CompoAtlas

Probiorinse (TM)

Natural health product licensed in Canada

Licence holder
Probionase Therapies Inc. / Thérapies Probionase Inc.
NPN or DIN-HM
80085895
Status
Active licence
Licence date
6 June 2018
Revision date
Not provided
Form
Poudre pour solution
Route of administration
Nasale
Application type
Non traditionnelle

Oral dose analysis does not apply without an established exclusively oral route.

Composition

Medicinal ingredient and sourcePer dosage unit, according to the source
Sel de sodium d'acide carbonique (1:1)

Source : Bicarbonate de sodium

710 mg
Chlorure de sodium

Source : Chlorure de sodium

2,130 mg
Lactococcus lactis

Source : Cellule entière

2.4 Milliards d'UFC
Lactococcus lactis

Source : W136

2.4 Milliards d'UFC

Non-medicinal ingredients

Stéarate de magnésium, Maltodextrine

PopulationAgeQuantity per servingFrequency
Adultes et adolescentsminimum: 15 years1 Milliards d'UFC2 days

Uses authorised in Canada

Text supplied in English because no French text is available.

For temporary relief of nasal congestion, irritation and post-nasal drip. For quick relief of dry nasal passages due to Nasal allergies, Dryness and Hay Fever. May temporarily help control symptoms of chronic sinusitis.

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 80085895

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.

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