Orajel Toothache Maximum Strength Gel
Natural health product licensed in Canada
- Licence holder
- Church & Dwight Canada Corp.
- NPN or DIN-HM
- 80091462
- Status
- Active licence
- Licence date
- 22 March 2019
- Revision date
- Not provided
- Form
- Gel
- Route of administration
- Dentaire
- Application type
- Non traditionnelle
Oral dose analysis does not apply without an established exclusively oral route.
Composition
| Medicinal ingredient and source | Per dosage unit, according to the source |
|---|---|
| Chlorure de zinc (ZnCl2) Source : Chlorure de zinc | 0.15 % |
Non-medicinal ingredients
Glycyrrhizinate d'ammonium, Saveur, Acide sorbique, Sacharinate de sodium, Eau, Poly(éthylène glycol)
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Adultes | minimum: 19 years | 1 Gel | minimum: 1 Tous les jours ; maximum: 4 Tous les jours |
Uses authorised in Canada
For the temporary relief of pain arising as a result of toothache. An oral astringent. For the temporary relief of pain due to minor irritation or injury of the mouth and gums.
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 80091462
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.