What you need to know before taking Oksalin Junior
Do not use Oxalin Junior
If you are allergic to oxymetazoline hydrochloride or any of the other ingredients of this medicine.
If you have dry rhinitis (atrophic rhinitis with scabs).
Warnings and Precautions
Talk to your doctor, pharmacist or nurse before using Oxalin Junior.
Oksalin Junior can be used with extreme caution and only after consulting a doctor in case of:
treatment with monoamine oxidase inhibitors (MAOIs) and other drugs that increase blood pressure;
increased pressure in the eyes, especially with the so-called angle-closure glaucoma;
severe diseases of the heart and blood vessels, for example, coronary heart disease, arterial hypertension;
pheochromocytoma (a tumor in the glands just above the kidneys);
overactive thyroid gland, diabetes mellitus.
Oxalin Junior should not be used for more than 3-5 days and at doses higher than recommended, as this can lead to a decrease in the effect of the drug and cause difficult-to-heal changes in the nasal mucosa.
Children and youth
Oksalin Junior is intended for children over 6 years of age.
Do not use the drug in infants and children under 6 years of age.
Other drugs and Oksalin Junior
Tell the doctor or pharmacist about all medications the patient is currently or recently taking, and any medications the patient plans to take. Overdose or accidental use of the drug, as well as the use of tricyclic antidepressants or monoamine oxidase inhibitors (drugs used, for example, for depression), simultaneously or immediately before taking oxymetazoline, can increase blood pressure.
Pregnancy and lactation
If you are pregnant or breastfeeding, suspect you are pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
Driving vehicles and operating machinery
It is impossible to exclude a systemic effect on the cardiovascular system with prolonged use of the drug or use at higher doses than recommended. In such cases, psychophysical preparedness, the ability to drive vehicles and work with mechanisms may be impaired.
Oxalin Junior contains benzalkonium chloride.
The drug contains 0.1 mg of benzalkonium chloride in each g of gel. Benzalkonium chloride may cause irritation or swelling inside the nose, especially with prolonged use.
Package contents and other information
What Oksalin Junior contains
The active substance is oxymetazoline hydrochloride. 1 g of gel contains 0.5 mg of oxymetazoline hydrochloride.
Other Ingredients: Sodium Chloride; disodium phosphate dodecahydrate; sodium dihydrogen phosphate monohydrate; edetate disodium; hydroxyethylcellulose; glycerol; benzalkonium chloride solution; Purified water.
What Oksalin Junior looks like and contents of the pack
Oxalin Junior is available as a colorless or light yellow, clear or slightly opalescent thick liquid.
The drug is available:
in glass bottles with a sprayer, containing 10 g of gel, in a cardboard pack,
in polyethylene bottles of 15 ml, sealed with a dosing pump and an applicator with a protective cap, containing 10 g of gel, in a cardboard pack.
Marketing authorization holder and manufacturer
Responsible person
Warszawskie Zakłady Farmaceutyczne Polfa SA
st. Karolkova 22/24, 01-207 Warsaw
Manufacturer
Warszawskie Zakłady Farmaceutyczne Polfa SA
st. Karolkova 22/24,
01-207 Warsaw
POLPHARMA SA Pharmaceutical plant
Medan branch in Sieradz
st. Vladislav Loketek 10
98-200 Sieradz
For more information please contact your local
Responsible Representative:
Warszawskie Zakłady Farmaceutyczne Polfa SA
st. Karolkova 22/24,
01-207 Warsaw
phone: 22 691 39 00
Oksalyn Junior. Composition and form of release: 1 g of nasal gel contains 0.5 mg of oxymetazoline hydrochloride. 1 dose of gel with a volume of 0.1 ml contains 0.05 mg of oxymetazoline hydrochloride. Excipients with known effect: benzalkonium chloride 0.1 mg/g. Indications: Edema of the mucous membranes that occurs in: acute rhinitis; vasomotor rhinitis; allergic rhinitis; inflammation of the paranasal sinuses; syringitis; otitis media. Contraindications: Hypersensitivity to any component of the drug. Dry rhinitis. Responsible person: Polfa Warszawa SA SmPC: 2020.07.28.
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