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MISTININ-DF

eye drops 0.01%, 5 ml and 10 ml

Dispensing conditions: PRESCRIPTION ONLY

THERAPEUTIC INDICATIONS:

  • acute and chronic conjunctivitis;

  • blepharoconjunctivitis;

  • keratitis;

  • keratouveitis;

  • in preoperative and postoperative periods to prevent purulent-inflammatory complications;

  • in the treatment of eye injuries.

dwldDownload instructions for use

Composition

1 ml of the product contains:

  • active substance - benzyldimethyl [3-(myristoylamino)propyl] ammonium chloride monohydrate (in terms of anhydrous substance) - 0.1 mg;
  • excipients: sodium chloride 9.0 mg, water for injection up to 1 ml.

Pharmaceutical form

Eye drops 0.01%, 5 ml and 10 ml

Sense organs. Ophthalmologicals. Antimicrobials. Other antimicrobials.

ATC CODE S01AX.

Indications

  • acute and chronic conjunctivitis;
  • blepharoconjunctivitis;
  • keratitis;
  • keratouveitis;
  • in preoperative and postoperative periods to prevent purulent-inflammatory complications;
  • in the treatment of eye injuries.

Contraindications

  • individual intolerance to the product;
  • children under 18 years of age.

Posology and method of administration

The product is ready for use.

Topically. For therapeutic purposes, instill Mistinin-DF eye drops into the conjunctival sac in 1-2 drops 4-6 times a day until clinical recovery.

For preventive purposes, instill the product 2-3 days before surgery and for 10-15 days after surgery - 1-2 drops 3 times a day.

Adverse reactions

  • a slight burning sensation, discomfort that disappears on its own, after 15-20 seconds and does not require withdrawal of the product.

Rare:

  • allergic reactions.

Overdose

Cases of overdose are not marked.

Use during pregnancy and lactation

If it is necessary to prescribe the product during pregnancy and lactation, the expected benefit to the mother and the potential risk to the fetus should be assessed.

Pediatric population

Do not use in children under 18 years of age.

Special Warnings

Contact lenses should be removed immediately before the product is instilled and put on no earlier than 15 minutes after instillation.

Effects on ability to drive and use machines

During treatment it is necessary to refrain from driving motor transport and from other potentially dangerous activities that require high concentration, quick psychomotor reactions and good vision for 30 minutes after instillation into the eye.

Presentation and package

5 ml and 10 ml of the product in plastic dropper bottles, sealed with tamper-proof caps. Each bottle has a label made of label or writing paper.

One bottle with instructions for use in the state and Russian languages are placed in a carton pack made of chrome-ersatz.

Storage conditions

Store below 25 °С.

Keep out of the reach of children.

Shelf life

3 years.

Shelf life after opening the bottle - 1 month.

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: This email address is being protected from spambots. You need JavaScript enabled to view it.

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