CompoAtlas

Genacol Instant

Natural health product licensed in Canada

Licence holder
Genacol Group Inc.
NPN or DIN-HM
80016498
Status
Active licence
Licence date
10 March 2010
Revision date
17 January 2017
Form
Gel
Route of administration
Topique
Application type
Officinale

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

Composition

Medicinal composition not provided.

Non-medicinal ingredients

Poly(sorbate) 20, Eau, Dioxyde de titane, Gomme de cellulose, Hydroxide de sodium, alcool benzylique, Hypromellose, Collagène hydrolysé, Acide Déshydroacétique, Glycérine, Mica, Éthanol, D-Mannitol, Extrait d'Aloe barbadensis, Oxydes de fer, Copolymère d'acrylates

PopulationAgeQuantity per servingFrequency
AdultesNot specifiedNot specifiedNot specified

Uses authorised in Canada

Utilisé traditionellement en phytothérapie pour aider à soulager la douleur et/ou l'inflammation des muscles et des articulations (e.g. les entorses, les ecchymoses, la douleur articulaire).

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 80016498

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 2017. Photograph the packaging to check whether it has changed. Photograph the packaging

List recorded in 2017. Photograph the packaging to check whether it has changed.

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