Fukorcin
Ukraine
INSTRUCTION |
FUCORCIN |
Composition:active substances: basic fuchsin, boric acid, phenol, acetone, resorcinol; 1 ml of solution contains 0.004 g of basic fuchsin, 0.008 g of boric acid, 0.039 g of phenol, 0.049 ml of acetone, 0.078 g of resorcinol; excipients: ethanol 96%, purified water. |
| Pharmaceutical form. Alcoholic solution for external use. Main physicochemical properties: dark red liquid with a characteristic phenol odor. |
| Pharmacotherapeutic group. Antiseptics and disinfectants. ATC Code D08A X. |
Pharmacological properties.Pharmacodynamics. Active ingredients contained in the medicinal product provide a broad spectrum of antimicrobial effects in skin infections caused by infectious agents. The drug also exhibits fungicidal activity against fungal lesions of external coverings. |
Clinical characteristics.Indications. Treatment of skin diseases caused by pathogens sensitive to the components of the drug: various types of dermatophytes (trichophytons, microsporums, epidermophytons), microbial eczema, seborrhea of greasy and mixed forms. |
| Contraindications. Individual hypersensitivity to the components of the drug. Chronic allergic dermatoses. |
| Interaction with other medicinal products and other types of interactions. Concomitant use of topical antifungal antibiotics such as griseofulvin, clotrimazole, and products containing phenol or boric acid, as well as hormonal preparations, should be avoided. Allergic reactions may occur when used simultaneously with topical medicinal products. When using any other medicinal products concomitantly, inform your physician. |
Special precautions.The treatment with the medicinal product should be carried out under medical supervision and in accordance with the recommended doses. Avoid contact of the medicinal product with eyes and do not apply it on mucous membranes. Patients with impaired renal function must consult a physician before using the medicinal product. Do not violate the recommended application instructions, as this may harm your health. Use during pregnancy or breastfeeding. Do not use in women during pregnancy or breastfeeding. Effect on ability to drive or operate machinery. No effect on the ability to drive or operate machinery has been observed. |
Method of administration and dosage.Apply the solution to affected skin areas 1 to 3 times daily until symptoms disappear. The duration of treatment is determined by a physician. Children. Do not use in children under 12 years of age. |
| Overdose. With prolonged use of the medicinal product or application over large areas of skin, symptoms typical of phenol poisoning (dizziness, weakness, respiratory disturbances, collapse) may occur. In such cases, ensure access to fresh air, wash the medicinal product off the skin with water, and administer symptomatic treatment. In case of overdose, adverse effects and allergic reactions may intensify. Symptomatic therapy is recommended. |
Adverse reactions.Short-term sensation of burning and pain may occur. Hypersensitivity reactions including dermatitis, anaphylactic shock, urticaria, angioneurotic edema; local allergic reactions (e.g. rash, erythema, swelling, itching at the application site). In some patients, especially with prolonged use, systemic effects due to resorption may cause dizziness, weakness, respiratory disturbances, seizures, confusion, nausea, vomiting, headache, diarrhea, oliguria, and epithelial desquamation. If such symptoms occur, wash off any residual medicinal product from the skin surface with water, discontinue use of the product, and apply symptomatic therapy. In case of any adverse events, consult a physician. |
| 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, in a place inaccessible to children, at a temperature not exceeding |
| Packaging. 25 ml in bottles. |
| Prescription category. Over-the-counter. |
| Manufacturer. PP "Kilaff". |
| Address. Ukraine, 40035, Sumy region, Sumy, Kharkivska str., 6. |