NIOTITE-DF

ear drops, 10 ml

Dispensing conditions: NO PRESCRIPTION 

THERAPEUTIC INDICATIONS:

  • external otitis media without perforation of the eardrum;

  • non-purulent otitis media.

dwldDownload instructions for use

Composition

10 ml of the product contains:

  • active substance: chloramphenicol 0.1 g, lidocaine hydrochloride 0.1 g;
  • excipients: boric acid 0.1 g, ethyl alcohol 70%.

Pharmaceutical form

Ear drops, 10 ml.

Pharmacotherapeutic group

Sense organsMedications for otological diseases. Other medications for otological diseases. Analgesics and anesthetics. Combination drugs.

ATC code S02DA30

Indications

  • external otitis media without perforation of the eardrum;
  • non-purulent otitis media.

Contraindications

  • perforation of the eardrum of infectious or traumatic nature;
  • individual hypersensitivity to any component of the product;
  • pregnancy and lactation period;
  • children under 3 years of age;
  • viral or fungal ear diseases;
  • eczema of the external auditory canal;
  • suppression of bone marrow hematopoiesis;
  • acute intermittent porphyria;
  • glucose-6-phosphate dehydrogenase deficiency.

Posology and method of administration

In the external auditory canal instill 2-3 times a day:

  • for children over 3 years of age 2-3 drops;
  • for adults and children over 14 years of age 3-4 drops

Course of treatment: for children - 2-5 days; for adults - 5-7 days.

Adverse reactions

Rare:

  • irritation of skin and mucous membranes;
  • local allergic reactions in the form of rash, itching, redness and swelling of tissues.

Overdose

No overdose has been observed with topical application.

Symptoms of accidental ingestion: nausea, vomiting, diarrhea, headache, skin rashes, confusion, low body temperature.

Treatment: symptomatic, it is necessary to ensure sufficient fluid intake into the body.

Use during pregnancy or breastfeeding

Contraindicated.

Pediatric population

For children, use only when prescribed by your doctor.

Special warnings

The doctor should check the integrity of the eardrum before prescribing treatment.

The product should not be prescribed for prophylactic purposes.

Do not exceed the prescribed course of treatment and doses. If you increase the frequency or duration of product administration, the systemic effect of the active ingredients is possible. Lidocaine may cause neuro- and cardiotoxic reactions-paresthesias, dizziness, drowsiness, agitation, fasciculations, tremors; tachycardia and hypertension. 

Presentation and package

10 ml of the product in glass bottles, sealed with a screw-on plastic cap, complete with a screw-on plastic cap, combining a glass dropper and a rubber nipple. One bottle with a screw cap combining a glass dropper and a rubber nipple, together with instructions for use in the Kazakh and Russian languages are placed in a carton pack.

Storage conditions

Store in a place protected from light, at a temperature below 200С.

Keep out of the reach of children.

Shelf life

3 years

After opening the bottle, the period of using the product is 15 days.

Manufacturer

"DOSFARM" LLP, 3 Chaplygin street, Almaty city, 050034, Kazakhstan, tel.: (727) 253-03-88.

Marketing authorization holder

"DOSFARM" LLP, 3 Chaplygin street, Almaty city, 050034, Kazakhstan.

Name, address, contact information of the organization accepting claims (proposals) against quality of products from consumers in the territory of the Republic of Kazakhstan, which is responsible for post-authorization safety surveillance of the medicine:

"DOSFARM" LLP, 3 Chaplygin street, Almaty city, 050034, Kazakhstan,

Tel./Fax: (727) 253-07-07, 253-03-88, e-mail: Этот адрес электронной почты защищён от спам-ботов. У вас должен быть включен JavaScript для просмотра.

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