Fer
Fer, licence 80023665: inactive licence in Health Canada data. The French and European references below do not constitute authorisation for sale in France or an assessment of safety or efficacy.
Licensed Natural Health Products Database (LNHPD), Health Canada: licensed products, ingredients, doses, uses and risks, retrieved 27 October 2026.
Contains information licensed under the Open Government Licence – Canada (Health Canada, LNHPD)
Licence du gouvernement ouvert – Canada 2.0 (OGL-Canada 2.0)
Natural health product licensed in Canada
- Other names
- Fer 45, Feramine, Iron, Iron 45, Mega Iron, Neobourne Pharma Mega Iron
- Licence holder
- BIOVANTEK
- NPN or DIN-HM
- 80023665
- Status
- Inactive licence
- Licence date
- 7 February 2011
- Revision date
- 17 May 2022
- Form
- Comprimé
- Route of administration
- Orale
- Application type
- Officinale
If this product were sold in France
- Dose déclarée au-delà d'une limite
Fer: up to 45 mg a day according to the dosing instructions published by Health Canada (1 unités posologiques par jour au plus, pour les adultes), above the maximum dose of 14 mg set in France for a food supplement (2006 Order, not revised since November 2006).
arrêté du 9 mai 2006, annexe III. French orders of 9 May 2006 and 14 November 2006 as published in the Official Journal (maximum daily doses), retrieved 21 October 2026.
- À vérifier
Fer: up to 45 mg a day according to the dosing instructions published by Health Canada, above the niveau de sécurité from EFSAEuropean Food Safety Authority. for adults (40 mg a day). Son dépassement ne permet pas, à lui seul, de caractériser un risque : l'EFSA n'a pas pu fixer de limite supérieure pour ce nutriment. Le repère de l'EFSA porte sur l'apport total d'une journée, alimentation et compléments.
niveau de sécurité. EFSA, Overview on Tolerable Upper Intake Levels (version 11, August 2025), retrieved 21 October 2026.
A daily quantity is calculated only for an explicit adult oral dosage, stated per day and in a solid unit matching the product form. Ambiguous units, liquids, powders and paediatric doses are not extrapolated. A quantity not calculated is not compared with dose limits. This analysis does not constitute authorisation for sale in France or an assessment of safety or efficacy.
Composition
| Medicinal ingredient and source | Per dosage unit, according to the source | Maximum per day, adult |
|---|---|---|
| Fer Source : Sulfate ferreux | 45.0 mg | 45,000 µg |
Non-medicinal ingredients
Macrogol 8 000, Alcool isopropylique, Jaune FD&C No. 5, Caramel, Dioxyde de titane, Cire de Carnauba, Talc, Cellulose microcristalline, Jaune FD&C n° 6, Eau purifiée, Croscarmellose de sodium, Oxyde de fer noir, Gomme-laque, Rouge FD & C no. 40, Stéarate de magnésium, Bleu FD&C n° 1, Dioxyde de silicium
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Adolescentes | minimum: 14.0 Année(s) | 1.0 Comprimé | 1.0 Jour(s) |
| Adultes | Not specified | 1.0 Comprimé | 1.0 Jour(s) |
Uses authorised in Canada
Aide à la formation de globules rouges et à leur bon fonctionnement. Aide à prévenir une carence en fer
A use authorised in Canada is not an authorised health claim in the European Union. See the health claims register.
Warnings in Canada
- Précautions et mises en garde
Garder hors de la portée des enfants. Ce contenant contient assez de médicament pouvant causer des torts sérieux à un enfant.
- Effets indésirables connus
Certaines personnes pourraient souffrir de constipation, de diarrhée ou de vomissement.
Source
Official Health Canada record, licence 80023665
The formula sold in Europe under the same name may differ. This information does not replace advice from a doctor or pharmacist.
List in the official revision dated (register: Licensed Natural Health Products Database (LNHPD), Health Canada: licensed products, ingredients, doses, uses and risks).
List recorded in 2022. Photograph the packaging to check whether it has changed.
Has the product changed? Photograph the packaging.