Bonafton® (Ointment) Instructions for Use
ATC Code
D06BB (Antiviral drugs)
Clinical-Pharmacological Group
Antiviral drug for external and topical use
Pharmacotherapeutic Group
Antiviral agent for topical application
Pharmacological Action
Antiviral drug, active against Herpes simplex virus and some adenoviruses.
It suppresses the synthesis of cytoplasmic proteins that are incorporated into the capsids and disrupts the transport of viral capsid components into the cell nucleus where their assembly takes place.
Pharmacokinetics
Pharmacokinetic data for the drug are not available.
Indications
Viral diseases
- Of the skin;
- Of the mucous membranes of the oral cavity and genitals (herpes simplex, herpes zoster; condyloma acuminatum);
- Herpetic stomatitis and gingivitis.
ICD codes
| ICD-10 code | Indication |
| A60 | Anogenital herpesviral infection [herpes simplex] |
| A63.0 | Anogenital [venereal] warts (condyloma acuminatum) |
| B00 | Herpesviral [herpes simplex] infections |
| B00.2 | Herpetic gingivostomatitis and pharyngotonsillitis |
| B02 | Zoster [herpes zoster] |
| ICD-11 code | Indication |
| 1A94.Z | Anogenital herpes simplex virus infection without further specification |
| 1A95.Z | Anogenital warts, unspecified |
| 1E91.Z | Herpes zoster, unspecified |
| 1F00.0 | Infection of skin or mucous membranes caused by herpes simplex virus |
| 1F00.02 | Gingivostomatitis caused by herpes simplex virus |
| 1F00.Z | Infections due to herpes simplex virus, unspecified |
Dosage Regimen
| The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen. |
Ointment
Topically, externally.
For herpes simplex and herpes zoster, the drug is applied in a thin layer to the affected areas of the skin 3-4 times a day (in the genital area – 4-6 applications per day).
Treatment is carried out in 3 cycles of 5 days each with 1-2-day breaks or 2 cycles of 10 days each with a 3-5-day break.
For diseases of the oral mucosa, the drug is applied in a thin layer to the affected areas 4-6 times a day (the course of treatment is 3-20 days depending on the severity of the disease).
For the treatment of condyloma acuminatum, the drug is used 2 times a day for 2 weeks.
Treatment with the ointment is combined with oral administration of Bonafton® tablets, soluble in the intestine.
Adverse Reactions
Allergic reactions. Dermatitis.
Contraindications
- Hypersensitivity to the drug components;
- Pregnancy and lactation;
- Children under 18 years of age.
Use in Pregnancy and Lactation
Contraindicated during pregnancy and lactation.
Pediatric Use
Contraindicated in children under 18 years of age.
Special Precautions
Effect on the ability to drive vehicles and mechanisms
The drug does not have a negative effect on the performance of potentially hazardous activities requiring special attention and quick reactions (driving a car, etc.).
Overdose
To date, no cases of drug overdose have been reported.
Drug Interactions
No pharmacological interaction with other drugs has been identified.
Storage Conditions
At a temperature not exceeding 25°C (77°F). Keep out of reach of children.
Shelf Life
Shelf life – 2 years.
Dispensing Status
By prescription.
Important Safety Information
This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.
Medical DisclaimerBrand (or Active Substance), Marketing Authorisation Holder, Dosage Form
Ointment for topical and external use 0.5%: 15 g or 25 g tubes
Marketing Authorization Holder
Murom Instrument-Making Plant, FSUE (Russia)
Dosage Form
| Bonafton® | Ointment for topical and external use 0.5%: 15 g or 25 g tubes |
Dosage Form, Packaging, and Composition
Ointment for topical and external use from orange to brownish-orange in color.
| 100 g | |
| Bromonaphthoquinone | 0.5 g |
Excipients: petrolatum – up to 100 g.
15 g – aluminum tubes (1) – cardboard boxes.
25 g – aluminum tubes (1) – cardboard boxes.
Ophthalmic ointment 0.05%: 10 g tubes
Marketing Authorization Holder
Murom Instrument-Making Plant, FSUE (Russia)
Dosage Form
| Bonafton® | Ophthalmic ointment 0.05%: 10 g tubes |
Dosage Form, Packaging, and Composition
Ophthalmic ointment 0.05%.
| 100 g | |
| Bromonaphthoquinone | 50 mg |
10 g – aluminum tubes (1) – cardboard boxes.
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