SANAFLORE
Food supplement declared in France, declaration No 2019-6-399
SANAFLORE is a food supplement declared in France. Status: retiré du marché le 31 October 2025. 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
- Agir Luxembourg SA
- Status
- Retiré du marché le 31 October 2025
- Form
- Gélule
- Daily dose
- 1 gélule
- Directions for use
- Prendre 1 gélule par jour
- Not recommended for (according to the manufacturer)
- Femmes allaitantes, Femmes enceintes
Declaration 295973, procedure Article 15. Compl'Alim, food supplement declarations (France), retrieved 23 October 2026.
Regulatory points
- Information
Retiré du marché le 31 October 2025, according to Compl'Alim.
Source: Compl'Alim, food supplement declarations (France).
Declared composition
Other active ingredients
| Name | Per day |
|---|---|
| Dolomite | 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 |
|---|---|---|---|
| Nicotinamide | Nicotinamide (vitamine B3) | 900 mg | 54 mg |
| Chlorhydrate de thiamine | Vitamine B1 (thiamine) | pas de limite (données insuffisantes) | dose annulée par le Conseil d'État en 2011 |
| Chlorhydrate de pyridoxine | Vitamine B6 | 12 mg | 2 mg |
| Citrate de zinc | Zinc | 25 mg | 15 mg |
Additives
E460, E1204
Other ingredients
Extrait de riz
The evidence date of this ingredient list is unknown.
Has the product changed? Photograph the packaging.
Label warnings
Il est recommandé aux femmes enceintes ou allaitantes de 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.