CompoAtlas

LUTEVAX MACULA PRO

Food supplement declared in France, declaration No 2022-5-274, decision dated 6 May 2022

LUTEVAX MACULA PRO 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
GRICAR CHEMICAL S.R.L.
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
Comprimé
Daily dose
2 comprimés et 1 gélule
Directions for use
un comprimé le matin et un comprimé le soir. Une gélule au déjeuner avec d'eau
Not recommended for (according to the manufacturer)
Adolescents (moins de 18 ans), Femmes allaitantes, Enfants (moins de 12 ans), Enfants en bas âge (1 à 3 ans), Femmes enceintes, Nourrissons (moins de 1 an), Sous antidépresseurs, Enfants (de moins de 6 ans), Enfants (de moins de 10 ans)
Objectives stated by the manufacturer (these are not authorised claims)
Système nerveux, Œil / Vision

Declaration 269591, 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

Plants

PlantPartPreparationPer day
Tagetes erecta L.FleurExtrait sec alcoolique200 mg
Coffea arabica L.GraineExtrait sec hydroalcoolique30 mg
Melissa officinalis L.FeuilleExtrait sec aqueux30 mg
Crocus sativus L.StigmatesExtrait sec alcoolique20 mg
Tagetes erecta L.FleurExtrait sec hydroalcoolique20 mg

Other active ingredients

NamePer day
Citicolinenot declared
Huile de poissonnot 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
Gluconate de cuivreCuivre5,000 µg2,000 µg
Acide L-ascorbiqueVitamine Cpas de limite (données insuffisantes)180 mg
Acétate de DL-alpha-tocophéryleVitamine E300 mg30 mg
Gluconate de zincZinc25 mg15 mg

Additives

E460, E341, E464, E170, E553b, E551, E470b, E1521, E422, E307

Other ingredients

gélatine

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

List recorded in 2022. Photograph the packaging to check whether it has changed. Photograph the packaging

Label warnings

Le produit n’est pas destiné à être consommé par des enfants (citicoline), par les femmes enceintes et le personnes sous antidépresseur (safran).

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.

Official warnings (Health Canada)

Health Canada publishes warnings on these ingredients:

They concern the ingredient, not this product or its dose. They do not replace medical advice.

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 2022. Photograph the packaging to check whether it has changed.

Enter to analyse, Shift+Enter for a new line