Iron in food supplements
3,535 supplements declared in France contain a form of this nutrient
Iron: in France, a food supplement may not provide more than 14 mg a day (Order of 9 May 2006, not revised since November 2006, Annex III); for adults, EFSA's safe level (no upper limit established) is 40 mg a day. The doses of the 2006 Order have not been revised since the amending Order of 14 November 2006, and some were annulled by the Conseil d'État in 2011; the DGCCRF accepted higher levels for some nutrients through guidelines published until January 2019, and an update of the Order is being prepared (ministerial answer published in the Official Journal on 11 February 2025).
Order of 9 May 2006, Annex III. French orders of 9 May 2006 and 14 November 2006 as published in the Official Journal (maximum daily doses), retrieved 21 October 2026.
EFSA, Overview on Tolerable Upper Intake Levels (version 11, August 2025), retrieved 21 October 2026.
Written Question No 2686, ministry answer published in the Official Journal on 11 February 2025.
What we know about this ingredient
Associated research
ClinicalTrials.gov · A trial is not proof: it tests a hypothesis.
- NCT06670963 : Use of Epoetin Alfa and Iron Derisomaltose in Treatment of Anemia in Patients With Sepsis or Septic Shock: a Randomized Controlled Trial
RECRUITING · PHASE4 · Anemia, Sepsis, Septic Shock · 2024-12-27 · Iron
- NCT06637137 : Patient Blood Management in Patients Scheduled for Cardiac Surgery
RECRUITING · Anemia, Anemia, Iron-Deficiency, Iron Deficiency Anemia Treatment, Iron Deficiency Anemia (IDA), Cardiac Surgical Patients, Blood Loss, Surgical · 2026-09-10 · Iron
- NCT07814378 : Impact of Iron Supplementation During Pregnancy
NOT_YET_RECRUITING · Anemia, Iron Deficiency Anaemia in Childbirth, Pregnancy · 2026-09-11 · Iron
2026-11-01
In plain words
À quoi il sert, selon les fabricants
Objectifs les plus souvent annoncés pour les compléments qui en contiennent (fer) : immunité (753 produits), cheveux et ongles (368 produits), sport (295 produits), grossesse et allaitement (226 produits), système nerveux (208 produits).
Ce sont les objectifs déclarés par les fabricants à l'administration, pas des effets démontrés. Sur l'emballage, seules les allégations de santé autorisées par l'Union peuvent être écrites.
Compl'Alim, food supplement declarations (France), retrieved 23 October 2026.
Jusqu'où c'est sûr
Pour un adulte, les données ne suffisent pas à l'EFSAEuropean Food Safety Authority. pour fixer une limite supérieure. Elle indique un niveau de sécurité de 40 mg/j : en dessous, on peut être raisonnablement sûr de l'absence d'effet indésirable ; au-dessus, l'EFSA ne peut pas évaluer le risque faute de données.
Précision de l'EFSA : Pas de limite supérieure : niveaux de sécurité (safe levels), qui ne caractérisent pas un risque en cas de dépassement ; avant 1 an, apport supplémentaire seulement (compléments et aliments enrichis).
EFSA, Overview on Tolerable Upper Intake Levels (version 11, August 2025), retrieved 21 October 2026.
La règle en France
En France, la dose journalière recommandée d'un complément ne doit pas apporter plus de 14 mg (arrêté du 9 mai 2006, non révisé depuis novembre 2006). Compl'Alim ne publie pas la dose des produits déclarés : comparez celle de l'étiquette à ce plafond et à la limite de sécurité de l'EFSA.
French orders of 9 May 2006 and 14 November 2006 as published in the Official Journal (maximum daily doses), retrieved 21 October 2026.
EFSA safety references
Le repère de l'EFSA porte sur l'apport total d'une journée, alimentation et compléments.
| Population | Type | Value |
|---|---|---|
| 4-6 months | Safe level | 5 mg/j |
| 7-11 months | Safe level | 5 mg/j |
| 1-3 years | Safe level | 10 mg/j |
| 4-6 years | Safe level | 15 mg/j |
| 7-10 years | Safe level | 20 mg/j |
| 11-14 years | Safe level | 30 mg/j |
| 15-17 years | Safe level | 35 mg/j |
| adults | Safe level | 40 mg/j |
| pregnancy | Safe level | 40 mg/j |
| breastfeeding | Safe level | 40 mg/j |
No upper limit: safe levels, which do not characterise a risk when exceeded; below 1 year, additional intake only (supplements and fortified foods)
EFSA NDA Panel, 2024b. EFSA, Overview on Tolerable Upper Intake Levels (version 11, August 2025), retrieved 21 October 2026.
Maximum dose in France
Maximum daily dose per supplement in France: 14 mg, according to the Order of 9 May 2006.
The doses of the 2006 Order have not been revised since the amending Order of 14 November 2006, and some were annulled by the Conseil d'État in 2011; the DGCCRF accepted higher levels for some nutrients through guidelines published until January 2019, and an update of the Order is being prepared (ministerial answer published in the Official Journal on 11 February 2025).
