Germany: NMN Classified as a Medicinal Product

Summary

The Federal Office of Consumer Protection has classified NMN (Nicotinamide Mononucleotide) as a medicinal product. Sale as a dietary supplement is prohibited.

Background

This article addresses recent developments in dietary supplement regulations. The information provided is based on official publications from EFSA, BfR, UK FSA, and other European authorities.

Key Points

• Point 1: Regulatory changes have a direct impact on your products
• Point 2: Compliance checks should be conducted regularly
• Point 3: Multi-country launches require country-specific adjustments
• Point 4: Health claims must strictly adhere to EFSA guidelines
• Point 5: Labeling requirements vary between EU member states

Practical Recommendations

For Manufacturers

1. Immediate Review: Assess your existing formulations
2. Documentation: Ensure complete compliance documentation
3. Multi-Market: Take country-specific requirements into account
4. Timeline: Plan reformulations in a timely manner

For Distributors

1. Supplier Check: Request up-to-date compliance documents
2. Product Review: Use automated tools like Supplement-Check.eu
3. Inventory: Check existing stock for compliance
4. Marketing: Adjust claims and descriptions

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Conclusion

The regulatory landscape for dietary supplements in Europe is continuously evolving. Regular compliance checks are essential to avoid sales bans, warnings, and hefty fines.

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Published on: 2025-06-25
Category: legislation
Reading time: 8 minutes

Disclaimer: This article is for informational purposes only and does not constitute legal advice. For legally binding information, please consult a specialist lawyer in food law.