About the medicine
- Active ingredients
- Диметинден + Фенилэфрина гидрохлорид
- Strength
- 2.5 мг + 0.25 мг
- Dosage form
- Капли назальные
- Manufacturer
- Рубикон (Беларусь)
- Dispensing
- Over the counter
- Registration certificate
- РК-ЛС-5№025715
- Registered
- 11 Apr 2022
- Registration valid until
- 2 May 2028
- Shelf life
- 3 год
- Country of registration
- Kazakhstan
Packs 1
- По 15 мл во флаконе. Флакон в пачке из картона.
Package leaflet
There is no leaflet with these active ingredients in the reference yet. Read the leaflet in the pack and ask a doctor or pharmacist.
Other forms and manufacturers
This is reference information and does not replace a doctor's advice. Do not self-medicate: read the leaflet and ask a specialist before use.
Source: State Register of Medicines of the Republic of Kazakhstan (register.ndda.kz).