CompoAtlas

DONA®

Natural health product licensed in Canada

Other names
DONA® Crystalline Glucosamine Sulfate
Licence holder
Auro Pharma Inc.
NPN or DIN-HM
80096645
Status
Active licence
Licence date
15 January 2020
Revision date
12 April 2022
Form
Comprimé, enrobé par pellicule
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
Sulfate de 2-Amino-2-désoxy-D-glucose

Source : Exosquelette de crabe

750 mgNot calculated
Sulfate de 2-Amino-2-désoxy-D-glucose

Source : Exosquelette de crevette

750 mgNot calculated

Non-medicinal ingredients

NA, Talc, Maltodextrine, Poly(dextrose), Macrogol 6 000, Croscarmellose de sodium, Stéarate de magnésium, Cellulose microcristalline, Polyvinylpyrrolidone, Hypromellose, Dioxyde de titane

PopulationAgeQuantity per servingFrequency
Adultesminimum: 18 years2 Comprimé1 Tous les jours

Uses authorised in Canada

A factor in maintaining good cartilage and/or joint health. Helps protect against the deterioration of cartilage and relieve joint pain associated with osteoarthritis. Helps to protect against the deterioration of cartilage. Helps to relieve joint pain associated with osteoarthritis. Helps to relieve pain associated with osteoarthritis of the knee.

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 80096645

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.

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 2022. Photograph the packaging to check whether it has changed. Photograph the packaging

List recorded in 2022. Photograph the packaging to check whether it has changed.

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