Active substanceIodine + [Potassium iodide + Polyvinyl alcohol]Iodine + [Potassium iodide + Polyvinyl alcohol]
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  • Iodinol
    solution locally externally 
  • Iodinol
    solution locally externally 
  • Iodinol
    solution locally externally 
    SAMARAHEDPROM, JSC     Russia
  • Iodinol
    solution locally externally 
  • Iodinol
    solution locally externally 
  • Iodinol
    solution locally externally 
  • Dosage form: & nbspsolution for local and external use
    Composition:

    Active substance: iodine 1.0 g;

    Excipients: potassium iodide 3.0 g, polyvinyl alcohol 9.0 g, water purified to 1 liter.

    Description:The liquid is dark blue with a characteristic odor, foaming when shaken.
    Pharmacotherapeutic group:Antiseptic
    ATX: & nbsp

    D.08.A.G.03   Iodine

    Pharmacodynamics:

    Iodine-containing 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.Polyvinyl alcohol is a high-molecular compound whose content in iodinol slows the release of iodine and prolongs its interaction with the tissues of the body; reduces also the irritating effect of iodine on the tissue. Iodine has a bactericidal effect on both gram-positive and gram-negative flora (most active on streptococcal flora and Escherichia coli), as well as pathogenic fungi and yeast. A more stable flora is staphylococcus, but with prolonged use of the drug in 80% of cases, staphylococcal flora is suppressed. Pseudomonas aeruginosa is stable. The drug is low toxicity.

    Indications:

    Chronic tonsillitis, purulent otitis, chronic atrophic rhinitis, chronic periodontitis, purulent wounds, trophic and varicose skin ulcers, thermal and chemical burns I-II degree.

    Contraindications:

    Hypersensitivity to the drug components, thyrotoxicosis, herpetiform dermatitis, pregnancy, the period of breastfeeding, perforation of the tympanic membrane.

    Carefully:

    Children under 18 years.

    Dosing and Administration:

    Locally (rinsing, rinsing, lubricating the tonsils); externally (the imposition of gauze wipes).

    With chronic tonsillitis washed lacunae of tonsils and supratonsillar spaces. Produce 4-5 washings at intervals of 2-3 days. Single dose - 50 ml. Do not swallow!

    With purulent otitis: daily instillation of 5-8 drops of iodinol. The course of treatment is 2-4 weeks.

    In the treatment of chronic atrophic rhinitis after preliminary softening and removal of crusts, irrigation of the nasal cavity and pharynx is carried out 2-3 times a week for 2-3 months.

    With chronic periodontitis rinse the mouth 3 times a day for 15 ml after eating.

    With trophic and varicose ulcers put on the surface of the ulcer gauze wipes (in 3 layers), moistened with the drug (pre-wash the skin with warm water and soap, and the skin around the ulcer is smeared with zinc ointment). Dressings are made 1-2 times a day, while the gauze lying on the surface of the ulcer is not removed, but again impregnated with the drug. After 4-7 days, appoint a general or local bath, then again continue this treatment.

    With purulent wounds and infected burns impose a loose gauze dressing impregnated with the drug.

    With fresh thermal and chemical burns I-II extent, also impose a gauze bandage soaked yodinolom, the inner layer of the dressing preparation according to irrigate when needed.

    In the absence of a positive effect within 7 days, you should consult a doctor.

    Side effects:

    Allergic reactions (skin itching).

    With prolonged use - phenomenon "yodizma" in the form of skin rashes, rhinitis, lacrimation, hypersalivation, rhinorrhea, bronhorei, mucosal edema.

    Overdose:

    Symptoms (local and external): The phenomenon of "yodizma" - skin rash, rhinitis, lacrimation, salivation, rhinorrhea, bronhorei, swelling of the mucous membranes.

    Treatment: withdrawal of the drug, symptomatic therapy.

    Symptoms (with accidental ingestion): Salivation, nasal mucosal edema, laryngeal edema, increased sweating, tachycardia, nausea, vomiting, and diarrhea.

    Treatment: gastric lavage first, 1% sodium thiosulfate solution, then with water; symptomatic therapy.

    If you experience any of the above symptoms of an overdose, as well as symptoms not described in the instructions, stop using the drug immediately and consult a doctor.

    Interaction:

    Pharmaceutically incompatible with essential oils, solutions of ammonia, white sedimentary mercury (an explosive mixture is formed).

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

    Special instructions:

    Avoid contact with eyes. If this happens, the eyes should be washed with a large amount of water or 1% solution of sodium thiosulfate,

    Form release / dosage:

    Solution for local and external use.

    Packaging:

    At 25, 40, 50, 60, 70, 80, 100 ml of the preparation into orange-glass bottles with a screw mouth, sealed with polyethylene plugs and screw caps; or ukuporennyh caps are capping-screwed.

    At 25, 40, 50, 60, 70, 80, 100 ml of the preparation in bottles imported brown glass, sealed with polyethylene caps with the control of the first autopsy.

    At 25, 40, 50, 60, 70, 80, 100 ml of the drug into PET bottles, capped with caps with the control of the first opening.

    By 25, 40, 50, 60, 70, 80, 100 ml of the preparation into polymeric bottles, sealed with polymeric nozzles-droppers and caps screwed on.

    For 60, 70, 80, 100 ml of the drug in the bottles-dropper polymer, sealed with polymer stoppers, droppers and caps screwed.

    Each vial, a dropper along with the instruction for use is placed in a pack of cardboard, it is allowed to be equipped with a spray nozzle, additionally placed in a pack.

    The full text of the instructions for use should be applied to the pack.

    It is allowed to pack vials, flasks-droppers without a pack together with an equal number of instructions for use in group packaging (for hospitals).

    By 3, 5, 10 liters of the drug in cans of polyethylene with instructions for use (for hospitals).

    Storage conditions:

    In the dark place 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.

    Terms of leave from pharmacies:On prescription
    Registration number:LP-002971
    Date of registration:23.04.2015
    Expiration Date:23.04.2020
    Date of cancellation:2020-04-23
    The owner of the registration certificate:IVANOVSKAYA Pharmaceutical Factory, OAO IVANOVSKAYA Pharmaceutical Factory, OAO Russia
    Manufacturer: & nbsp
    Representation: & nbspIVANOVSKAYA Pharmaceutical Factory, OAOIVANOVSKAYA Pharmaceutical Factory, OAO
    Information update date: & nbsp28.11.2017
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