Euro K 8
Natural health product licensed in Canada
- Licence holder
- Euro-Pharm International Canada Inc.
- NPN or DIN-HM
- 02242291
- Status
- Inactive licence
- Licence date
- 4 December 2007
- Revision date
- Not provided
- Form
- Comprimé
- Route of administration
- Orale
- Application type
- DIN de transition
If this product were sold in France
No point flagged by the rules we apply.
A daily quantity is calculated only for an explicit adult oral dosage, stated per day and in a solid unit matching the product form. Ambiguous units, liquids, powders and paediatric doses are not extrapolated. A quantity not calculated is not compared with dose limits. This analysis does not constitute authorisation for sale in France or an assessment of safety or efficacy.
Composition
| Medicinal ingredient and source | Per dosage unit, according to the source | Maximum per day, adult |
|---|---|---|
| Potassium Source : Chlorure de potassium Potency : 8 mmol | 600 mg | Not calculated |
Non-medicinal ingredients
Eau, Silicon dioxide colloïdal, Stéarate de magnésium, FD & C Jaune no. 6, Dioxyde de titane, Hydroxy methyl cellulose, Gélatine, Acide stéarique, Méthylcellulose
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Adultes | Not specified | minimum: 5 Capsule ; maximum: 12 Capsule | minimum: 2 Tous les jours ; maximum: 4 Tous les jours |
| Adultes | Not specified | minimum: 3 Capsule ; maximum: 5 Capsule | minimum: 2 Tous les jours ; maximum: 4 Tous les jours |
Uses authorised in Canada
Treatment or prevention of hypokalemia which does not result from dietart deficiency. Treatment of digitalis toxicity. Potassium replacement therapy. Electrolyte replenisher. For the treatment of metabolic alkalosis.
A use authorised in Canada is not an authorised health claim in the European Union. See the health claims register.
Warnings in Canada
No French warning text available in the imported data.
Source
Official Health Canada record, licence 02242291
Licensed Natural Health Products Database (LNHPD), Health Canada: licensed products, ingredients, doses, uses and risks, retrieved 27 October 2026.
Contains information licensed under the Open Government Licence – Canada (Health Canada, LNHPD)
Licence du gouvernement ouvert – Canada 2.0 (OGL-Canada 2.0)
The formula sold in Europe under the same name may differ. This information does not replace advice from a doctor or pharmacist.
The evidence date of this ingredient list is unknown.
Has the product changed? Photograph the packaging.