HemeBoost
HemeBoost, licence 80088471: active 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
- Licence holder
- Pharmaris Canada Inc.
- NPN or DIN-HM
- 80088471
- Status
- Active licence
- Licence date
- 26 September 2018
- Revision date
- 12 April 2019
- Form
- Comprimé
- Route of administration
- Orale
- Application type
- Non traditionnelle
If this product were sold in France
- Dose déclarée au-delà d'une limite
Fer: up to 34.8 mg a day according to the dosing instructions published by Health Canada (3 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.
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 : Heme iron polypeptide | 11.6 mg | 34,800 µg |
Non-medicinal ingredients
Poly(alcool vinylique), Croscarmellose de sodium, Dicalcium phosphate, Hydroxypropylméthylcellulose, Dioxyde de silicium, Carbonate de calcium, Hydroxypropylcellulose, Dioxyde de titane, Poly(éthylène glycol), Cellulose microcristalline, Stéarate de magnésium, Talc, Amidon prégélatinisé, Laque d'aluminiium FD&C rouge n° 40
Recommended doses in Canada
| Population | Age | Quantity per serving | Frequency |
|---|---|---|---|
| Adultes | minimum: 19.0 Année(s) | 1.0 Comprimé | minimum: 2.0 Tous les jours ; maximum: 3.0 Tous les jours |
Uses authorised in Canada
Helps to prevent Iron defeciency and its anemia.
A use authorised in Canada is not an authorised health claim in the European Union. See the health claims register.
Warnings in Canada
- Effets indésirables connus
May experience constipation, diarrhoea, and/or vomiting. Iron may cause your stools to turn black, an effect that is not harmful. A very serious allergic reaction to this product is rare. Persons with known allergies to meat products should not consume this product. Hypersensitivity has been known to occur; in which case, discontinue use.
- Précautions et mises en garde
Consult a medical advisor before consuming, if you have/are: anemia, hereditary hemochromatosis, other conditions of iron overloading (including blood transfusions) and/or gastro-intestinal concerns; or using methyldopa or other iron containing products. KEEP OUT OF REACH OF CHILDREN. This product contains enough drug to seriously harm a child.
- Contre-indications
Iron supplements can decrease the absorption of drugs such as tetracycline antibiotics, penicillamine, cefdinir, chloramphenicol, levothyroxine, levodopa and quinolone antibiotics. Therefore, doses of these medications should be spaced as far as possible. This product may interfere with certain laboratory tests (including testing for blood in stool) possibly causing false test results. Make sure laboratory personnel and all doctors know you are taking this product.
Source
Official Health Canada record, licence 80088471
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 2019. Photograph the packaging to check whether it has changed.
Has the product changed? Photograph the packaging.