Active substanceAllantoin + Povidone-IodineAllantoin + Povidone-Iodine
Similar drugsTo uncover
Dosage form: & nbsptopical solution
Composition:

Active substances (50 ml / 100 ml):

Povidone-iodine 4.250 g / 8.500 g, allantoin 0.050 g / 0.100 g

Auxiliary substances (50 ml / 100 ml):

Levometol 0.500 / 1.000 g, citric acid monohydrate acid 0.100 / 0.200 g, sodium citrate dihydrate 0.100 / 0.200 g, ethanol 96% 10,000 / 20,000 g, propylene glycol 15,000 / 30,000 g, purified water up to 50,000 / 100,000 ml.

Description:

Transparent or slightly opalescent liquid of red-brown color, unlimitedly miscible with water.

Pharmacotherapeutic group:Antiseptic
ATX: & nbsp

R.02.A.A.15   Povidone-iodine

A.01.A.D   Other preparations for topical use in diseases of the oral cavity

Pharmacodynamics:

Combination drug for topical use in diseases of the oral cavity and ENT organs. In contact with skin or mucous membranes, iodine; has antiseptic and anti-inflammatory effect.

The drug has a wide range of antimicrobial effects.

It is active against bacteria, fungi, viruses, protozoa.

Indications:

1. Infectious-inflammatory diseases of the oral cavity and pharynx: including tonsillitis, tonsillitis, tonsilopharyngitis, glossitis, stomatitis, aphthae;

2.For treatment of the oral cavity and pharynx with surgical interventions on the respiratory tract and oral cavity and in the postoperative period;

3. To treat infections of the mouth and throat that occur during chemotherapy;

4. When streptococcal angina is used as an additional remedy for antibiotic treatment.

Contraindications:

- Hypersensitivity to iodine and other components of the drug;

- pregnancy and the period of breastfeeding;

- children under 6 years;

- dysfunction of the thyroid gland (hyperthyroidism);

- heart failure;

- herpetiform dermatitis of Dühring;

- simultaneous use of radioactive iodine.

Dosing and Administration:

Locally.

The solution of the preparation should be diluted with water in a ratio of 1: 20-1: 40 (ie from 2.5 ml to 5 ml using a measuring cup enclosed in the package or ½ -1 teaspoon in 100 ml of water).

Dilute the mouth and throat with a diluted solution. Use a preparation of Yoks-Teva solution is recommended 2-4 times a day, if necessary, the drug can be used more often, up to 6 times a day.

Minimum intervals between rinses - 4 hours.

Side effects:

The preparation of Jox®-Teva solution is usually well tolerated.

In some cases, there may be reactions of hypersensitivity to the drug and the manifestation of an allergic reaction to iodine (itching, congestion), which requires the withdrawal of the drug.

Prolonged use of the drug may cause a phenomenon of iodism (including: metallic taste, excessive salivation, swelling of the eyes or larynx), when it appears, stop using the drug and consult a doctor.

Interaction:

It is not recommended simultaneous use of the preparation Jox®-Teva with other antiseptic agents intended for topical administration in the oral cavity and pharynx, especially containing hydrogen peroxide, due to inactivation of the drug.

Special instructions:

Not intended for oral administration.

Do not inhale or swallow the drug.

The preparation contains about 19% ethanol.

Form release / dosage:

Solution for topical application.

Packaging:

To 50 and 100 ml in bottles of dark glass with a screwed-on propylene lid with the control of the first opening and a measuring cap. Each vial with instructions for use is placed in a cardboard box.

Storage conditions:

At a temperature of 10 ° C to 25 ° C in a dark place.

Keep out of the reach of children.

Shelf life:3 years.

Do not use after the expiry date printed on the package!

Terms of leave from pharmacies:Without recipe
Registration number:П N014300 / 01
Date of registration:04.09.2008 / 30.04.2014
Expiration Date:Unlimited
The owner of the registration certificate:АЙВЭКС Фармасьютикалс с.р.о.АЙВЭКС Фармасьютикалс с.р.о. Czech Republic
Manufacturer: & nbsp
Representation: & nbspTeva Teva Israel
Information update date: & nbsp29.11.2017
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