lutéine myrtille
Food supplement declared in France, declaration No 2019-11-919, decision dated 23 November 2019
lutéine myrtille 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.
- Brand
- not provided
- Food business operator placing the product on the market
- LABORATOIRE PARAPHAR
- 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
- 1920 mg
- Directions for use
- 1 à 2 à 3 gélules par jour
- Objectives stated by the manufacturer (these are not authorised claims)
- Œil / Vision
Declaration 298915, 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
| Plant | Part | Preparation | Per day |
|---|---|---|---|
| Vaccinium myrtillus L. | Baie | Poudre (de plantes séchées ou broyées) | 1,650 mg |
Other active ingredients
| Name | Per day |
|---|---|
| Lutéine | not declared |
| Zéaxanthine | not declared |
Other ingredients
gélatine
List from the declaration, administrative decision dated (Compl'Alim, food supplement declarations (France)).
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:
- Vaccinium myrtillus L.
Read the warning, when it applies and the studies cited
BILBERRY - VACCINIUM MYRTILLUS - Buccal
Route of administration: Buccal (Blumenthal et al. 2000)
Cautions and warnings
Ask a health care practitioner/health care provider/health care professional/doctor/physician if symptoms persist or worsen.
Health Canada monograph dated 30 January 2026
BILBERRY - VACCINIUM MYRTILLUS - Oral
Route of administration: Oral (Blumenthal et al. 2000)
Cautions and warnings
Condition of application: Relief of diarrhea.
Ask a health care practitioner/health care provider/health care professional/doctor/physician if symptoms persist or worsen.
Condition of application: Slowing the progression of disorders of the eye and to relieve symptoms related to non-complicated CVI.
Ask a health care practitioner/health care provider/health care professional/doctor/physician if symptoms worsen.
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.
- LUTEINE MYRTILLE JUVAMINE, declared in 2026 : different composition: 5 ingredient(s) added, 2 missing
- Lutéine Myrtille VITAVEA - Laboratoires Yves Ponroy, declared in 2025 : different composition: 7 ingredient(s) added, 3 missing
- Lutéine Myrtille Laboratoires Juvamine, declared in 2022 : different composition: 5 ingredient(s) added, 2 missing
- Lutéine Myrtille Laboratoires VITARMONYL, declared in 2020, withdrawal announced : different composition: 5 ingredient(s) added, 3 missing
- lutéine myrtille LA CROIX BLANCHE DIJON FRANCE, declared in 2018 : same declared composition
- Lutéine Myrtille VITAVEA - Laboratoires Yves Ponroy, declared in 2024, earlier declaration, replaced by the 2025 declaration : different composition: 7 ingredient(s) added, 3 missing
- Lutéine Myrtille laboratoires Yves Ponroy, declared in 2021, earlier declaration, replaced by the 2025 declaration : different composition: 5 ingredient(s) added, 3 missing
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