ZINUTRIK
Food supplement declared in France, declaration No 2018-3-363
ZINUTRIK is a food supplement declared in France. Status: retiré du marché le 6 June 2025. 2 points in its composition require a check (prohibited substance, dose or novel food). 1 rule of use applies to its ingredients (limits and warnings).
- Brand
- not provided
- Food business operator placing the product on the market
- SA
- Status
- Retiré du marché le 6 June 2025
- Form
- Comprimé
- Daily dose
- 1
- Directions for use
- un comprimé par jour à avaler avec de l'eau, de préfétence le matin
- Not recommended for (according to the manufacturer)
- Femmes allaitantes, Femmes enceintes
- Objectives stated by the manufacturer (these are not authorised claims)
- Antioxydant, Détoxifiant / Draineur
- Flavourings
- non
Declaration 153659, procedure Article 15. Compl'Alim, food supplement declarations (France), retrieved 23 October 2026.
Regulatory points
- À vérifier
Scutellaria baicalensis Georgi (zie ook lijst 3/voir aussi liste 3): dangerous plant prohibited in food in Belgium (list 1). L’utilisation de la racine provenant de cette plante est autorisée dans les denrées alimentaires. List 3 also covers Scutellaria baicalensis Georgi, parts: feuille, racine. Check the plant part used, the preparation, the conditions and the product notification.
Source: Belgium, Royal Decree of 31 August 2021, plant lists (annex replaced on 30 January 2024), arrêté royal du 31 août 2021, annexe remplacée le 30 janvier 2024, liste 1, page PDF 82 ; liste 3, pages PDF 251.
- À vérifier
Scutellaria spp.: dangerous plant prohibited in food in Belgium (list 1). The entire genus Scutellaria is listed. List 3 also covers Scutellaria baicalensis Georgi, parts: feuille, racine. Check the plant part used, the preparation, the conditions and the product notification.
Source: Belgium, Royal Decree of 31 August 2021, plant lists (annex replaced on 30 January 2024), arrêté royal du 31 août 2021, annexe remplacée le 30 janvier 2024, liste 1, page PDF 83 ; liste 3, pages PDF 251.
- 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 6 June 2025, according to Compl'Alim.
Source: Compl'Alim, food supplement declarations (France).
Declared composition
Plants
| Plant | Part | Preparation | Per day |
|---|---|---|---|
| Ginkgo biloba L. | Feuille | Extrait fluide hydroalcoolique | 250 mg |
| Scutellaria baicalensis Georgi | Racine | Extrait fluide hydroalcoolique | 166.7 mg |
| Coffea arabica L. | Graine | Extrait sec hydroalcoolique | 100 mg |
Other active ingredients
| Name | Per day |
|---|---|
| Rutine | not declared |
Additives
E460, E463, E341, E553b, E470b, E551
Other ingredients
maltodextrine
The evidence date of this ingredient list is unknown.
Has the product changed? Photograph the packaging.
Label warnings
Si vous prenez des anticoagulants ou des anti agrégants , consultez votre médecin
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
In France, every company that markets a supplement declares it, so one product can have several declarations (new formula, another distributor, an older declaration withdrawn). Each line compares the declared composition with this page.