Composition, form of production and packaging
? Spray for topical application in the form of a transparent or slightly opalescent liquid of red-brown color, unlimitedly miscible with water.
1 ml of 1 fl.
Povidone-iodine 85 mg 2.55 g
allantoin 1 mg 30 mg
Excipients: levomenthol 0.3 g, citric acid monohydrate 0.06 g, sodium citrate dihydrate 0.06 g, ethanol 96% 6 g, propylene glycol 9 g, purified water up to 30 ml.
30 ml - polyethylene bottles (1) with a mechanical spray, a lid and an applicator - packs cardboard.
30 ml - polyethylene bottles (1) with mechanical spray, cover and applicator with swing arm - packs cardboard.
INSTRUCTION FOR THE SPECIALIST.
Description of the drug approved by the manufacturer for the printed edition of 2014.
PHARMACHOLOGIC EFFECT
The drug with an antimicrobial and anti-inflammatory effect for topical use in diseases of the oral cavity and in ENT practice. Upon contact with the skin emits iodine.Has antiseptic and anti-inflammatory effect. Has a wide spectrum of antimicrobial action. It is active against bacteria, viruses, fungi, protozoa.
PHARMACOKINETICS
Data on the pharmacokinetics of the preparation are not provided.
INDICATIONS
- Infectious-inflammatory diseases of the oral cavity and pharynx, incl. tonsillitis, tonsillitis, tonsillopharyngitis, glossitis, stomatitis, aphthae;
- for treatment of the oral cavity and pharynx during surgical interventions on the respiratory tract and oral cavity and in the postoperative period;
- to treat infections of the mouth and throat that occur during chemotherapy;
- when streptococcal angina is used as an additional remedy for antibiotic treatment.
DOSING MODE
The drug is used 2-4 times / day, one injection to the right and left into the oral cavity and pharynx. If necessary, the drug can be used more often, every 4 hours.
Before use, remove the protective cap and install the applicator. Press 2-3 times on the applicator to allow the solution to enter the nebulizer and spray after spraying.After that, place the applicator tube 2-3 cm into the mouth, hold the breath and press 2 times on the cap so that one irrigation was done to the right, and the second - to the left. The applicator is washed with hot water before and after application.
SIDE EFFECT
In some cases: reactions of hypersensitivity to the drug, local manifestations of an allergic reaction to iodine (pruritus, hyperemia), which may require withdrawal of the drug.
With long-term use (more than 7-10 days), the phenomena of iodism (including metallic taste in the mouth, increased salivation, swelling of the eyes, larynx) are possible.
CONTRAINDICATIONS
- dysfunction of the thyroid gland (hyperthyroidism);
- heart failure;
- herpetiform dermatitis of DГјhring;
- simultaneous use of radioactive iodine;
- Children's age till 8 years;
- Pregnancy;
- the period of lactation (breastfeeding);
- hypersensitivity to iodine and other components of the drug.
PREGNANCY AND LACTATION
Contraindicated in pregnancy and lactation (breastfeeding).
APPLICATION FOR CHILDREN
Contraindicated in children under the age of 8 years.
SPECIAL INSTRUCTIONS
The patient should be warned about the need to stop taking the drug and consult a doctor if there are signs of iodism.
The drug is not intended for ingestion, it should not be inhaled or swallowed.
OVERDOSE
Data on the overdose of the preparation of Joeks В® are not provided.
DRUG INTERACTION
It is inappropriate to simultaneously use the preparation Jox В® with other antiseptic agents for topical application in the oral cavity and pharynx, especially containing hydrogen peroxide, due to inactivation of the drug.
TERMS OF RELEASE FROM PHARMACY
The drug is approved for use as a means of OTC.
TERMS AND CONDITIONS OF STORAGE
The drug should be stored out of reach of children, protected from light at a temperature of 10 В° to 25 В° C. Shelf life - 4 years.
