BRILLIANT GREEN
UkraineThe drug is used to treat mild forms of purulent inflammatory skin processes (e.g., boils, carbuncles, pyoderma, blepharitis), as well as for skin treatment after injuries or surgeries.
Frequently asked questions
How should the product be used correctly?
Apply the solution to the skin. If the skin is damaged, treat the surrounding healthy tissue as well. For eye diseases, lubricate the edges of the eyelids.
Can Brilliant green be used during pregnancy or breastfeeding?
Yes, the drug can be used during these periods.
What are the possible side effects of Brilliant green?
Allergic reactions, such as itching or urticaria, are possible. If it comes into contact with the mucous membrane of the eye, burning, tearing, or burns may occur.
Who should not use this drug?
The product should not be used in case of hypersensitivity to its components.
What should be avoided during use?
Do not allow the solution to get into the eyes or onto mucous membranes, as the alcohol in the composition may cause irritation or burns.
How does the drug interact with other substances?
It must not be combined with disinfectants containing iodine, chlorine, or alkalis (including ammonia solution). When used with other skin medications, the properties of the substances may change. Any simultaneous use of other medicines should be reported to a physician.
Instructions for use
I N S T R U C T I O N 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. Topical solution, alcoholic.
Main physicochemical properties: intense green-colored liquid with a characteristic odor of alcohol.
Pharmacotherapeutic group.
Antiseptics and disinfectants. ATC code D08AX.
Pharmacological properties.
Pharmacodynamics.
An antiseptic agent for external and local use. Exerts antimicrobial action. The drug is active against gram-positive bacteria.
Pharmacokinetics.
Local action agent. There are no data on absorption into the blood or participation in the body's metabolic processes.
Clinical characteristics.
Indications.
Purulent-inflammatory skin conditions (pyoderma, furunculosis, carbunculosis, blepharitis) of mild form, as well as treatment of surgical sites and skin surfaces following surgery or trauma.
Contraindications.
Hypersensitivity to the components of the drug.
Special safety precautions.
Avoid contact of the drug with eyes.
Do not violate the application instructions, 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 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.
Does not affect.
Method of administration and dosage.
Apply to the skin surface, covering the surrounding healthy tissues when their integrity is compromised. In eye diseases, apply to the edges of the eyelids.
Children.
Use as directed.
Overdose.
Not observed.
Side effects.
Allergic reactions (itching, urticaria). If the solution gets on the eye's mucous membrane, burning, tearing, and possible burns may occur.
If any adverse events occur, consult a physician.
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. 15 ml or 20 ml in bottles. 1 bottle per pack or without a pack.
Supply category. Over-the-counter.
Manufacturer. JSC Pharmaceutical Factory "Viola".
Manufacturer's address and place of business.
69063, Zaporizhzhia, Amosova St., 75, Ukraine.
Marketing Authorization Holder. JSC Pharmaceutical Factory "Viola".
Address of the Marketing Authorization Holder.
69063, Zaporizhzhia, Amosova St., 75, Ukraine.
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