Frequently Asked Questions on food supplements

Food supplements are foods. They are intended to supplement the general diet. Food supplements may contain a broad spectrum of nutrients or other substances with a specific nutritional or physiological effect. They may be, for instance, vitamins, minerals, trace elements, amino acids, fatty acids, fibre, plants or herbal extracts which are added in concentrated form either individually or as a combination. Food supplements are sold in a dosed form, for instance as tablets, capsules, coated tablets, powders or liquids for intake in small, measured amounts. In contrast to other foods, food supplements may, among other things, come with a recommended intake along with other specific information for consumers, e.g. that they should be stored out of the reach of small children. The ingredients of food supplements may not, by definition, have any pharmacological effects. If a product of this kind has pharmacological effects, it falls under a different category than food supplements, e. g. under medicinal products which require official authorisation.

The German Food Supplements Regulation (NemV) specifies which vitamins and minerals and corresponding compound sources may be added to foods. Furthermore, other nutrients and substances with a specific nutritional or physiological effect may also be added to food supplements, but there are presently no provisions regulating which specific substances (e.g. amino acids, fatty acids, fibre, plants, herb extracts etc.) may be added. All the same, certain substances are equated with additives in Germany which means they are subject to prohibition with a reservation regarding the granting of permission. They may only be added to foods including food supplements when they have been explicitly approved through legal provisions for the respective purpose.

There are no binding maximum levels for the ingredients of food supplements either on the German national or the European level. However, the Food Supplements Directive (Directive 2002/46/EC) issued in 2002 already in principle makes provisions for the forseen setting of binding maximum levels for vitamins and essential minerals throughout Europe. Uniform maximum levels throughout Europe are desirable from the point of view of risk assessment. In 2018, the BfRshort forGerman Federal Institute for Risk Assessment revised its proposals for maximum levels for vitamins and essential minerals in food supplements, taking into account also intake via other sources, including intake via fortified foods (see Weißenborn, A., Bakhiya, N., Demuth, I. et al.short foret alii (lat. "and others") J Consum Prot Food Saf (2018) 13: 25. External Link:https://doi.org/10.1007/s00003-017-1140-y).

One main identifying characteristic of supplements is that they must be labelled as such, i.e. as a "food supplement". In addition to the details stipulated in the so-called Food Information Regulation (REG (EU) No. 1169/2011), they must - amongst others - bear information about the recommended daily intake as well as a warning that this amount must not be exceeded. Furthermore, the packaging must bear the information that food supplements should not be used as a substitute for a balanced, diverse diet and that they should be stored out of the reach of small children.

Claims to cure, alleviate or prevent disease are currently prohibited in Germany both in product advertising and on packaging. However, claims to reduce a risk of disease are possible, provided that they have been scientifically assessed by the European Food Safety Authority (EFSAshort forEuropean Food Safety Authority) in line with Regulation (EC) 1924/2006 (the so-called Health Claims Regulation) and have been explicitly authorised by the EU Commission.

As food supplements are foods, they are covered by the basic provisions of the German Food and Feed Code of Law (LFGB) as well as all other legislation of the European Union in the area of food law. Amongst other things, foods must be safe, consumers may not be misled by the information on the package and disease-related claims are prohibited. However, claims to reduce a risk of disease are possible after they have undergone official examination and been approved.

Food supplements are not subject to mandatory approval regulations. Pursuant to the German Food Supplements Regulation (NemV), food supplements must be registered with the Federal Office of Consumer Protection and Food Safety (BVLshort forGerman Federal Office of Consumer Protection and Food Safety). Responsibility for the safety of products and compliance with food law provisions lies with manufacturers and distributors. Monitoring of food supplements placed on the market and of manufacturing companies is the task of the food monitoring authorities of the German federal Laender.

Food supplements or other foods which do not comply with German food law provisions may only be placed on the market in Germany if they fulfil the precondition that they have been granted an exemption pursuant to § 68 of the Food and Feed Code Law (LFGB) or based on a general decree pursuant to § 54 LFGB.

An application for a general decree can be submitted to the Federal Office of Consumer Protection and Food Safety (BVLshort forGerman Federal Office of Consumer Protection and Food Safety) for food supplements which have been legally placed on the market in another Member State of the European Union. The application may only be rejected on compelling grounds of health protection or if the German authorities consider the supplement to be a medicinal product.

Domestic manufacturers or manufacturers from non-EU Member States also have the option of submitting an application for an exemption pursuant to § 68 of the Food and Feed Code Law (LFGB) to the BVLshort forGerman Federal Office of Consumer Protection and Food Safety. In this case, facts must justify the assumption that no risk to human health is to be expected. Here too, the precondition applies that the product in question is indeed to be classified as a food.

