CompoAtlas

Cholasyn Plus

Cholasyn Plus, licence 02241040: inactive 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

Other names
Laxatif
Licence holder
Fabrication JAMP Pharma Inc. / JAMP Manufacturing Inc.
NPN or DIN-HM
02241040
Status
Inactive licence
Licence date
20 December 2007
Revision date
9 May 2018
Form
Comprimé
Route of administration
Orale
Application type
DIN de transition

If this product were sold in France

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 sourcePer dosage unit, according to the sourceMaximum per day, adult
Cascara sagrada

Source : Écorce

3.34 mgNot calculated
Sennoside A&B

Source : Feuille(s)

12.0 mgNot calculated

Non-medicinal ingredients

Croscarmellose de sodium, Oléorésin capsicum, Cire de Carnauba, Polyethylene glycol 400, papaïne, Povidone, Cellulose, microcristalline, Alfalfa, Pancréatine, Stéarate de magnésium, Spectracell 15 FG

PopulationAgeQuantity per servingFrequency
AdultesNot specifiedminimum: 1.0 Comprimé ; maximum: 2.0 CompriméNot specified

Uses authorised in Canada

Les comprimés cholasyn plus apportent un soulagement efficace de la constipation occasionnelle en agissant directement sur le péristaltisme des intestins.

A use authorised in Canada is not an authorised health claim in the European Union. See the health claims register.

Warnings in Canada

Source

Official Health Canada record, licence 02241040

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).

List recorded in 2018. Photograph the packaging to check whether it has changed.

Has the product changed? Photograph the packaging.

List recorded in 2018. Photograph the packaging to check whether it has changed.

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