CLINALGIC FORTE
Food supplement declared in France, declaration No 2016-12-929, decision dated 27 December 2016
CLINALGIC FORTE 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). 1 point in its composition requires a check (prohibited substance, dose or novel food). 1 rule of use applies to its ingredients (limits and warnings).
- Brand
- not provided
- Food business operator placing the product on the market
- EXDER
- 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 par jour
- Directions for use
- Avaler avec un verre d'eau
- Intended populations
- Personnes de plus de 60 ans, Homme, Femme
- Not recommended for (according to the manufacturer)
- Femmes allaitantes, Allergie aux dérivés salicylés, Enfants (moins de 12 ans), Enfants en bas âge (1 à 3 ans), Femmes enceintes
- Objectives stated by the manufacturer (these are not authorised claims)
- Articulations
Declaration 278042, procedure Article 15. Compl'Alim, food supplement declarations (France), retrieved 23 October 2026.
Regulatory points
- À vérifier
The composition lists additive E171 (titanium dioxide), removed from the list of additives allowed in food, supplements included: since 7 August 2022, a supplement containing it can no longer be placed on the market in the Union. The declaration predates this removal: if the product is still sold, its formula must have changed; check the label.
Source: Regulation (EU) 2022/63: titanium dioxide (E171) removed from the food additives allowed in the EU, règlement (UE) 2022/63.
- Conditions légales
Salix alba L.: L'étiquetage doit comporter un avertissement déconseillant l'emploi aux personnes souffrant d'allergie aux dérivés salicylés.
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.
Declared composition
Plants
| Plant | Part | Preparation | Per day |
|---|---|---|---|
| Boswellia serrata Roxb. ex Colebr. | Gomme résine | Extrait sec aqueux | 614 mg |
| Salix alba L. | Ecorce | Extrait sec hydroalcoolique | 150 mg |
| Harpagophytum procumbens | Racine | Extrait sec hydroalcoolique | 100 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 |
|---|---|---|---|
| Gluconate de cuivre | Cuivre | 5,000 µg | 2,000 µg |
| Gluconate de manganèse | Manganèse | 8 mg (niveau de sécurité) | 3.5 mg |
| Acide orthosilicique stabilisé par de la choline | Silicium | pas de limite (données insuffisantes) | aucune dose fixée |
| Acide L-ascorbique | Vitamine C | pas de limite (données insuffisantes) | 180 mg |
Additives
E460, E341, E470b, E551, E464, E570, E171, E172, E132
List from the declaration, administrative decision dated (Compl'Alim, food supplement declarations (France)).
List recorded in 2016. Photograph the packaging to check whether it has changed. Photograph the packaging
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.