Brilliant green

INSTRUCTIONS FOR MEDICAL USE OF THE MEDICINAL PRODUCT BRILLIANT GREEN

Composition:

Active substance: brilliant green;

100 ml of solution contain 1 g of brilliant green;

Excipient: ethanol 60 %.

Pharmaceutical form. 1% alcoholic solution for external use.

Main physicochemical properties: intensely green liquid with a characteristic odor of alcohol.

Pharmacotherapeutic group. Antiseptics and disinfectants. ATC code D08A X.

Pharmacological properties.

Pharmacodynamics.

An antiseptic agent for topical and local use. Exerts antimicrobial action. The drug is active against gram-positive bacteria.

Pharmacokinetics.

The drug is intended for local action. There is no data on absorption into the blood or participation in the body's metabolic processes.

Clinical characteristics.

Indications.

Skin purulent-inflammatory processes (pyoderma, furunculosis, carbunculosis, blepharitis) of mild form, as well as treatment of the surgical field, skin surfaces after surgeries and injuries.

Contraindications.

Hypersensitivity to the components of the drug.

Special precautions.

Avoid contact of the drug with eyes.

Do not violate the application instructions of the medicinal product, as this may harm health.

Interaction with other medicinal products and other types of interactions.

When used simultaneously with topical agents containing organic compounds, it may denature proteins and form new compounds.

Incompatible with disinfectants containing active iodine, chlorine, alkalis (including ammonia solution).

When using any other medicinal products concurrently, inform the physician.

Special precautions for use.

Avoid contact of the solution with mucous membranes, as the alcohol contained in the medicinal product may cause burns and severe irritation. The activity of the medicinal product is considerably reduced in the presence of blood serum.

Use during pregnancy or breastfeeding.

Can be used.

Ability to affect reaction rate when driving or operating machinery.

Does not affect.

Method of administration and dosage.

Apply to the skin surface, and in case of impaired integrity, include the surrounding healthy tissues. In eye diseases, apply to the edges of the eyelids.

Children.

Apply.

Overdose.

Not observed.

Adverse Reactions.

Allergic reactions (itching, urticaria). If the solution comes into contact with the eye mucosa, burning, lacrimation, and possible burns may occur.

In case of any adverse events, consult a physician immediately!

Shelf life. 2 years.

Do not use the medicinal product after the expiry date stated on the packaging.

Storage conditions.

Store in the original packaging at a temperature not exceeding 25 °C.

Keep out of reach of children.

Packaging. 10 ml or 20 ml in bottles; 20 ml in dropper bottles.

Availability classification. Over-the-counter.

Manufacturer. JSC "FITOFARM"

(responsible for batch release, excluding batch control/testing).

Manufacturer's address and location of business activity.

17, Chumatska St., Boryspil, Kyiv region, Ukraine, 08303.

Marketing Authorization Holder.

JSC "FITOFARM".

Reporting of adverse reactions after registration of the medicinal product is of great importance. It enables continuous monitoring of the benefit-risk balance of the medicinal product. Medical and pharmaceutical professionals, as well as patients or their legal representatives, are encouraged to report all suspected adverse reactions and lack of efficacy via the Automated Pharmacovigilance Information System at: https://aisf.dec.gov.ua.

In case of adverse reactions or any questions regarding safety, quality, or efficacy of the medicinal product, please contact the Pharmacovigilance Department of JSC "FITOFARM" at +38 (044) 390 52 96.

Address of the Marketing Authorization Holder.

7, Verkhovnoi Rady Blvd., premises 18, 3rd floor, Kyiv, Ukraine, 02100.

INSTRUCTIONS

for medical use of the medicinal product

BRILLIANT GREEN

Composition:

Active ingredient: brilliant green;

100 ml of solution contain 1 g of brilliant green;

Excipient: ethanol 60 %.

Pharmaceutical form. 1 % alcoholic solution for external use.

Main physicochemical properties: intense green liquid with the smell of alcohol.

Pharmacotherapeutic group. Antiseptics and disinfectants. ATC code D08A X.

Pharmacological Properties

Pharmacodynamics

An antiseptic agent for external and local use. Exerts antimicrobial action. The drug is active against gram-positive bacteria.

Pharmacokinetics

The drug is intended for local action. There are no data on absorption into the blood or participation in the body's metabolic processes.

Clinical characteristics.

Indications.

Skin purulent-inflammatory processes (pyoderma, furunculosis, carbunculosis, blepharitis) of mild form, as well as treatment of the surgical field, skin surfaces after surgery and trauma.

Contraindications.

Hypersensitivity to the components of the drug.

Special safety precautions.

Avoid getting the drug into the eyes.

Do not violate the rules of using the medicinal product, as this may harm health.

Interaction with other medicinal products and other types of interactions.

When used simultaneously with topical agents containing organic compounds, it may denature proteins and form new compounds.

Incompatible with disinfectant agents containing active iodine, chlorine, alkalis (including ammonia solution).

When using any other medicinal products concurrently, inform your doctor.

Special precautions.

Avoid contact of the solution with mucous membranes, as the alcohol contained in the preparation may cause burns and severe irritation. The activity of the preparation is considerably reduced in the presence of blood serum.

Use during pregnancy or breastfeeding.

Can be used.

Ability to affect reaction speed when driving or operating machinery.

Has no effect.

Method of administration and dosage.

Apply to the skin surface, and in case of impaired integrity, include the surrounding healthy tissues. In eye diseases, apply to the edges of the eyelids.

Children.

Apply.

Overdose.

Not observed.

Side effects.

Allergic reactions (itching, urticaria). If the solution gets onto the mucous membrane of the eye, burning, lacrimation, and possible burns may occur.

If any adverse events occur, consult a physician immediately!

Shelf life. 2 years.

Do not use the medicinal product after the expiry date stated on the packaging.

Storage conditions.

Store in the original packaging at a temperature not exceeding 25 °C.

Keep out of reach of children.

Packaging. 10 ml or 20 ml in bottles; 20 ml in dropper bottles.

Availability. Over-the-counter (without prescription).

Manufacturer.

JSC "PHYTOPHARM".

Manufacturer's address and location of business activity.

2 Sybirtseva Street, Bakhmut, Donetsk region, 84500, Ukraine.

Marketing Authorization Holder.

JSC "PHYTOPHARM".

Reporting of adverse reactions following registration of the medicinal product is highly important. It enables continuous monitoring of the benefit/risk ratio of the medicinal product. Healthcare and pharmaceutical professionals, as well as patients or their legal representatives, are encouraged to report all suspected adverse reactions and lack of efficacy via the Automated Information System for Pharmacovigilance at: https://aisf.dec.gov.ua.

In case of adverse reactions or questions regarding the safety, quality, and efficacy of the medicinal product, please contact the Pharmacovigilance Department of JSC "PHYTOPHARM" at +38 (044) 390 52 96.

Marketing Authorization Holder's address.

7, Verkhovnoi Rady Avenue, premises 18, 3rd floor, Kyiv, 02100, Ukraine.