Ultracare

Natural health product licensed in Canada

Licence holder

Ultradent Products Inc.

NPN or DIN-HM

00791474

Status

Active licence

Licence date

20 August 2009

Revision date

30 July 2012

Form

Gel

Route of administration

Dentaire

Application type

DIN de transition

Composition

Medicinal composition not provided.

Non-medicinal ingredients

Saveur de fraise, Sodium Saccharin, Glycérine, Aspartame, Éthanol, Dioxyde de titane, D&C Red #28, Amaretto flavor, FD & C Rouge # 40, Bubblegum flavour, Poly(éthylène glycol)

Recommended doses in Canada

Uses authorised in Canada

Text supplied in English because no French text is available.

Topical anesthetic. For the temporary relief of occasional minor irritation and pain, associated with: minor dental procedures, sore mouth and throat, minor injury of the gums, canker sores, minor irritation of the mouth or gums caused by dentures or orthodontic appliances.

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 00791474

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.

List in the official revision dated 30 July 2012 (register: Licensed Natural Health Products Database (LNHPD), Health Canada: licensed products, ingredients, doses, uses and risks).

List recorded in 2012. Photograph the packaging to check whether it has changed. Photograph the packaging