Curcuflex
Food supplement declared in France, declaration No 2020-9-1154
Curcuflex (Dexsil) is a food supplement declared in France. Status: retiré du marché le 2 July 2023. 1 rule of use applies to its ingredients (limits and warnings).
- Brand
- Dexsil
- Food business operator placing the product on the market
- BIOXYDIET FRANCE SAS
- Status
- Retiré du marché le 2 July 2023
- Form
- Autre : Bouteille
- Daily dose
- 15 ml
- Directions for use
- Prendre le matin à jeun. Prendre 15 ml/jour pendant 3 mois, renouvelable au besoin.
- Not recommended for (according to the manufacturer)
- Sous anticoagulants
- Objectives stated by the manufacturer (these are not authorised claims)
- Articulations
Declaration 305271, procedure Article 15. Compl'Alim, food supplement declarations (France), retrieved 23 October 2026.
Regulatory points
- Conditions légales
Urtica dioica L.: L'étiquetage des compléments alimentaires contenant les parties souterraines de cette plante doit comporter une mention recommandant de prendre conseil auprès d'un professionnel de santé ("Demander l'avis de votre médecin et /ou pharmacien").
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 2 July 2023, according to Compl'Alim.
Source: Compl'Alim, food supplement declarations (France).
Declared composition
Plants
| Plant | Part | Preparation | Per day |
|---|---|---|---|
| Urtica dioica L. | Feuille | Extrait fluide hydroalcoolique | 1.125 mg |
| Citrus maxima (Burm.) Merr. | Fruit | Extrait sec hydroglycériné | 0.6 mg |
Other active ingredients
| Name | Per day |
|---|---|
| Gamma-cyclodextrine | not declared |
| Curcumine | 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 |
|---|---|---|---|
| Gluconate de cuivre | Cuivre | 5,000 µg | 2,000 µg |
| Acide silicique | Silicium | pas de limite (données insuffisantes) | aucune dose fixée |
| Bisglycinate de zinc | Zinc | 25 mg | 15 mg |
Additives
E967, E338, E415, E412, E955, E960
Other ingredients
Eau purifiée
The evidence date of this ingredient list is unknown.
Has the product changed? Photograph the packaging.
Label warnings
Déconseillé aux personnes sous anticoagulants.
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.
- CURCUFLEX Dexsil, declared in 2024 : same declared composition
- Curcuflex Dexsil, declared in 2020, withdrawn from the market : different composition: 7 ingredient(s) added, 14 missing
Brand : Dexsil