Instructions for use SeptoZinc eye drops, bottle 10 ml
COMPOSITION
Sodium chloride, 7.5 mg per 1 ml (0.75%)
Excipients: benzalkonium chloride - 0.2 mg in 1 ml (0.02%); zinc gluconate - 1 mg/ml (0.1%); potassium chloride; magnesium chloride hexahydrate; calcium chloride dihydrate; sodium citrate; purified water.
FORM OF RELEASE
Eye drops with zinc, sterile, 10 ml.
FEATURES
SeptoZinc eye drops are a sterile, isotonic solution for rinsing, with the addition of synergistic substances (zinc gluconate and benzalkonium chloride). It is intended for instillation into the eyes and rinsing the eyes.
The beneficial antimicrobial properties of compounds containing zinc ions in ophthalmic preparations have been known for a long time. The antimicrobial activity of zinc ions is associated with their ability to coagulate the proteins of microorganisms with the formation of albuminates. Due to the coagulation of the surface layers, bacteria are deprived of their nutrient medium, which facilitates their excretion. Some types of bacilli release exogenous proteolytic enzymes that cause maceration of the corneal epithelium. Zinc inhibits the release of these proteolytic enzymes. Also, zinc in the form of gluconate reacts with proteins on the surface of the conjunctiva and forms a protective layer under which cell regeneration occurs, which contributes to the restoration of the physiological state of the conjunctiva. Zinc ions reduce the permeability of the cell membrane and capillary membrane and thus reduce swelling, secretion and mucus formation in case of catarrhal inflammation of the mucous membrane of the eye. When applied topically, zinc has an astringent and anti-inflammatory effect.
In bezalkonium chloride eye drops, it is used as a preservative, and in higher concentrations, it acquires antiseptic properties.
INDICATION
SeptoZinc eye drops are intended for use in adults, adolescents and children over 1 year of age.
SeptoZINC can be used as a concomitant or complex therapy in the presence of inflammatory diseases of the anterior segment of the eye of microbial etiology (keratitis, blepharitis), inflammatory reactions of the conjunctiva after surgical interventions and for the prevention of infectious inflammation of the eyes (including foreign body ingress into the eye or for the sanitation of the eye microflora).
CONTRAINDICATION
Hypersensitivity or allergy to the active substance or any of the excipients that make up SeptoZINC.
INTERACTION WITH MEDICINES
So far, no relevant notifications have been received.
If you use any other eye drops or eye ointments, they should be administered no earlier than 5 minutes after using SeptoZINC.
APPLICATION FEATURES
Use during pregnancy or breastfeeding.
Since there is no experience with the use of SeptoZINC in pregnant and lactating women, the risk/benefit ratio should be considered. During pregnancy and lactation, consultation and permission from a doctor is required for their use.
Contact lenses. Patients should not wear soft contact lenses (especially hydrophilic lenses) during the period of application of SeptoZinc. If possible, hard contact lenses should not be worn during the period of treatment, or the patient should remove them before instillation and re-insert them no earlier than 20 minutes after application of SeptoZinc.
Ability to influence the reaction rate when driving vehicles or other mechanisms. Eye drops SeptoZinc do not affect the reaction rate when driving vehicles, equipment and working at heights, which require increased attention. However, after instillation into the conjunctival sac, temporary blurred vision is possible, therefore, activities requiring increased attention can be started only after this temporary effect has passed.
If a child accidentally swallows SeptoZinc, consult a doctor.
METHOD OF ADMINISTRATION AND DOSAGE
SeptoZinc eye drops can be used for instillation into the eyes and/or for simple short-term eye rinsing without consulting an ophthalmologist.
Dosage.
To relieve symptoms in the eyes and support during treatment for infections of the conjunctiva of the eyes and eyelids, SeptoZinc should be instilled into the lower conjunctival sac 1 drop 3 times a day.
The duration of use (on average) can be from one to three weeks, it is selected individually, depending on the severity and course of the disease: usually until the symptoms disappear completely.
Reservation.
Caution is required in the presence of dry eye syndrome and other ocular surface diseases. In the presence of this syndrome, the recommended duration of use should not exceed 14 days.
If the intensity of the symptoms for which you used SeptoZinc has not decreased and they persist for more than two days, or worsen, you should seek advice from an ophthalmologist.
After opening the bottle, Septozink is ready for instillation into the eyes. The patient should remove the protective cap, tilt their head back slightly, turn the bottle upside down and squeeze the plastic bottle to instill the required number of drops into the lower conjunctival sac. The amount of solution used depends on the method of use. Septozink should be instilled or the affected eye should be rinsed with it as needed (the amount of solution flowing out of the bottle is controlled by squeezing the bottle). During instillation, the tip of the bottle should not touch the surface of the eye, eyelids or eyelashes. After use, the cap should be securely screwed on to avoid accidental contamination of the solution. The bottle should be stored in an upright position.
SIDE EFFECT
SeptoZinc eye drops are very well tolerated. Rarely, a temporary slight burning sensation may occur immediately after application. Hypersensitivity reactions are also possible. If these side effects or any other unusual reactions occur, you should inform your doctor or pharmacist.
EXPIRATION DATE
2 years. After first opening the original bottle - store for no more than 28 days. Do not use after the expiry date which is stated on the label or carton next to the hourglass icon. The expiry date refers to the last day of that month.
STORAGE CONDITIONS
Do not refrigerate/freeze.
Store in the original packaging, out of the reach of children, at a temperature not exceeding 25 °C.
NOT A MEDICINE. AVAILABLE WITHOUT A PRESCRIPTION.
PRODUCER
"UNIMED PHARMA, spool s.r.o.", Orieškova, 11, 821 05, Bratislava, Slovak Republic
Unimed Pharma, spol. s ro, Oriešková 11, 821 05, Bratislava, Slovak Republic
Authorized representative of the manufacturer in Ukraine:
Representative office of "UNIMED PHARMA, spool s r.o.", P. Myrnogo St., 16/13 (letter A), Kyiv, 01001, Ukraine
Tel. +380689614144, e-mail: unimedpharma@unimedpharma.com.ua
