CompoAtlas

PERNAFLEX

Food supplement declared in France, declaration No 2024-5-1471, decision dated 29 May 2024

PERNAFLEX 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). None of the rules we check flags an issue with its declared composition; vitamin and mineral doses are not published by Compl'Alim and are therefore not checked.

Brand
not provided
Food business operator placing the product on the market
SEKOYA EUROPE
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 par jour
Objectives stated by the manufacturer (these are not authorised claims)
Antioxydant, Articulations

Declaration 273063, procedure Article 15. Compl'Alim, food supplement declarations (France), retrieved 23 October 2026.

Regulatory points

None of the rules we check applies to the declared ingredients.

Declared composition

Other active ingredients

NamePer day
Perna canaliculusnot declared
Glucosamine sulfate 2 KClnot declared
Sulfate de chondroïtinenot 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 formNutrientEFSA limit, adults Maximum dose in France
Citrate de cuivreCuivre5,000 µg2,000 µg
Citrate de manganèseManganèse8 mg (niveau de sécurité)3.5 mg
L-sélénométhionineSélénium255 µg50 µg
Acide L-ascorbiqueVitamine Cpas de limite (données insuffisantes)180 mg
Mélange de tocophérolsVitamine E300 mg30 mg
Citrate de zincZinc25 mg15 mg

Additives

Hydroxypropyl Méthyl Cellulose

List from the declaration, administrative decision dated (Compl'Alim, food supplement declarations (France)).

List recorded in 2024. Photograph the packaging to check whether it has changed. Photograph the packaging

Label warnings

Si vous êtes enceinte ou allaitante, ou traité par anti-vitamine K, demandez l’avis de votre médecin avant d’utiliser ce produit.

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.

List recorded in 2024. Photograph the packaging to check whether it has changed.

Enter to analyse, Shift+Enter for a new line