Butler Prophy Paste
Natural health product licensed in Canada
- Licence holder
- Sunstar Americas Inc.
- NPN or DIN-HM
- 02229505
- Status
- Inactive licence
- Licence date
- 20 December 2007
- Revision date
- Not provided
- Form
- Pâte
- 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
Silica, Dental-Type NF, D&C Red #28, FD & C Bleu 1 Lake, Red #22, Saveur de cerise, Glycérine, Terre de diatomées, Dioxyde de titane, Sodium silicate, Agar, Bubblegum flavour (artificial), Edetate Calcium Disodium, ponce, Sodium Saccharin, Saveur de menthe poivrée, Eau, Jaune D & C No. 10, Vanille (de Tahiti), Phosphate de sodium
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Sous-population S/O | Not specified | 250 millilitre | Not specified |
Uses authorised in Canada
Butler Prophy Paste is specifically disigned for polishing procedures as administered by licenced dental professionals. It consists of a unique mixture of polishing and cleansing agents and is supplied in the following grits. Fine: Minimal stain and polishing needs. Medium: Normal polishing and cleaning indicated. Coarse: Moderate to heavy stain removal. Plus*: Extremely heavy stain removal. For cleaning and polishing procedures as part of a professional prophylaxis procedure. (*not available in Canada)
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 02229505
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.