PACKAGE LEAFLET: INFORMATION FOR THE USER
ARKOCAPSULES NETTLE ROOT 290 mg hard capsules
Urtica dioicaL. andUrtica urensL.
Contents of the package leaflet:
Traditional herbal medicinal product for the relief of symptoms such as difficulty in urination and discomfort of the urinary tract in patients who have been informed that they suffer from benign prostatic hyperplasia. The use of this medicinal product in this specific indication is based exclusively on its traditional use.
Before starting treatment, the doctor should have ruled out any serious condition of the disease.
You should consult a doctor if it worsens or does not improve after 14 days.
Do not take ARKOCAPSULES NETTLE ROOT
If you are allergic to the active ingredient or to any of the other components of ARKOCAPSULES NETTLE ROOT.
Warnings and precautions
Consult your pharmacist, doctor, or nurse before starting to take ARKOCAPSULES NETTLE ROOT.
Children and adolescents
Children and adolescents under 18 years of age should not use this medicinal product. This medicinal product is not intended for this population.
Use of ARKOCAPSULES NETTLE ROOT with other medicinal products
Inform your pharmacist or doctor if you are using, have recently used, or may need to use any other medicinal product.
Taking ARKOCAPSULES NETTLE ROOT with food and drinks
Food and drinks do not have an influence on the effect of the medicinal product.
Pregnancy, breastfeeding, and fertility
The use of ARKOCAPSULES NETTLE ROOT is not indicated in women.
Driving and using machines
No effects on the ability to drive and use machines have been described.
Follow exactly the administration instructions of the medicinal product contained in this package leaflet or as indicated by your pharmacist, doctor, or nurse. In case of doubt, ask your pharmacist, doctor, or nurse.
The recommended dose is:
Adults: take 2 or 3 capsules, twice a day, with a glass of water.
This medicinal product is for oral use.
Use for a treatment period of 2 weeks.
Use in children and adolescents
Do not use in children and adolescents under 18 years of age. This medicinal product is not intended for this population.
If you take more ARKOCAPSULES NETTLE ROOT than you should
No cases of overdose with ARKOCAPSULES NETTLE ROOT have been described.
In case of overdose or accidental ingestion, consult your pharmacist or doctor immediately or call the Toxicology Information Service, telephone 91 562 04 20, indicating the medicinal product and the amount ingested.
If you forget to take ARKOCAPSULES NETTLE ROOT
In case of forgetting a dose, take the medicinal product as soon as possible, continuing the treatment as prescribed. However, if the next dose is near, it is better not to take the forgotten dose and wait for the next one. In no case take a double dose to compensate for the forgotten dose.
Like all medicinal products, ARKOCAPSULES NETTLE ROOT can cause side effects, although not everybody gets them.
At the recommended doses, ARKOCAPSULES NETTLE ROOT does not present side effects.
If you experience side effects, consult your pharmacist, doctor, or nurse, even if it is a side effect not listed in this package leaflet.
Keep out of the reach and sight of children.
Do not store above 25°C.
Expiry date:
Do not use ARKOCAPSULES NETTLE ROOT after the expiry date stated on the package, after the abbreviation “EXP”. The expiry date is the last day of the month indicated.
Medicinal products should not be disposed of via wastewater or household waste. Deposit the packages and medicinal products that you no longer need in the SIGRE collection point at the pharmacy. In case of doubt, ask your pharmacist how to dispose of the packages and medicinal products that you no longer need. This way, you will help protect the environment.
Composition of ARKOCAPSULES NETTLE ROOT
Each capsule contains as active ingredient: 290 mg of cryomilled roots of Urtica dioicaL. and Urtica urensL. (Nettle root).
The other components are the excipients: hypromellose (capsule shell).
Appearance of the product and package contents
There is one presentation in bottles containing 48 capsules.
Marketing authorization holder and manufacturer:
Holder
ARKOPHARMA LABORATORIOS, S.A.U.
C/ Amaltea, 9
28045 MADRID
Manufacturer
ARKOPHARMA
LABORATOIRES PHARMACEUTIQUES
BP 28 – 06511 CARROS Cedex - FRANCE
This package leaflet was approved in January 2019
“Detailed and updated information on this medicinal product is available on the website of the Spanish Agency for Medicinal Products and Medical Devices (AEMPS)