asonor

Natural health product licensed in Canada

Licence holder

TannerMedico A/S

NPN or DIN-HM

80042277

Status

Active licence

Licence date

14 May 2013

Revision date

9 September 2013

Form

Solution

Route of administration

Nasale

Application type

Non traditionnelle

Composition

Medicinal composition not provided.

Non-medicinal ingredients

Eau purifiée, EDTA de sodium, Sorbate de potassium, Glycérol, Poly(sorbate) 80

Recommended doses in Canada

Uses authorised in Canada

For the temporary relief of snoring by lubricating and softening of nasal mucous membrane/nasal passage.

A use authorised in Canada is not an authorised health claim in the European Union. See the health claims register.

Warnings in Canada

• Précautions et mises en garde

  Keep out of reach of children. Do not share the device with anyone else. Do not swallow. Consult a health practitioner if symptoms persist or worsen, if the discharge is persistently thick and yellow or green, or if the skin at the base of the nostrils becomes raw or crusted. Consult a healthcare practitioner before use if you have asthma or other chronic respiratory complaints.

Source

Official Health Canada record, licence 80042277

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 9 September 2013 (register: Licensed Natural Health Products Database (LNHPD), Health Canada: licensed products, ingredients, doses, uses and risks).

List recorded in 2013. Photograph the packaging to check whether it has changed.

Has the product changed? Photograph the packaging.