NaFrinse Unit Dose Fluoride Solution
Natural health product licensed in Canada
- Licence holder
- Medical Products Laboratories, Inc
- NPN or DIN-HM
- 80024502
- Status
- Inactive licence
- Licence date
- 4 April 2011
- Revision date
- Not provided
- Form
- Liquide
- Route of administration
- Dentaire
- Application type
- Non traditionnelle
Oral dose analysis does not apply without an established exclusively oral route.
Composition
Medicinal composition not provided.
Non-medicinal ingredients
Bubblegum flavour (artificial), Saveur de menthe, Saveur artificielle de cerise, Brown Dye, FD&C Blue Dye #1, D&C Red #33, Saccharinate de sodium, Saveur de raisin, Saveur d'orange, Eau purifiée, Acide citrique, Artificial Root Beer Flavor, FD&C Yellow No. 5, Sorbate de potassium, FD&C Yellow 6
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Enfants | minimum: 6 years | 10 mL | 1 Toutes les semaines |
Uses authorised in Canada
Text supplied in English because no French text is available.
NaFrinse, containing sodium fluoride is indicated as a dental rinse for the prevention of dental caries in children.
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 80024502
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.