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Food supplements

Food supplements are used for supplementing the daily diet. Examples of different types of food supplement products are multivitamin tablets and fish oil capsules. At this page you will find information concerning the legislation on food supplements.

​​​​The purpose of food supplements is to supplement the daily diet. They are a concentrated source of nutrients and usually contain vitamins, minerals, plant ingredients, or concentrated substances such as omega-3 fatty acids or amino acids.

​​​Marketing of food supplem​​​e​nts in De​​​nmark
In order to sell food supplements in Denmark, any company is required to register the products no later than the first day of marketing. All food business operators have to be registered or approved by the Danish Veterinary and Food Administration (DVFA). This also applies for importers of food from other EU member states or third countries and producers/importers of food contact materials (FCM).
 
More information regarding starting a new food business in Denmark is found here and you can download an English version of the registration form here.
 
Changes in the composition of an existing food supplement requires a new registration as if it was a new product. An exception to this rule concerns changes in food additives which  do not require a new registration.  
 
Companies need to unregister any food supplements they no longer wish to sell in Denmark. Unregistered food supplements are not allowed to be marketed from neither the wholesale company, websites, nor retail stores.
 

Fee for product safety checks

Companies that have registered one or more food supplements in Denmark and that have an annual turnover exceeding 50,000 DKK are required to pay an annual fee of 9,573 DKK for extra inspection and an annual fee of 766 DKK per registered food supplement (2020). These fees are used to cover the expenses in relation to product safety checks. The payments are charged for companies and products registered as of February 1 that same year.
Regulations on the composition of fo​od supplements
 
In addition, food supplements sold in Denmark are governed by the Commission Regulation (EC) No 1170/2009, Commission Regulation (EU) No 1161/2011, Commission Regulation (EU) No 119/2014, Commission Regulation (EU) No 2015/414 as well as the Danish regulation on food supplements "Kosttilskudsbekendtgørelsen".
 
A written guidance on the regulation of food supplements is only available in Danish.
The guidance contains the DVFA's recommendation for maximum levels of different vitamins and minerals in the food supplements. If a company wishes to exceed these levels, they must be responsible for documenting the safety of the food supplement. The DVFA typically considers a level above the Tolerable Upper Intake Level  (UL) determined by European Food Safety Authority (EFSA) as a potential health risk.   
 
National regulation govern the addition of other substances than vitamins and minerals- You can find more information in our guide on fortified food. This guide also explains the legislative difference between plant ingredients and other substances in Denmark.   


Additional food regulations

In addition to the above-mentioned rules and regulations, there are specific rules for some aspects:
Labelli​ng of food supplements

Food supplements are required to follow the general food labelling rules specified in Regulation (EU) No 1169/2011 and the Danish regulation on labelling "Mærkningsbekendtgørelsen". The Danish legislation requires that the labelling on a food product in Denmark has to be readable and written in Danish or a similar language. It is required that the labelling contains a list of ingredients, the name of the food as well as the company, which is responsible for the production. 

In addition to the above-mentioned general requirements, food supplements should also be labelled with:

  • Information stating that the product is a food supplement.
  • Vitamins, minerals or other ingredients that the product contains.
  • The amount of vitamins, minerals or other ingredients in the product.
  • The Danish and Latin name of any herbal ingredients.
  • The recommended daily dose.
  • A warning not to consume more than the recommended daily dose.
  • Information stating that food supplements should not replace a healthy and varied diet.
  • A warning to keep the product out of reach of children.
  • The amount of nutrients or substances with a nutritional and/or physiological effect.
  • The amount of nutrients or other substances expressed as a percentage of the recommended daily dose.
  • The amount of vitamins and minerals expressed as a percentage of the reference values set out in Annex XIII, Part A, Point 1 in Regulation (EU) No 1169/2011 of the European Parliament and the Council of 25 October 2011 on the provision of food information to consumers.

​Nutrition and health claims on food suppl​ements

The use of nutrition and health claims on food supplements is voluntary. In order to use the different claims, they must comply with the rules specified in Regulation (EC) No 1924/2006 of the European Parliament and the Council. Products that are claimed to prevent or cure diseases are considered medicinal products and these are regulated by the Danish Medicines Agency.   

Own-check programme

An own-check programme is a plan that shows how a company, which sells and/or produces food products regularly ensures that the business and production complies with the rules. The own-check programme deals with foodstuffs as well as cleaning, machinery, and premises. The program must be readable to ensure that all employees can understand it and have no doubt as to what needs to be done. There is more information on about own-check programmes in our guide

Last Modified 24. February 2020