Compound
1 g of solution contains: Active ingredients: lidocaine hydrochloride 10 mg, phenazone 40 mg; Excipients: sodium thiosulfate 1 mg, ethanol 221.8 mg, glycerol 709 mg, water 18.2 mg.

Indications
Local symptomatic treatment and pain relief in children from birth and adults with otitis media with an intact eardrum, including:
acute exudative otitis media;
otitis as a complication after influenza, exudative viral otitis;
barotraumatic otitis.

Use during pregnancy and breastfeeding
If the eardrum is intact and the drug is used correctly, the likelihood of active substances entering the systemic circulation is extremely low. In this regard, in the absence of contraindications, the use of Otipax® by pregnant women and women during breastfeeding is possible.

Contraindications
Hypersensitivity to the components of the drug;
Perforation of the eardrum (including those of infectious or traumatic origin)

Carefully
It is necessary to ensure the integrity of the eardrum before starting to use the drug. If the drug is used with a perforated eardrum, the drug may come into contact with the organs of the middle ear and lead to complications.

Side effects
There is a risk of local allergic reactions, irritation and hyperemia of the ear canal. Please notify your doctor of all cases of undesirable reactions not listed in the instructions.

How to take, course of administration and dosage
Otipax® is used in children from birth and adults topically, by instilling 4 drops into the external auditory canal on the affected side 2-3 times a day. To avoid contact of the cold solution with the auricle, the bottle should be warmed in the palms before use. The duration of treatment with Otipax® is no more than 10 days, after which the prescribed treatment should be reconsidered.

Storage conditions
At a temperature not higher than 30C.
Keep out of the reach of children!

Best before date
3 years.
After opening the bottle, the drug should be used within 1 month. Do not use after the expiration date stated on the packaging.