CompoAtlas

ACTYFILUS

Food supplement declared in France, declaration No 2024-9-243, decision dated 4 September 2024

ACTYFILUS 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
LABORATOIRE DENEL
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
1 à 3 gélule(s)
Objectives stated by the manufacturer (these are not authorised claims)
Immunité

Declaration 308982, 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
Inulinenot declared

Micro-organisms

StrainPer day
Lactobacillus Rhamnosus GG30,000,000,000 (unit not declared)
Bifidobacterium Lactis DSM 15954 & Bl-048,999,999,000 (unit not declared)
Lactobacillus Acidophilus La-56,000,000,000 (unit 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 formNutrientEFSA limit, adults Maximum dose in France
CholécalciférolVitamine D100 µg (4,000 UI)5 µg (200 UI)

Additives

E470b

Other ingredients

maltodextrine, Gélule végétale

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Label warnings

Les femmes enceintes ou allaitantes doivent consulter un professionnel de santé avant toute complémentation

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.

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