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K2
Beyuna K2 contains vitamin K2 in the patented form K2VITAL® DELTA. In K2VITAL® DELTA, the highly absorbable vitamin K2-MK7 is double encapsulated for complete stability. Additionally, Beyuna K2 consists of alfalfa herb and rice flour.
Vitamin K contributes to normal blood clotting and it contributes to the maintenance of strong bones. Vitamin K contributes to the absorption of minerals/calcium into the bones/bone tissue.
Beyuna K2 features a plant-based pullulan capsule, making it suitable for vegans. Beyuna K2 is Clean Label, it does not contain synthetic fillers, additives, or colorants, and it is GMO-free.
Contents: 30 plant-based capsules
BEYUNA K2
The recommended dosage for adults is 1 capsule per day.
1 capsule contains:
| Ingredients | *R.I. | Content | |
|---|---|---|---|
| Alfalfa herb | 150 mg | ||
| Vitamin K2 (Vital Delta 1%) | 267% | 200 µg | |
| Rice flour | 10 mg |
*RI = Reference Intakes for adults
Capsule: vegetable
BEYUNA K2
| Vitamin K |
|---|
| Vitamin K contributes to proper blood clotting |
| Vitamin K aids in normal blood clotting |
| Vitamin K supports blood clotting |
| Vitamin K, in the absorption of minerals/calcium into the bones/bone tissue |
| Vitamin K contributes to the maintenance of strong bones |
| Vitamin K is important for bone composition |
| Vitamin K supports bone health |
| Vitamin K for the preservation of strong bones |
| Vitamin K, beneficial for the skeleton |
| Vitamin K plays a role in bone formation |
BEYUNA K2
| USE |
|---|
| Take one capsule per day with a glass of water with a meal. |
| Do not exceed the recommended daily dosage. |
| A dietary supplement is not a substitute for a varied diet. |
| A healthy lifestyle and a varied, balanced diet is vital to maintain good health. |
| STORAGE RECOMMENDATIONS |
| Dark, closed, cool and out of the reach of young children. |
BEYUNA K2
According to EC Directives 2000/13, 2003/89, 2005/26, 2005/63, 2006/142, 2007/68 and updates.
| Allergens | Yes/No |
|---|---|
| Cereals containing gluten and products thereof | No |
| Crustaceans and products thereof | No |
| Eggs and products thereof | No |
| Fish and products thereof | No |
| Peanuts and products thereof | No |
| Soy/ Soyderivatives | No |
| Milk and products thereof, including lactose | No |
| Nuts and products thereof | No |
| Celery and products thereof | No |
| Mustard and products thereof | No |
| Sesame seeds and products thereof | No |
| Sulphur dioxide and sulphites at concentrations of more than 10 mg/l, expressed as SO | No |
| Lupin and products thereof | No |
| Molluscs and products thereof | No |
GMO-Free
European legislation was adopted in 2012 relating to nutrition and health claims made on foods (the Commission Regulation). The Commission Regulation is a European Regulation (432/2012) which sets out what information may be provided regarding the effect of vitamins, minerals and other nutrients on products (on packaging, labels, websites, advertisements, in brochures, books and on social media).
Only approved health claims may be made. These claims provide information about the effect a particular ingredient has on health. Approved health claims are recommended by the European Food Safety Authority (EFSA). For many years, it was possible for companies to submit health claims, but unfortunately very few of them were approved. Because many of the claims submitted were rejected, some nutrients have no approved claims which relate to them.
Food supplements are not a medication and may only promote health. This means medical claims can never be made in relation to supplements.
We all enjoy free speech, and it is possible to make claims about the effect of certain nutrients in articles and brochures and on websites, but in this case there should be no advertising of a specific product or any reference made to it.
The Inspection Board for the Promotion of Health Products
Public advertising of self-care medicines, medical (self-care) aids or health products is in the interest of public health, though it does require clear regulations. Industry, the media and advertisers recognise their social responsibilities, and have created rules with which public advertising must comply.
These rules are drawn up by the Dutch Foundation for Monitoring Medicinal Product Advertising (KOAG) and the Dutch Foundation for the Promotion of Health Products (KAG). On behalf of the KOAG and KAG, the Inspection Board monitors the public advertising of medicines, medical (self-care) aids and health products.
Companies can have their claims verified by KOAG KAG. If a claim is verified and permitted, the company is given an approval number. This can be found on claims made in, e.g., brochures.
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