CompoAtlas

Anbesol® Extra Strength Liquid

Natural health product licensed in Canada

Licence holder
Knight Therapeutics Inc.
NPN or DIN-HM
02237869
Status
Active licence
Licence date
3 December 2007
Revision date
1 May 2026
Form
Liquide
Route of administration
Topique
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

FD&C Blue #1, Sodium Saccharin, Jaune D & C No. 10, FD & C Red #40 Lake, Saveur, alcool benzylique, propylèneglycol, Polyethylene glycol 400, Parahydroxybenzoate de méthyle

PopulationAgeQuantity per servingFrequency
Adultes et enfantsminimum: 2 yearsNot specifiedminimum: 3 Tous les jours ; maximum: 4 Tous les jours

Uses authorised in Canada

Text supplied in English because no French text is available.

Topical anesthetic. For temporary pain relief of cold sores, canker sores, toothaches, denture irritation, sun and fever blisters and brace pain.

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 02237869

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 (register: Licensed Natural Health Products Database (LNHPD), Health Canada: licensed products, ingredients, doses, uses and risks).

Has the product changed? Photograph the packaging.

Enter to analyse, Shift+Enter for a new line