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 l.

    Description:

    The liquid is dark blue with a characteristic odor, foaming when shaken. Traces of foaming on the unfilled part of the bottle are allowed.

    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 is stable. The drug is low toxicity.

    Indications:

    Chronic tonsillitis, chronic 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, lactation period, 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 chronic purulent otitis: daily instillation of 5-8 drops of iodinol in mesotympanites and washing of the attic with epitimpanites. A course of treatment - 2-4 of the week.

    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 degree Also impose a gauze dressing impregnated with iodine, the inner layer of the dressings are irrigated with the drug as needed.

    Side effects:

    Allergic reactions (skin itching).

    With prolonged use: the phenomenon of "iodism" in the form of skin eruptions, rhinitis, lacrimation, hypersalivation, rhinorrhea, bronchorrhea, edema of the mucous membranes.

    Overdose:

    Symptoms (local and external): phenomena of "iodism" - skin rashes, rhinitis, lacrimation, hypersalivation, rhinorrhea, bronchorrhea, edema of the mucous membranes.

    Treatment: withdrawal of the drug, symptomatic therapy.

    Symptoms (with accidental ingestion): hypersalivation, edema of the mucous membranes of the nasopharynx, laryngeal edema, increased sweating, tachycardia, nausea, vomiting, diarrhea.

    Treatment: gastric lavage first 1% a solution of sodium thiosulfate, 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:

    To not allow hit preparation in the eye. If this happens, the eyes should be rinsed with plenty of water or 1% solution of sodium thiosulfate.

    Form release / dosage:

    Solution for local and external use.

    Packaging:

    For 40, 50, 80, 100 ml of the drug in orange glass vials with a screw mouth, sealed with polymer caps and polymeric screw caps, or capped with a spray nozzle.

    For 40, 50, 80, 100 ml of the drug in orange glass vials with a screw mouth, sealed with polymeric screw caps.

    For 40, 50, 80, 100 ml of the preparation into glass bottles made of brown and colorless glass, ukuporennye products packaging.

    40, 50, 80, 100 ml into polymeric bottles, sealed with stoppers-droppers or polymeric and polymeric polymer dispensers, or capped with a spray nozzle.

    At 40, 50, 80, 100 ml in bottles of polyethylene terephthalate, sealed with polymer screw caps, or ukuporenny spray nozzle.

    Each vial with the instruction for use is placed in a pack of cardboard, or each vial with instructions for use and a spray nozzle are placed in a pack of cardboard.

    It is allowed to pack bottles in a group package with an equal number of instructions for use.

    For 4.5 liters in a bottle of polyethylene terephthalate (for hospitals).

    Storage conditions:

    In the dark place at a temperature of 5 to 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:On prescription
    Registration number:LP-001828
    Date of registration:10.09.2012
    Date of cancellation:2017-09-10
    The owner of the registration certificate:TULA PHARMACEUTICAL FACTORY, LTD. TULA PHARMACEUTICAL FACTORY, LTD. Russia
    Manufacturer: & nbsp
    Representation: & nbspTULA PHARMACEUTICAL FACTORY, LTD.TULA PHARMACEUTICAL FACTORY, LTD.
    Information update date: & nbsp09.11.2015
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