GINKGO BILOBA
Food supplement declared in France, declaration No 2018-6-935
GINKGO BILOBA is a food supplement declared in France. Status: retiré du marché le 1 June 2024. 1 rule of use applies to its ingredients (limits and warnings).
- Brand
- not provided
- Food business operator placing the product on the market
- LABORATOIRE MARQUE VERTE
- Status
- Retiré du marché le 1 June 2024
- Form
- Gélule
- Daily dose
- 1 gélule par jour
- Directions for use
- Prendre 1 gélule par jour avec un grand verre d'eau.
- Not recommended for (according to the manufacturer)
- Femmes allaitantes, Femmes enceintes, Sous anticoagulants, Sous antidépresseurs
- Objectives stated by the manufacturer (these are not authorised claims)
- Mémoire
Declaration 289544, procedure Article 15. Compl'Alim, food supplement declarations (France), retrieved 23 October 2026.
Regulatory points
- Conditions légales
Ginkgo biloba L.: L'étiquetage des compléments alimentaires qui contiennent la feuille de la plante Ginkgo biloba L. doit comporter un avertissement avec la teneur suivante: "Consultez votre médecin en cas de prise simultanée d'anticoagulants."
Source: French orders of 9 May 2006 (nutrients), 24 June 2014 (plants) and 26 September 2016 (other substances), consolidated LEGI collection, arrêté du 24 juin 2014, annexe I.
- Information
Retiré du marché le 1 June 2024, according to Compl'Alim.
Source: Compl'Alim, food supplement declarations (France).
Declared composition
Plants
| Plant | Part | Preparation | Per day |
|---|---|---|---|
| Ginkgo biloba L. | Feuille | Extrait sec hydroalcoolique | 80 mg |
| Ginkgo biloba L. | Feuille | Poudre (de plantes séchées ou broyées) | 50 mg |
Additives
E470b, E464
Other ingredients
maltodextrine
The evidence date of this ingredient list is unknown.
Has the product changed? Photograph the packaging.
Label warnings
Consultez votre médecin en cas de prise simultanée d'anticoagulants. Déconseillé chez les femmes enceintes et allaitantes, ainsi que chez les personnes sous antidépresseurs.
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.
Other declarations with the same name
This name is used by more than 10 declarations from different companies, so it does not identify one product. See every declaration with this name.