Menovazine (Menovasin)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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Dosage form: & nbspsolution for external use [alcohol]
Composition:

Per 100 ml

Active substances:

Levomenthol - 2.5 g.

Procaine hydrochloride (Novocain hydrochloride) 1.0 g.

Benzocaine (anesthesin) - 1.0 g.

Excipient:

Ethanol (ethyl alcohol) 70% - up to 100 ml.

Description:Colorless transparent liquid with a smell of menthol.
Pharmacotherapeutic group:Local anesthetic
ATX: & nbsp
  • Local anesthetics for external use
    • Pharmacodynamics:

    Combination drug for external use. Has a local anesthetic effect.

    Levomenthol when applied to the skin and mucous membranes causes irritation of the nerve endings, expands the surface vessels of the skin, causing a sensation of coolness, accompanied by an analgesic effect and relief of itching. Strengthens the anesthetic effect of procaine and benzocaine.

    Procain - local anesthetic with moderate anesthetic activity. Being a weak base, it blocks Na + - channels, prevents the generation of pulses in the endings of the sensory nerves and impulses along nerve fibers. Changes the action potential in the membranes of nerve cells without a pronounced effect on the resting potential. Suppresses carrying out not only pain, but also impulses of another modality.

    Benzocaine - local anesthetic for superficial anesthesia. Reduces the permeability of the cell membrane for Na +, displaces Ca2+ from receptors located on the inner surface of the membrane, blocks the conduction of nerve impulses. Prevents the appearance of painful impulses in the endings of the sensory nerves and their conduction along nerve fibers.

    Indications:Neuralgia, myalgia, arthralgia and itching dermatoses.
    Contraindications:Hypersensitivity to any of the components of the drug, violation of the integrity of the skin, inflammatory skin diseases at the site of the intended application (including dermatitis, eczema), pregnancy, lactation period, children's age.
    Dosing and Administration:External, apply to the skin over the affected area and rub or on the affected skin areas (itching dermatoses) 2-3 times a day. The course of treatment continues depending on the therapeutic effect, but no more than 3-4 weeks. If necessary, repeat the treatment.
    Side effects:Allergic reactions, contact dermatitis. With prolonged use, dizziness, general weakness, and lowering of blood pressure are possible. In these cases, stop using the drug.
    Special instructions:Data on the effect of the drug on the body during pregnancy and lactation are absent. The efficacy and safety of the drug in patients younger than 18 years of age is not established.
    Form release / dosage:
    Solution for external use alcohol.
    Packaging:

    40 ml or 50 ml in bottles of orange glass.

    Vials with the appropriate number of instructions for medical use are placed in a group container.

    Storage conditions:
    Store in a dark place at a temperature of no higher than 25 ° C. Keep out of the reach of children.
    Shelf life:2 years. Do not use the drug after the expiration date.
    Terms of leave from pharmacies:Without recipe
    Registration number:LSR-003640/10
    Date of registration:30.04.2010
    Expiration Date:Unlimited
    The owner of the registration certificate:KIROVSKAYA PHARMACEUTICAL FACTORY, OJSC KIROVSKAYA PHARMACEUTICAL FACTORY, OJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp29.04.2018
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