Order of 9 May 2006, Annex III. French orders of 9 May 2006 and 14 November 2006 as published in the Official Journal (maximum daily doses), retrieved 21 October 2026.
Authorised health claims
- « Iron contributes to normal cognitive development of children »
Conditions: The claim can be used only for food which is at least a source of iron as referred to in the claim SOURCE OF [NAME OF VITAMIN/S] AND/OR [NAME OF MINERAL/S] as listed in the Annex to Regulation (EC) No 1924/2006 - « Iron contributes to normal cognitive function »
Conditions: The claim may be used only for food which is at least a source of iron as referred to in the claim SOURCE OF [NAME OF VITAMIN/S] AND/OR [NAME OF MINERAL/S] as listed in the Annex to Regulation (EC) No 1924/2006. - « Iron contributes to normal energy-yielding metabolism »
Conditions: The claim may be used only for food which is at least a source of iron as referred to in the claim SOURCE OF [NAME OF VITAMIN/S] AND/OR [NAME OF MINERAL/S] as listed in the Annex to Regulation (EC) No 1924/2006. - « Iron contributes to normal formation of red blood cells and haemoglobin »
Conditions: The claim may be used only for food which is at least a source of iron as referred to in the claim SOURCE OF [NAME OF VITAMIN/S] AND/OR [NAME OF MINERAL/S] as listed in the Annex to Regulation (EC) No 1924/2006. - « Iron contributes to normal oxygen transport in the body »
Conditions: The claim may be used only for food which is at least a source of iron as referred to in the claim SOURCE OF [NAME OF VITAMIN/S] AND/OR [NAME OF MINERAL/S] as listed in the Annex to Regulation (EC) No 1924/2006. - « Iron contributes to the normal function of the immune system »
Conditions: The claim may be used only for food which is at least a source of iron as referred to in the claim SOURCE OF [NAME OF VITAMIN/S] AND/OR [NAME OF MINERAL/S] as listed in the Annex to Regulation (EC) No 1924/2006. - « Iron contributes to the reduction of tiredness and fatigue »
Conditions: The claim may be used only for food which is at least a source of iron as referred to in the claim SOURCE OF [NAME OF VITAMIN/S] AND/OR [NAME OF MINERAL/S] as listed in the Annex to Regulation (EC) No 1924/2006. - « Iron has a role in the process of cell division »
Conditions: The claim may be used only for food which is at least a source of iron as referred to in the claim SOURCE OF [NAME OF VITAMIN/S] AND/OR [NAME OF MINERAL/S] as listed in the Annex to Regulation (EC) No 1924/2006.
3 refused or revoked claims: they cannot appear on packaging
- « Excessive hair loss in non-menopausal women »
Reason: Non-compliance with the Regulation because on the basis of the scientific evidence assessed, this claimed effect for this food has not been substantiated. - « Iron affects activity of heart, liver and muscles. »
Reason: Non-compliance with the Regulation because on the basis of the scientific evidence assessed, this claimed effect for this food is not sufficiently defined to be able to be assessed and the claim could not therefore be substantiated. - « Iron is needed to allow the body metabolise drugs and other substances. Iron contributes to the body’s ability to metabolise drugs and other substances. Iron is needed for the metabolism of drugs. »
Reason: Non-compliance with the Regulation because on the basis of the scientific evidence assessed, this claimed effect for this food is not sufficiently defined to be able to be assessed and the claim could not therefore be substantiated.
Official English text, as entered in the Union register. A claim may only be used under its conditions.
8 authorised claims, 3 refused or revoked. EU Register of nutrition and health claims, retrieved 21 October 2026.
Forms declared in supplements
Union list: vitamin and mineral forms that may be used in a food supplement (Directive 2002/46/EC, Annex II).
Directive 2002/46/EC on food supplements, latest consolidated version (Annex II: forms of vitamins and minerals), retrieved 23 October 2026.
- Bisglycinate ferreux 1,050 products on the Union list
- Fumarate ferreux 785 products on the Union list
- Gluconate ferreux 712 products on the Union list
- Pyrophosphate ferrique 359 products on the Union list
- Sulfate ferreux 311 products on the Union list
- Citrate ferreux 93 products on the Union list
- Lactate ferreux 75 products on the Union list
- Fer élémentaire 66 products on the Union list
- L-pidolate ferreux 56 products on the Union list
- Sel de sodium de l'édétate de fer (III) 38 products on the Union list
- Saccharate ferrique 20 products on the Union list
- Citrate d'ammonium ferrique 8 products on the Union list
- Diphosphate de sodium ferrique 7 products on the Union list
- Phosphate ferreux 5 products on the Union list
- Carbonate ferreux 3 products on the Union list
- Tartrate-adipate d’hydroxyde de fer 2 products on the Union list
- Taurate de fer (II) 1 product on the Union list
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