PeriActive
PeriActive, licence 80070423: active licence in Health Canada data. The French and European references below do not constitute authorisation for sale in France or an assessment of safety or efficacy.
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)
Natural health product licensed in Canada
- Licence holder
- Izun Pharmaceaticals Corp.
- NPN or DIN-HM
- 80070423
- Status
- Active licence
- Licence date
- 17 June 2016
- Revision date
- Not provided
- Form
- Liquide
- Route of administration
- Orale
- Application type
- Non traditionnelle
If this product were sold in France
No point flagged by the rules we apply.
A daily quantity is calculated only for an explicit adult oral dosage, stated per day and in a solid unit matching the product form. Ambiguous units, liquids, powders and paediatric doses are not extrapolated. A quantity not calculated is not compared with dose limits. This analysis does not constitute authorisation for sale in France or an assessment of safety or efficacy.
Composition
| Medicinal ingredient and source | Per dosage unit, according to the source | Maximum per day, adult |
|---|---|---|
| Echinacea purpurea Source : Racine Extract : Matériel brut sec Extraction ratio : 8.0:1.0 Dry plant equivalent : 14.8 milligramme | 1.85 milligramme | Not calculated |
| Centella asiatica Source : Feuille Extract : Matériel brut sec Extraction ratio : 6.0:1.0 Dry plant equivalent : 22.2 milligramme | 3.7 milligramme | Not calculated |
| Sambucus nigra subsp. nigra Source : Fleur Extract : Matériel brut sec Extraction ratio : 7.0:1.0 Dry plant equivalent : 220.5 milligramme | 31.5 milligramme | Not calculated |
Non-medicinal ingredients
Chlorure de cétylpyridinium, Saveur de menthe, EDTA de sodium, Acide D-lactique, Sorbitol, Saveur de cannelle, Bleu FD&C n° 1, Propylène glycol, Benzoate de sodium, Eau, Sucralose, Maltodextrine, Menthol, Huile de ricin hydrogénée de PEG-40
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Adultes et adolescents | minimum: 13.0 Année(s) | 3.0 Cuillère à thé ; minimum: 3.0 Cuillère à thé ; maximum: 3.0 Cuillère à thé | 2.0 Tous les jours ; maximum: 2.0 Tous les jours |
| Adolescentes | minimum: 9.0 Année(s) ; maximum: 12.0 Année(s) | 2.0 Cuillère à thé ; minimum: 2.0 Cuillère à thé ; maximum: 2.0 Cuillère à thé | 2.0 Tous les jours ; maximum: 2.0 Tous les jours |
Uses authorised in Canada
Reduces inflammation and control gingivitis. Promotes gingival healing. Reduces plaque build-up. Reduce irritation and bleeding associated with gingivitis. Helps reduce oral bacteria for the maintenance of good oral hygiene.
A use authorised in Canada is not an authorised health claim in the European Union. See the health claims register.
Warnings in Canada
- Précautions et mises en garde
Speak with a health professional if you are pregnant or breastfeeding.
Source
Official Health Canada record, licence 80070423
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.