Canadian Ginseng
Food supplement declared in France, declaration No 2017-3-633, decision dated 15 March 2017
Canadian Ginseng is a food supplement declared in France. Status: déclaré en France, commercialisation possible : l'administration ne s'est pas opposée à la déclaration (ce n'est ni une autorisation ni une évaluation de sécurité). 1 point in its composition requires a check (prohibited substance, dose or novel food).
- Brand
- not provided
- Food business operator placing the product on the market
- PROMEDICA Pharmaservice GmbH
- Status
- Déclaré en France, commercialisation possible : l'administration ne s'est pas opposée à la déclaration (ce n'est ni une autorisation ni une évaluation de sécurité)
- Form
- Gélule
- Daily dose
- 4 gélules
- Directions for use
- 2 gélules 2 fois par jour avec un verre d'eau
- Not recommended for (according to the manufacturer)
- Sous antidiabétiques
Declaration 279659, procedure Article 15. Compl'Alim, food supplement declarations (France), retrieved 23 October 2026.
Regulatory points
- À vérifier
The composition lists additive E171 (titanium dioxide), removed from the list of additives allowed in food, supplements included: since 7 August 2022, a supplement containing it can no longer be placed on the market in the Union. The declaration predates this removal: if the product is still sold, its formula must have changed; check the label.
Source: Regulation (EU) 2022/63: titanium dioxide (E171) removed from the food additives allowed in the EU, règlement (UE) 2022/63.
Declared composition
Plants
| Plant | Part | Preparation | Per day |
|---|---|---|---|
| Panax quinquefolius L. | Racine | Poudre (de plantes séchées ou broyées) | 800 mg |
Additives
E464, E171, E172
List from the declaration, administrative decision dated (Compl'Alim, food supplement declarations (France)).
List recorded in 2017. Photograph the packaging to check whether it has changed. Photograph the packaging
Label warnings
Déconseillé aux personnes sous traitement antidiabétique
This information reproduces the manufacturer's declaration to the administration (DGAL). It does not say whether the product is effective and does not replace advice from a doctor or pharmacist, particularly during pregnancy or when taking medication.