CompoAtlas

Luffeel

Luffeel, licence 80025163: active licence in Health Canada data. The French and European references below do not constitute authorisation for sale in France or an assessment of safety or efficacy.

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)

Natural health product licensed in Canada

Licence holder
Biologische Heilmittel Heel GmbH
NPN or DIN-HM
80025163
Status
Active licence
Licence date
4 May 2011
Revision date
12 June 2013
Form
Pulvérisateur nasal (solution)
Route of administration
Nasale
Application type
Homéopathique

If this product were sold in France

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
Luffa operculata

Source : Fruit séché

Potency : 10.0 g D 12

12.0 DNot calculated
Galphimia glauca

Source : Feuilles & inflorescences séchées

Potency : 10.0 g D 30

30.0 DNot calculated
Histaminum

Source : Histamine

Potency : 5.0 g D 12

12.0 DNot calculated
Histaminum

Source : Histamine

Potency : 5.0 g D 30

30.0 DNot calculated
Luffa operculata

Source : Fruit séché

Potency : 10.0 g D 4

4.0 DNot calculated

Non-medicinal ingredients

Sodium Phosphate, Dibasic (dihydrate), Eau purifiée, Chlorure de sodium, Benzalkonium chloride solution, phosphate monobasique de sodium (dihydrate)

PopulationAgeQuantity per servingFrequency
Adultesminimum: 12.0 Année(s)minimum: 1.0 Pulvérisateur ; maximum: 2.0 Pulvérisateurmaximum: 6.0 Tous les jours
Adultesminimum: 12.0 Année(s)minimum: 1.0 Pulvérisateur ; maximum: 2.0 Pulvérisateurminimum: 3.0 Tous les jours ; maximum: 5.0 Tous les jours

Uses authorised in Canada

Text supplied in English because no French text is available.

Homeopathic preparation used for the treatment of hay fever.

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

Warnings in Canada

No French warning text available in the imported data.

Warnings are available in English on the official record.

Source

Official Health Canada record, licence 80025163

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 2013. Photograph the packaging to check whether it has changed.

Has the product changed? Photograph the packaging.

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

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