Fluorinse 0.05%
Natural health product licensed in Canada
- Licence holder
- Procter & Gamble Inc.
- NPN or DIN-HM
- 00782890
- Status
- Active licence
- Licence date
- 30 June 2008
- Revision date
- Not provided
- Form
- Produit de rinçage
- Route of administration
- Dentaire
- Application type
- DIN de transition
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 | 0.05 % (p/p) |
Non-medicinal ingredients
(p)-hydroxybenzoate de méthyle, Eau, Huile de menthe poivrée, Poloxamer, Anis, FD & C Bleu 1 Lake, Propyl paraben, Glycérine, Alcool éthylique, Sodium Phosphate, Dibasic (dihydrate), Menthol, Spearmint oil, EDTA de sodium
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Enfants | minimum: 6 years | minimum: 10 mL ; maximum: 15 mL | 1 Tous les jours |
| Adultes | Not specified | minimum: 10 mL ; maximum: 15 mL | 1 Tous les jours |
Uses authorised in Canada
Fights cavities. Anti-cavity. Anti-cavity.
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
Do not swallow. Keep out of reach of children. Protect from freezing. Do not use if safety seal is broken or missing.
Source
Official Health Canada record, licence 00782890
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.