CompoAtlas

MaxRelief Pain Relief Spray

Natural health product licensed in Canada

Licence holder
MaxRelief USA, Inc.
NPN or DIN-HM
80089939
Status
Active licence
Licence date
7 January 2019
Revision date
Not provided
Form
Vaporisateur
Route of administration
Topique
Application type
Officinale

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

Composition

Medicinal ingredient and sourcePer dosage unit, according to the source
dl-Camphre

Source : dl-Camphre

3 Pour cent

Non-medicinal ingredients

Alcool dénaturé, Phénoxyéthanol, Huile d'émeu, Extrait de fleur d'Arnica montana, Extrait de fleur/ de feuilles/ de tige de Rosmarinus Officinalis (Romarin), Extrait de feuilles d'Eucalyptus globulus, Ethylhexylglycérine, Laureth-4, Myristate d'isopropyle, Hydroxyde de sodium, Acide citrique

PopulationAgeQuantity per servingFrequency
Adultes et enfantsminimum: 2 years1 Pulvérisateurminimum: 3 Tous les jours ; maximum: 4 Tous les jours

Uses authorised in Canada

Temporarily relieves aches and pains of muscles and joints associated with one or more of the following: Simple backache, lumbago, strains and sprains (involving muscles, tendons, and/or ligaments), and arthritis. For the temporary relief of back, neck and muscle pain, arthritis and joint pain.

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 80089939

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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