Venaforce 20 mg
Natural health product licensed in Canada
- Licence holder
- Bioforce Canada Inc.
- NPN or DIN-HM
- 80001109
- Status
- Inactive licence
- Licence date
- 7 December 2005
- Revision date
- Not provided
- Form
- Comprimé
- 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 composition not provided.
Non-medicinal ingredients
Polysaccharides de soja, Talc, Dioxyde de silicium colloïdal, Starch, Corn, Methacrylic copolymer, Triethyl citrate, Cellulose - microcrystalline
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Adultes | Not specified | 2 Comprimé | 3 Tous les jours |
Uses authorised in Canada
Traditionally used for the symptomatic treatment associated with venous insufficiency and varicose veins.
A use authorised in Canada is not an authorised health claim in the European Union. See the health claims register.
Warnings in Canada
- Précautions et mises en garde
Avoid taking in case of known allergy to any of the known ingredients of the product. Consult a health care practitioner if you have bleeding disorders. Consult a health care practitioner if symptoms persist.
- Contre-indications
Do not use if you are pregnant or breastfeeding. Do not use if you have impaired heart, kidney and/or liver functions.
Source
Official Health Canada record, licence 80001109
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.