CompoAtlas

ZOSTRIX HP

Natural health product licensed in Canada

Licence holder
Bausch & Lomb Inc.
NPN or DIN-HM
02004240
Status
Active licence
Licence date
2 April 2008
Revision date
18 March 2025
Form
Crème
Route of administration
Topique
Application type
DIN de transition

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

Composition

Medicinal composition not provided.

Non-medicinal ingredients

Eau purifiée, Myristate d'isopropyle, Monostéarate de glycéryle, Alcool cétylique, alcool benzylique, Sorbitol, Petrolatum, White

PopulationAgeQuantity per servingFrequency
Adultesminimum: 18 yearsminimum: 1 Crèmeminimum: 3 Tous les jours ; maximum: 4 Tous les jours

Uses authorised in Canada

Used for the (temporary) relief of muscle and joint pain associated with rheumatoid arthritis or osteoarthritis, and pain of tendons and ligaments. Used to relieve skin (cutaneous) pain associated with conditions such as post-herpetic neuralgia and/or diabetic neuropathy.

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 02004240

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).

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