CompoAtlas

Feverfew 125 mg

Natural health product licensed in Canada

Licence holder
WN Pharmaceuticals Ltd
NPN or DIN-HM
80000200
Status
Active licence
Licence date
2 December 2004
Revision date
Not provided
Form
Caplet
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
Tanacetum parthenium125 mgNot calculated

Non-medicinal ingredients

Dioxyde de silicium, Stéarate de magnésium, Acide stéarique, Dihydrate dibasique de phosphate de calcium, Cellulose - microcrystalline

PopulationAgeQuantity per servingFrequency
AdultesNot specifiedminimum: 1 Caplet ; maximum: 2 CapletNot specified

Uses authorised in Canada

Traditionally used to help reduce the severity and/or frequency of migraine headaches and associated nausea and vomiting.

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 80000200

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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