CompoAtlas

Ginger Tablets

Ginger Tablets, licence 80092037: 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

Other names
Anti-nauseant Tablets, Comprimés Anti-Nausée, Gingembre
Licence holder
Wampole Group L.P.
NPN or DIN-HM
80092037
Status
Active licence
Licence date
3 May 2019
Revision date
26 October 2024
Form
Comprimé
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
Zingiber officinale

Source : Rhizome

Extract : Matériel brut sec

Extraction ratio : 25.0:1.0

Dry plant equivalent : 500.0 milligramme

20.0 milligrammeNot calculated

Non-medicinal ingredients

Laque d'aluminium jaune FD&C No. 5, Hypromellose, Maltodextrine, Laque d'aluminium jaune FD&C No. 6, Cellulose microcristalline, Talc, Poly(dextrose), Dioxyde de titane, Dioxyde de silicium, Macrogol 4000, Croscarmellose de sodium, Stéarate de magnésium, Poly(alcool vinylique)

PopulationAgeQuantity per servingFrequency
Adolescentesminimum: 12.0 Année(s) ; maximum: 17.0 Année(s)minimum: 1.0 Comprimé ; maximum: 2.0 Compriméminimum: 1.0 Tous les jours ; maximum: 3.0 Tous les jours
Adultesminimum: 18.0 Année(s)minimum: 1.0 Comprimé ; maximum: 2.0 Compriméminimum: 1.0 Tous les jours ; maximum: 3.0 Tous les jours
Enfantsminimum: 6.0 Année(s) ; maximum: 11.0 Année(s)minimum: 1.0 Comprimé ; maximum: 2.0 Compriméminimum: 1.0 Tous les jours ; maximum: 3.0 Tous les jours

Uses authorised in Canada

Help(s) prevent nausea and vomiting associated with motion sickness, and/or seasickness. Traditionally used in Herbal Medicine as an expectorant and cough suppressant (antitussive) to help relieve bronchitis as well as coughs and colds. Traditionally used in Herbal Medicine to help relieve digestive upset/disturbances including lack of appetite, nausea, digestive spasms, indigestion, dyspepsia and flatulent colic (carminative).

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 80092037

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 2024. Photograph the packaging to check whether it has changed.

Has the product changed? Photograph the packaging.

List recorded in 2024. Photograph the packaging to check whether it has changed.

Enter to analyse, Shift+Enter for a new line