ZENIDOSE
Food supplement declared in France, declaration No 2016-9-6
ZENIDOSE is a food supplement declared in France. Status: retiré du marché le 29 June 2020. 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
- SAS S.I.D. NUTRITION
- Status
- Retiré du marché le 29 June 2020
- Form
- Flacon
- Daily dose
- 20 ml par jour
- Directions for use
- Diluer 20 ml de liquide dans un grand verre d'eau 1 fois par jour.
- Not recommended for (according to the manufacturer)
- Femmes allaitantes, Femmes enceintes
- Objectives stated by the manufacturer (these are not authorised claims)
- Sommeil
Declaration 196160, procedure Article 15. Compl'Alim, food supplement declarations (France), retrieved 23 October 2026.
Regulatory points
- Information
Retiré du marché le 29 June 2020, according to Compl'Alim.
Source: Compl'Alim, food supplement declarations (France).
Declared composition
Plants
| Plant | Part | Preparation | Per day |
|---|---|---|---|
| Crataegus monogyna Jacq. | Sommités fleuries | Extrait sec aqueux | 40 mg |
| Papaver rhoeas L. | Fleur | Extrait sec aqueux | 28 mg |
| Sedum roseum (L.) Scop. | Racine | Extrait sec hydroalcoolique | 20 mg |
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 |
|---|---|---|---|
| Chlorure de magnésium | Magnésium | 250 mg | 300 mg |
Additives
E422, E338, E202, E211, E955
Other ingredients
eau
The evidence date of this ingredient list is unknown.
Has the product changed? Photograph the packaging.
Label warnings
Déconseillé aux femmes enceintes et allaitantes.
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.