CompoAtlas

NaFrinse Sodium Fluoride Packets

Natural health product licensed in Canada

Other names
1 g NaF packets : 2.45g Powder, 2 g NaF packets : 4.90g Powder, 3 g NaF packets : 7.35g Powder
Licence holder
Medical Products Laboratories Inc.
NPN or DIN-HM
80025841
Status
Inactive licence
Licence date
17 June 2011
Revision date
Not provided
Form
Poudre
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

FD&C Yellow No. 5, FD&C Blue #1, Saveur de menthe poivrée, FD&C Yellow 6, Saveur d'orange, Saccharinate de sodium, Acide citrique, Saveur de raisin, Sorbate de potassium, Artificial Root Beer Flavor, D&C Red #33, Saveur de cerise, Bubblegum flavour (artificial)

PopulationAgeQuantity per servingFrequency
Enfantsminimum: 6 years10 mL1 week

Uses authorised in Canada

Text supplied in English because no French text is available.

NaFrinse, containing sodium fluoride is indicated as a dental rinse in children in the areas where the level of fluoride in drinking water is inadequate.

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 80025841

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.

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