Medicinal products are intended to heal, alleviate, prevent or identify diseases, suffering, physical defects or health disorders, to replace active substances produced by the human or animal body, or to influence the condition, state or function of the body or the mental state. They are subject to, among others, the provisions of the Medicinal Products Act. Their ingredients are pharmacologically active. Medicinal products are subject to official authorisation by the Federal Institute for Drugs and Medical Devices (BfArM) or approval by the competent bodies of the European Union. During both types of authorisation procedure, their quality, efficacyClose dialogefficacyPositive Predictive ValueTo glossary and safety must be proven. Besides other important information on safe use, possible side effects that may occur during proper intake must be listed in a package leaflet.

Food supplements are foods and are subject to, among others, the provisions of the Food and Feed Code Law (LFGB). They are intended to supplement the diet and must be safe. Unlike medicinal products, they do not require official authorisation for which their safety must be proven. Food supplements may not be advertised by the use of any disease-related claims. However, claims to reduce the risk of disease are admissible provided that they have been scientifically assessed and confirmed by the European Food Safety Authority (EFSAshort forEuropean Food Safety Authority) in line with Regulation (EC) 1924/2006 (the so-called Health Claims Regulation) and have been explicitly authorised by the EU Commission. It is prohibited to mislead consumers.

The mere fact that a food supplement is on the market does not meanClose dialogmeanMeanTo glossary that the consumer can assume that this is a worthwhile or valuable food. Food supplements may also be on the market when their nutritional-physiological value is questionable.

It is possible that certain ingredients contained in food supplements are also used in medicinal products. Furthermore, food supplements are placed on the market in the same forms as medicinal products like tablets, capsules, powders or liquid preparations. This highlights the impression that food supplements and medicinal products appear to be, in some cases, very similar.

Under the federal system of the Federal Republic of Germany it is the federal Laender that check whether products have been legally placed on the market. They are responsible for organising official monitoring of medicinal products and foods. Within the framework of their competences, the monitoring authorities decide, based on an individual review, on the classification of a product as a medicinal product requiring official authorisation or as a food. Formal responsibility lies with the public authorities of the federal Land in which the product is on the market or in which the manufacturer, importer, supplier or distributor has its head office.

Because of differences in legal situations, products offered for sale on the Internet from outside Germany may be marketed in the countries of origin as food supplements but may be classified as medicinal products in Germany.

Irrespective of the distribution channel, the relevant German and European food law provisions naturally also apply to food supplements which are sold on the Internet. However, there have been reports of individual cases in which non-marketable food supplements were sold on the Internet. One example from the past concerned muscle-enhancing products. Investigations by the monitoring authorities in Germany had shown that some products sold on the internet as food supplements contained anabolic agents which had not been listed as ingredients.

When purchasing food supplements on the Internet, consumers should bear in mind that the use of the internet as a gateway to global markets offers not only opportunities but may also be linked to risks. In the case of the direct purchase of food supplements on the Internet from manufacturers/distributors outside Germany, it cannot simply be assumed that the products sold as food supplements comply with German and European food law provisions. Furthermore, consumers should thoroughly check whether the suppliers are reputable before buying food supplements.

The large number of food supplements on the market wrongly give the consumer the impression that sufficient nutrient intake is not possible solely from a diet comprising traditional foods. In principle a balanced, diverse diet supplies a healthy body with all the essential substances. In most cases, the intake of food supplements is therefore unnecessary.

However, there are exceptions to this general rule. An unbalanced or inadequate diet may lead to insufficient intake of essential nutrients. During pregnancy and breastfeeding there is an elevated need for specific nutrients. The intake of essential nutrients by elderly people may also be insufficient, for instance, as a consequence of chewing or swallowing disorders or a loss of appetite. The chronically ill may also have an elevated requirement for essential nutrients. In such cases, dietary supplementation may be necessary or advisable. Whenever a food supplement is used as an additional measure to treat or heal diseases like a chronic gastrointestinal tract disorder, however, this should always be done under medical supervision.

Data on nutrient intake indicate that the intake of a small number of vitamins and minerals like vitamin D, calcium, folic acid and iodine by some groups in the population does not meet the intake recommendations of the German Nutrition Society (DGE). However, this cannot generally be equated to insufficient supply or even a deficiency. In individual cases, however, dietary supplementation may be advisable. For instance, the intake of additional calcium by people who do not consume any dairy products may be considered. For several years now, table salt has been fortified with iodine in order to improve the iodine intake on a broad basis in the population in Germany.

Nevertheless, the best nutritional strategy is still a balanced, diverse diet with plenty of fruit and vegetables. Food supplements do not represent substitutes of equal value.

In the past, the BfRshort forGerman Federal Institute for Risk Assessment has adopted comprehensive stances on the possible risks from food supplements and has informed consumers about problems which could be linked to the consumption of these products. BfRshort forGerman Federal Institute for Risk Assessment opinions on food supplements or substances added to food supplements are used by management institutions at the federal level and by federal Land authorities to aid decision-making and as a basis for risk-reducing measures.

This text version is a translation of the original German text which is the only legally binding version.