€ 19,00
1 in stock
IDROFLOG
Composition
Sodium hyaluronate 2 mg/ml, sodium phosphate hydrocortisone 10 mcg/ml, trisodium citrate, sodium chloride, potassium chloride, magnesium chloride, dibasic sodium phosphate, monobasic sodium phosphate, water for injections.
Usage instructions
IDROFLOG must be dosed individually according to one’s condition and based on the recommendations of one’s ophthalmologist. In general, instill 1-2 drops of the solution into the conjunctival sac of the eye to be treated, 2-4 times a day. The total duration of treatment is 2-6 months but must be specifically established by the specialist doctor and always under their direct control (a follow-up every 30-45 days is recommended).
Detach a single vial from the strip. Remove the upper cap by twisting it.
Instill 1-2 drops into the conjunctival sac, letting them fall from above.
IDROFLOG can also be used while wearing contact lenses.
Warnings
When not to use:
– hypersensitivity to the components or other chemically related substances;
– in conjunction with viral contamination of the ocular surface, corneal ulcers, eye mycosis, purulent conjunctivitis, purulent and herpetic blepharitis, stye;
– generally contraindicated in pregnancy, during breastfeeding, and in pediatric age.
The product, due to its viscoelastic properties, may cause temporary blurred vision upon instillation. Wait for this effect to subside before driving vehicles or using machinery.
IDROFLOG is for external use only.
IDROFLOG should not be used immediately before administering medications for therapeutic purposes, and within twenty minutes after the application of any topical drug therapy. If during treatment there is a worsening of eye symptoms, contact the doctor as soon as possible. Prolonged use may lead to inconveniences: the total duration of treatment must be established by the ophthalmologist. In case an inflammatory process is already underway, the specialist doctor will decide on the appropriate anti-inflammatory therapy to restore physiological conditions of the ocular surface.
To reduce the risk of contamination during use, it is advisable to open the aluminum pouch only in case of immediate subsequent use of the product. Avoid direct contact of the vial tip with fingers, the eye, or any other surface.
In rare cases, a slight blurring of vision has been observed upon instillation, which is due to the viscosity of the solution. A slight burning sensation may occur during instillation. However, this sensation is expected to disappear. Contact your ophthalmologist if symptoms persist. Following the instructions in the package leaflet reduces the risk of undesirable effects.
Do not use IDROFLOG after the expiration date indicated on the packaging. The expiration date refers to the intact and properly stored product.
Keep out of sight and reach of children.
IDROFLOG must be used under the advice of a specialist doctor.
Storage
Store at a temperature between 2 °C and 25 °C.
Format
Pack containing 15 vials of 0.5 ml.
€ 19,00
1 in stock
IDROFLOG
Composition
Sodium hyaluronate 2 mg/ml, sodium phosphate hydrocortisone 10 mcg/ml, trisodium citrate, sodium chloride, potassium chloride, magnesium chloride, dibasic sodium phosphate, monobasic sodium phosphate, water for injections.
Usage instructions
IDROFLOG must be dosed individually according to one’s condition and based on the recommendations of one’s ophthalmologist. In general, instill 1-2 drops of the solution into the conjunctival sac of the eye to be treated, 2-4 times a day. The total duration of treatment is 2-6 months but must be specifically established by the specialist doctor and always under their direct control (a follow-up every 30-45 days is recommended).
Detach a single vial from the strip. Remove the upper cap by twisting it.
Instill 1-2 drops into the conjunctival sac, letting them fall from above.
IDROFLOG can also be used while wearing contact lenses.
Warnings
When not to use:
– hypersensitivity to the components or other chemically related substances;
– in conjunction with viral contamination of the ocular surface, corneal ulcers, eye mycosis, purulent conjunctivitis, purulent and herpetic blepharitis, stye;
– generally contraindicated in pregnancy, during breastfeeding, and in pediatric age.
The product, due to its viscoelastic properties, may cause temporary blurred vision upon instillation. Wait for this effect to subside before driving vehicles or using machinery.
IDROFLOG is for external use only.
IDROFLOG should not be used immediately before administering medications for therapeutic purposes, and within twenty minutes after the application of any topical drug therapy. If during treatment there is a worsening of eye symptoms, contact the doctor as soon as possible. Prolonged use may lead to inconveniences: the total duration of treatment must be established by the ophthalmologist. In case an inflammatory process is already underway, the specialist doctor will decide on the appropriate anti-inflammatory therapy to restore physiological conditions of the ocular surface.
To reduce the risk of contamination during use, it is advisable to open the aluminum pouch only in case of immediate subsequent use of the product. Avoid direct contact of the vial tip with fingers, the eye, or any other surface.
In rare cases, a slight blurring of vision has been observed upon instillation, which is due to the viscosity of the solution. A slight burning sensation may occur during instillation. However, this sensation is expected to disappear. Contact your ophthalmologist if symptoms persist. Following the instructions in the package leaflet reduces the risk of undesirable effects.
Do not use IDROFLOG after the expiration date indicated on the packaging. The expiration date refers to the intact and properly stored product.
Keep out of sight and reach of children.
IDROFLOG must be used under the advice of a specialist doctor.
Storage
Store at a temperature between 2 °C and 25 °C.
Format
Pack containing 15 vials of 0.5 ml.
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