Discover your next big idea for life sciences at PACK EXPO Las Vegas
Experience a breakthrough in life sciences packaging—explore solutions from 2,300 suppliers spanning all industries, all in one place this September

USP urges consumers to consider the quality of their herbal products

As people in the U.S. become more aware of the purported health benefits of herbal products, it is important to consider their quality and their interactions with prescription and over-the-counter medicines people currently take for their aliments.

This content was written and submitted by the supplier. It has only been modified to comply with this publication’s space and style.

That is the recommendation of the U.S. Pharmacopeial Convention (USP), a nearly 200-year-old organization of technical and scientific experts that develops quality standards for medicines and their ingredients, food ingredients, dietary supplements and herbal medicines.

“Consumers often assume, incorrectly, that they do not need to worry because herbal products are ‘natural’ and that equals ‘safe’,” says Gabriel Giancaspro, Ph.D., vice-president for foods, dietary supplements and herbal medicines at USP. “Many herbal products may interact with other medications, increasing or decreasing their effect or causing adverse effects. Some toxic plants may be easily confused with those known to be safe, highlighting the importance of identity standards. In addition, purity standards are important to avoid contamination with microorganisms and toxic substances such as heavy metals. Variability in plant origin, source conditions and processing practices greatly impact overall quality.”

Data from a recent study from the Military Nutrition Division of the U.S. Army Research Institute of Environmental Medicine (USARIEM) indicates that as many as one in three adults in the U.S. take dietary supplements in combination with prescription drugs. USP urges consumers to always consult with their physicians on the use of herbal products and their potential side effects when combined with other medicines.

Consumers must also understand that while many countries have specific regulations for herbal or traditional medicines, the United States does not. Products that include a claim to treat or cure a disease are considered a drug by the U.S. Food and Drug Administration (FDA), but only a few herbal medicines have gone through the stringent process for drug approval. In most cases, herbal products are sold as dietary supplements or food ingredients, which do not require the same approval process.

“Public standards for quality of dietary supplements are not mandated, so the quality of herbal products sold as dietary supplements may vary significantly from one manufacturer to another”, says Giancaspro. Identity, purity and content standards such as the ones set by USP establish a common ground for quality of dietary supplements, but these should not to be confused with standards for safety or efficacy.”

For more information on USP’s quality standards for dietary supplements, visit: http://www.usp.org/dietary-supplements/dietary-supplements-compendium

Researched List: Blister Machines for Life Sciences
Need a blister machine for life sciences packaging? Our curated list features companies serving pharmaceutical, medical device, nutraceutical, and cosmetic industries. Download to access company names, locations, machine specifications, descriptions, and more.
Download Now
Researched List: Blister Machines for Life Sciences
Pharmaceutical Innovations Report
Discover the latest breakthrough packaging technologies shaping the pharmaceutical sector. This report dives into cutting-edge innovations, from smart containers that enhance patient safety to eco-friendly materials poised to transform the industry’s sustainability practices. All from PACK EXPO. Learn how forward-thinking strategies are driving efficiency and redefining what’s possible in pharma packaging.
Learn More
Pharmaceutical Innovations Report