Butler Fluoride Neutral Foam
Natural health product licensed in Canada
- Licence holder
- Sunstar Americas Inc.
- NPN or DIN-HM
- 02238605
- Status
- Inactive licence
- Licence date
- 20 December 2007
- Revision date
- Not provided
- Form
- Vaporisateur
- Route of administration
- Dentaire
- Application type
- DIN de transition
Oral dose analysis does not apply without an established exclusively oral route.
Composition
Medicinal composition not provided.
Non-medicinal ingredients
Eau purifiée, Parahydroxybenzoate de méthyle, Benzoate de sodium, Pluronic F87 USP, Poly(sorbate) 20, sulfate sodique de lauryle, Saveur de menthe, Glycérine, Sodium Saccharin, Phosphate de potassium, dibasique, Acide phosphorique
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Adultes | minimum: 6 years | 1 Pulvérisateur | Not specified |
| Enfants | maximum: 6 years | Not specified | Not specified |
Uses authorised in Canada
For topical application to aid in the protection against dental caries. This neutral pH product is recommended for patients having composite resin of procelain-type restorations, which could be damaged by APF treatment procedures.
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 02238605
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.