ProCardiol
Food supplement declared in France, declaration No 2020-3-136, decision dated 4 March 2020
ProCardiol 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). 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
- DUOLIFE S.A.
- 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
- Capsule
- Daily dose
- 1-2 capsules
- Intended populations
- Homme, Femme
- Not recommended for (according to the manufacturer)
- Femmes allaitantes, Enfants (moins de 12 ans), Femmes enceintes
- Objectives stated by the manufacturer (these are not authorised claims)
- Antioxydant, Artères et cholestérol
Declaration 167813, 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
Leonurus cardiaca L.: L'étiquetage doit comporter un avertissement déconseillant l'emploi chez les femmes enceintes
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.
Declared composition
Plants
| Plant | Part | Preparation | Per day |
|---|---|---|---|
| Crataegus laevigata (Poir.) DC. | Fruit | Extrait sec aqueux | 160 mg |
| Vitis vinifera L. | Fruit (écorce) | Extrait sec aqueux | 138 mg |
| Hibiscus sabdariffa L. | Fleur | Extrait sec aqueux | 120 mg |
| Punica granatum L. | Fruit | Extrait sec aqueux | 100 mg |
| Aronia melanocarpa (michx.) Elliot | Fruit | Extrait sec aqueux | 60 mg |
| Leonurus cardiaca L. | Parties aériennes | Extrait sec aqueux | 40 mg |
| Scutellaria baicalensis Georgi | Racine | Extrait sec aqueux | 40 mg |
| Cynara scolymus L. | Feuille | Extrait sec aqueux | 21 mg |
| Olea europaea L. | Fruit | Extrait sec aqueux | 21 mg |
Other active ingredients
| Name | Per day |
|---|---|
| Inuline | not declared |
Vitamins and minerals
Compl'Alim does not publish vitamin and mineral doses. The references below help you read the product label: EFSAEuropean Food Safety Authority. safety limit for adults and maximum dose set in France per product (Order of 9 May 2006, not revised since November 2006).
| Declared form | Nutrient | EFSA limit, adults | Maximum dose in France |
|---|---|---|---|
| Dioxyde de silicium | Silicium | pas de limite (données insuffisantes) | aucune dose fixée |
Additives
Hydroxypropyl Méthyl Cellulose, E418, E141
List from the declaration, administrative decision dated (Compl'Alim, food supplement declarations (France)).
List recorded in 2020. Photograph the packaging to check whether it has changed.
Has the product changed? Photograph the packaging.
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.