Duraflor 5% Sodium Fluoride Varnish

Natural health product licensed in Canada

Licence holder

AMD Medicom Inc.

NPN or DIN-HM

80022817

Status

Active licence

Licence date

14 December 2010

Revision date

6 January 2026

Form

Liquide

Route of administration

Dentaire

Application type

Non traditionnelle

Composition

Medicinal composition not provided.

Non-medicinal ingredients

Hydroxyde de sodium, Sucralose, xylitol, Sodium salt of hydrogenated rosin, Bubblegum flavour (artificial), alcool dénaturé, Cire d'abeille jaune

Recommended doses in Canada

Uses authorised in Canada

Text supplied in English because no French text is available.

For the treatment of hypersensitive teeth and for the sealing of dentinal tubules for cavity preparations. Helps prevent cavities.

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 80022817

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.

List in the official revision dated 6 January 2026 (register: Licensed Natural Health Products Database (LNHPD), Health Canada: licensed products, ingredients, doses, uses and risks).

Has the product changed? Photograph the packaging.