PHYTO-OPTIC 1
Food supplement declared in France, declaration No 2019-9-175
PHYTO-OPTIC 1 (INTERPHYT) is a food supplement declared in France. Status: retiré du marché le 19 June 2025. 1 rule of use applies to its ingredients (limits and warnings).
- Brand
- INTERPHYT
- Food business operator placing the product on the market
- SAS INTERPHYT
- Status
- Retiré du marché le 19 June 2025
- Form
- Gélule
- Daily dose
- 1 GELULE
- Directions for use
- A PRENDRE AVEC UN GRAND VERRE D'EAU
- Intended populations
- Personnes de plus de 60 ans, Homme, Femme
- Not recommended for (according to the manufacturer)
- Femmes allaitantes, Enfants (moins de 12 ans), Enfants en bas âge (1 à 3 ans), Femmes enceintes, Sous anticoagulants, Sous antidépresseurs
- Objectives stated by the manufacturer (these are not authorised claims)
- Œil / Vision
Declaration 165435, procedure Article 15. Compl'Alim, food supplement declarations (France), retrieved 23 October 2026.
Regulatory points
- Conditions légales
Ginkgo biloba L.: L'étiquetage des compléments alimentaires qui contiennent la feuille de la plante Ginkgo biloba L. doit comporter un avertissement avec la teneur suivante: "Consultez votre médecin en cas de prise simultanée d'anticoagulants."
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 19 June 2025, according to Compl'Alim.
Source: Compl'Alim, food supplement declarations (France).
Declared composition
Plants
| Plant | Part | Preparation | Per day |
|---|---|---|---|
| Malpighia glabra L. | Fruit | Autre extrait sec | 210 mg |
| Vaccinium myrtillus L. | Fruit | Poudre (de plantes séchées ou broyées) | 17 mg |
| Ginkgo biloba L. | Feuille | Poudre (de plantes séchées ou broyées) | 10 mg |
Other active ingredients
| Name | Per day |
|---|---|
| Lutéine | not declared |
| Astaxanthine | not declared |
| Resvératrol | 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 |
| D-alpha-tocophérol | Vitamine E | 300 mg | 30 mg |
| Gluconate de zinc | Zinc | 25 mg | 15 mg |
Additives
E470b
The evidence date of this ingredient list is unknown.
Has the product changed? Photograph the packaging.
Label warnings
Consultez votre médecin en cas de prise simultanée d'anticoagulants. Déconseillé aux personnes sous traitement antidépresseur ainsi qu'aux femmes enceintes ou allaitant.
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.
- PHYTO-OPTIC 1 INTERPHYT, declared in 2017, withdrawn from the market : same declared composition
Brand : INTERPHYT