CompoAtlas

Probaclac E

Probaclac E, licence 80069647: 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

Licence holder
Les laboratoires Nicar inc.
NPN or DIN-HM
80069647
Status
Inactive licence
Licence date
24 May 2016
Revision date
22 December 2020
Form
Comprimé
Route of administration
Orale
Application type
Officinale

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 sourcePer dosage unit, according to the sourceMaximum per day, adult
Bifidobacterium breve

Source : Bifidobacterium breve A055

300.0 %Not calculated
Bifidobacterium breve

Source : Cellule entière

300.0 %Not calculated
Bifidobacterium breve

Source : Bifidobacterium breve A055

338.0 Milliards d'UFCNot calculated
Bifidobacterium breve

Source : Cellule entière

338.0 Milliards d'UFCNot calculated
Bifidobacterium longum subsp. longum

Source : Bifidobacterium longum subsp. longum A027

300.0 %Not calculated
Bifidobacterium longum subsp. longum

Source : Cellule entière

300.0 %Not calculated
Bifidobacterium longum subsp. longum

Source : Bifidobacterium longum subsp. longum A027

113.0 Milliards d'UFCNot calculated
Bifidobacterium longum subsp. longum

Source : Cellule entière

113.0 Milliards d'UFCNot calculated

Non-medicinal ingredients

Sucrose, Acide ascorbique, Cellulose microcristalline, Sorbitol, Maltodextrine, Anthocyanines, Stéarate de magnésium, Saveur de raisin, Betterave rouge, Inuline, Amidon de maïs, Acide citrique, Dioxyde de silicium

PopulationAgeQuantity per servingFrequency
Enfants et Adolescentsminimum: 3.0 Année(s)minimum: 1.0 Comprimé2.0 Tous les jours

Uses authorised in Canada

Contribue à soutenir la santé intestinale/gastrointestinal.

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 80069647

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 2020. Photograph the packaging to check whether it has changed.

Has the product changed? Photograph the packaging.

List recorded in 2020. Photograph the packaging to check whether it has changed.

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