Eurofins US Food Announcements & News

Consumers rely on sunscreen to provide dependable protection against UV radiation, one of the leading causes of skin damage, premature aging, and skin cancer. Because of this, sunscreen manufacturers face a unique responsibility: to ensure every product consistently delivers the level of protection stated on the label. Read more to why sunscreen testing matters.

Ethylene glycol (EG) and diethylene glycol (DEG) are toxic industrial chemicals that have no place in consumer health products. Unfortunately, products ranging from cough syrups to dietary supplements have been found to contain these contaminants, often with tragic consequences.

Photostability testing is crucial for ensuring the safety, efficacy, and quality of products. While there are not specific requirements, the FDA makes it clear it is recommended for all products susceptible to light. Check out our infographic about the importance of photostability testing in OTC products.

As consumer demand for cleaner labels and naturally derived ingredients continues to rise, many manufacturers of OTC and dietary supplement products are reformulating to remove artificial colors and dyes. While this shift aligns with market trends, it introduces significant challenges—especially when it comes to product stability.

In this video, Business Unit Manager Ian Laessig shares how the Eurofins team collaborates with OTC and GMP clients to ensure compliant testing and a seamless experience.

In this video, Business Unit Manager Ian Laessig explores how Eurofins Food Chemistry Testing supports the OTC and GMP industries with comprehensive testing solutions for APIs in finished products, ingredients, and excipients.

Homeopathic formulations can be complex and challenging to test. A client approached Eurofins Supplement & OTC Testing in Madison, WI needing specialized testing of homeopathic tinctures. Read our case study to learn how the client was able to confidently release their product while maintaining compliance and efficiency.

The Food and Drug Administration (FDA) monitors drug manufacturers' compliance with its current Good Manufacturing Practice (cGMP) regulations in order to ensure the quality of drug products. These regulations are designed to assure products are safe for use and contain the ingredients, strengths, and efficacies of claims made by the product. Learn what tests your OTC products need to be compliant.

The world of wellness is experiencing a “gummification” wave, which includes using gummies to deliver APIs as a replacement for traditional forms like pills and syrups. But this matrix doesn't come without challenges. Click to read how you can ensure the effectiveness of alternative forms like gummies, chews, drink mixes, and lozenges.

This webinar explores approaches to method and monograph development while maintaining safety and quality standards specific to the OTC and Dietary Supplement industries. The speakers share industry insights regarding current state and potential changes with a changing administration. Original Air Date: February 24, 2025.