MED-FLEX
Natural health product licensed in Canada
- Other names
- FLO-FLEX, X-DOL
- Licence holder
- Medelys Laboratoires International Inc.
- NPN or DIN-HM
- 80019384
- Status
- Active licence
- Licence date
- 8 June 2010
- Revision date
- Not provided
- Form
- Liquide
- Route of administration
- Topique
- Application type
- TPD Cat IV/LS
Oral dose analysis does not apply without an established exclusively oral route.
Composition
| Medicinal ingredient and source | Per dosage unit, according to the source |
|---|---|
| Eugenia caryophyllata | 0.8 % |
Non-medicinal ingredients
Camphre, Menthe poivrée, Lavande
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Adultes | Not specified | 1 Pulvérisateur | minimum: 3 Tous les jours ; maximum: 4 Tous les jours |
| Enfants | minimum: 12 years | 1 Pulvérisateur | minimum: 3 Tous les jours ; maximum: 4 Tous les jours |
Uses authorised in Canada
Vaporisateur externe pour le soulagement temporaire des douleurs musculaires et des articulations dues aux contusions.
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.
Warnings are available in English on the official record.
Source
Official Health Canada record, licence 80019384
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.