml are stacked in stacks of wrapping paper and pasted with a wrapper of wrapping paper.

    In the shrink film, boxes, packets of group packaging from 10 to 100 ml, intended for delivery to the pharmacy network, the number of instructions for medical use is equal to the number of primary packages.

    On bottles, bottles, barrels paste labels from paper label, writing.

    Storage conditions:

    In a place protected from light, out of reach of children, 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 date shown on the package.

    Terms of leave from pharmacies:Without recipe
    Registration number:LS-000364
    Date of registration:25.06.2010 / 24.11.2016
    Expiration Date:Unlimited
    The owner of the registration certificate:TROITSKY IODNY FACTORY, OJSC TROITSKY IODNY FACTORY, OJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp17.11.2017
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