Duraflor®
Natural health product licensed in Canada
- Licence holder
- AMD Medicom Inc.
- NPN or DIN-HM
- 80014081
- Status
- Active licence
- Licence date
- 19 October 2009
- Revision date
- Not provided
- Form
- Liquide
- Route of administration
- Dentaire
- 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 |
|---|---|
| Fluorure de sodium Source : Fluorure de sodium | 5 % (p/p) |
Non-medicinal ingredients
Rosin, xylitol, Sucralose, alcool dénaturé, Bubblegum flavour, Cire d'abeille jaune, Saveur de framboise
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Adultes | Not specified | 5 Goutte(s) | Not specified |
| Enfants | Not specified | 2 Goutte(s) | Not specified |
Uses authorised in Canada
Text supplied in English because no French text is available.
Anti-caries. Anti-cavity Preparation
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 80014081
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.