BRILLIANT GREEN

Ukraine

The drug is used to treat mild forms of purulent skin inflammation (e.g., boils, carbuncles, pyoderma, blepharitis), as well as for skin treatment after injuries or surgeries.

Brand name BRILLIANT GREEN
Dosage form solution, alcoholic, for external use
Active substance / Dosage
brilliant green · 1 g/100 g
Prescription type over-the-counter (OTC)
ATC code
Registration number UA/8011/01/01
BRILLIANT GREEN solution, alcoholic, for external use

Frequently asked questions

How should the drug be applied correctly?

The solution should be applied to the skin. If there is skin damage, the surrounding healthy tissue should also be covered. For eye diseases, the edges of the eyelids must be lubricated.

Can BRILLIANT GREEN VIRIDENITENS be used by children and pregnant women?

The drug can be used by children, as well as by women during pregnancy or breastfeeding.

Who should not use this product?

The drug should not be used by people with increased sensitivity to its components.

What are the possible side effects of BRILLIANT GREEN VIRIDENITENS?

Allergic reactions, such as itching or urticaria, are possible. If it comes into contact with the eyes, burning, tearing, or burns may occur.

What should be avoided during use?

Do not allow the solution to come into contact with the eyes or mucous membranes, as the alcohol in the composition may cause irritation or burns. It is also not recommended to mix the product with disinfectants containing iodine, chlorine, or alkalis (including ammonia solution).

Does the drug affect the ability to drive a vehicle?

No, the drug does not affect reaction speed.

Instructions for use

INSTRUCTION FOR MEDICAL USE OF THE MEDICINAL PRODUCT BRILLIANT GREEN VIRIDENITENS

Composition:

Active substance: brilliant green;

100 g of solution contain brilliant green – 1 g;

Excipient: ethanol 60 %.

Pharmaceutical form. 1 % alcoholic solution for external use.

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

Pharmacotherapeutic group.
Antiseptics and disinfectants. ATC code D08AX.

Pharmacological properties.

Pharmacodynamics.

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

Pharmacokinetics.

Agent for local action. There is no data on absorption into the blood and participation in the body's metabolic processes.

Clinical characteristics.

Indications.

Skin infections and inflammatory conditions (pyoderma, furunculosis, carbunculosis, blepharitis) of mild form, as well as treatment of surgical sites and skin surfaces after surgery or trauma.

Contraindications.

Hypersensitivity to the components of the drug.

Special precautions.

Avoid contact of the drug with eyes.

Do not violate the instructions for use 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, or alkalis (including ammonia solution).

When using any other medicinal products concurrently, inform your 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 speed when driving or operating machinery.

No effect.

Method of administration and dosage.

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

Children.

To be used.

Overdose.

Not observed.

Side effects.

Allergic reactions (itching, urticaria). When the solution gets on the eye's mucous membrane, burning, lacrimation may occur, and burns may develop.

In case of any adverse events, consult a doctor!

Shelf life.

2 years.

Do not use the 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.

25 ml in a dropper bottle; 25 ml in a dropper bottle, 1 dropper bottle per carton.

Prescription status.

Over-the-counter.

Manufacturer.

PJSC "Halychpharm".

Manufacturer's address and place of business.

Ukraine, 79024, Lviv, Opryshkivska St., 6/8.

INSTRUCTION

for medical use of medicinal product

BRILLIANT GREEN

VIRIDE NITENS

Composition:

Active ingredient: brilliant green;

100 g of solution contains 1 g of brilliant green;

Excipient: ethanol 60%.

Pharmaceutical form: 1% alcoholic solution for topical use.

Main physicochemical properties: transparent, intensely green liquid with a characteristic alcoholic odor.

Pharmacotherapeutic group.

Antiseptics and disinfectants. ATC code D08AX.

Pharmacological properties.

Pharmacodynamics.

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

Pharmacokinetics.

The drug acts locally. No data on absorption into the bloodstream or participation in the body's metabolic processes have been identified.

Clinical characteristics.

Indications.

Mild forms of purulent-inflammatory skin conditions (pyoderma, furunculosis, carbunculosis, blepharitis), as well as treatment of surgical fields, skin after surgery and trauma.

Contraindications.

Hypersensitivity to the components of the drug.

Special precautions.

Avoid contact of the drug with eyes.

Do not violate the instructions for use 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, or alkali (including ammonia solution).

Inform your doctor if using any other medicinal products concurrently.

Special instructions for use.

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

Use during pregnancy or breastfeeding.

Permitted.

Ability to affect reaction speed when driving or operating machinery.

Does not affect.

Dosage and administration.

Apply to the skin surface, and when skin integrity is compromised, include surrounding healthy tissue. In eye diseases, apply to the edges of the eyelids.

Children.

Permitted.

Overdose.

Not observed.

Side effects.

Allergic reactions (itching, urticaria). When the solution comes into contact with the eye's mucous membrane, burning, lacrimation, and burns may occur.

In case of any adverse events, consult a doctor!

Shelf life.

2 years.

Do not use the 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.

25 ml in a dropper bottle; 25 ml in a dropper bottle, 1 dropper bottle per carton.

Prescription status.

Over-the-counter.

Manufacturer. PJSC "Halychpharm".

Manufacturer's address and place of business.

Ukraine, 79024, Lviv, Opryshkivska St., 6/8.

Similar drugs

The original data is available in the language of the country of manufacture.

Data source: State Register of Medicinal Products of Ukraine

Data last verified: August 13, 2026