Arthromarine
Food supplement declared in France, declaration No 2017-6-2
Arthromarine (Pharmatech) is a food supplement declared in France. Status: retiré du marché le 8 February 2025. 1 rule of use applies to its ingredients (limits and warnings).
- Brand
- Pharmatech
- Food business operator placing the product on the market
- MGD (FLOWER CAPS)
- Status
- Retiré du marché le 8 February 2025
- Form
- Gélule
- Daily dose
- 5 gélules
- Directions for use
- 2 gélules le matin et 3 gélules le soir
- Intended populations
- Personnes de plus de 60 ans, Homme, Femme
- Not recommended for (according to the manufacturer)
- Sous anticoagulants
- Objectives stated by the manufacturer (these are not authorised claims)
- Articulations
Declaration 150479, procedure Article 16. Compl'Alim, food supplement declarations (France), retrieved 23 October 2026.
Regulatory points
- Conditions légales
Urtica dioica L.: L'étiquetage des compléments alimentaires contenant les parties souterraines de cette plante doit comporter une mention recommandant de prendre conseil auprès d'un professionnel de santé ("Demander l'avis de votre médecin et /ou pharmacien").
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 8 February 2025, according to Compl'Alim.
Source: Compl'Alim, food supplement declarations (France).
Declared composition
Plants
| Plant | Part | Preparation | Per day |
|---|---|---|---|
| Urtica dioica L. | Feuille | Extrait sec aqueux | 300 mg |
| Curcuma longa L. | Rhizome | Extrait sec alcoolique | 150 mg |
Other active ingredients
| Name | Per day |
|---|---|
| Chlorhydrate de glucosamine | not declared |
| Sulfate de chondroïtine | 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 |
| Gluconate de manganèse | Manganèse | 8 mg (niveau de sécurité) | 3.5 mg |
| Acide L-ascorbique | Vitamine C | pas de limite (données insuffisantes) | 180 mg |
Additives
E1204, E553b, E470b
The evidence date of this ingredient list is unknown.
Has the product 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.
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.
- ARTHROMarine PHARMATECH, declared in 2021 : different composition: 0 ingredient(s) added, 1 missing
- ARTHROMarine MGD (FLOWER CAPS), declared in 2019 : different composition: 0 ingredient(s) added, 1 missing
- ARTHROMarine MGD, declared in 2017 : different composition: 3 ingredient(s) added, 1 missing
- ARTHROMarine MGD, declared in 2017, withdrawn from the market : same declared composition
Brand : Pharmatech