Zoderm
Natural health product licensed in Canada
- Other names
- Capsidol, Proderm
- Licence holder
- Euro-Pharm International Canada Inc.
- NPN or DIN-HM
- 80006583
- Status
- Active licence
- Licence date
- 14 July 2008
- Revision date
- Not provided
- Form
- Crème
- Route of administration
- Topique
- Application type
- Officinale
Oral dose analysis does not apply without an established exclusively oral route.
Composition
Medicinal composition not provided.
Non-medicinal ingredients
Edetate Disodium, Eau purifiée, propylèneglycol, butylated hyroxyanisole, Myristate d'isopropyle, White Wax, Glycérine, (p)-hydroxybenzoate de méthyle, Alcool cétostéarylique, Acide stéarique, (p)-hydroxybenzoate de propyle
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Adultes | Not specified | Not specified | 4 Tous les jours |
Uses authorised in Canada
Traditionally used in Herbal Medicine as a rubefaclent/countorinitant to help relieve the symptoms of rheumatism and /or muscle and joint pain. Used for the temporary relief of muscle and joint pain associated with rheumatoid arthritis, and pain of tendons and ligaments.
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
Consult a health care practitioner if symptoms persist or worsen. Avoid applying to injured or broken skin.
Source
Official Health Canada record, licence 80006583
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.