Améa Arthri
Natural health product licensed in Canada
- Licence holder
- les Laboratoires Améa Ltée
- NPN or DIN-HM
- 80029167
- Status
- Active licence
- Licence date
- 24 January 2012
- Revision date
- Not provided
- Form
- Capsule
- Route of administration
- Orale
- Application type
- Officinale
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 |
|---|---|---|
| (Bis)méthanesulfonyle Source : Sulfone de diméthyl | 100 mg | Not calculated |
| Sulfate de 2-Amino-2-désoxy-D-glucose Source : Exosquelette de crevette (KCl) | 200 mg | Not calculated |
Non-medicinal ingredients
Hypromellose, Hydrolysat de collagène, Poudre de fleurs de tilleul, Stéarate de magnésium, Vinaigre de cidre
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Adultes | minimum: 19 years | 1 Capsule | 3 Tous les jours |
Uses authorised in Canada
Utilisée en phytothérapie pour aider à soulager la douleur articulaire associée à l'arthrose.
A use authorised in Canada is not an authorised health claim in the European Union. See the health claims register.
Warnings in Canada
- Effets indésirables connus
Certaines personnes pourraient souffrir de légers ballonnements gastro-intestinaux, de constipation ou d'indigestion. Une hypersensibilité ou une allergie au tilleul peuvent se manifester. Si tel est le cas, cesser l'utilisation.
Source
Official Health Canada record, licence 80029167
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.