
- Fall 2011
- Volume 10
- Issue 3
Don’t Believe Everything You Read on Supplement Labels
Key Takeaways
- FDA oversight generally does not require premarket verification of supplement safety, efficacy, or label accuracy, unlike pharmaceuticals, increasing variability in product quality and content.
- Lack of standardized definitions for common claims such as “natural” shifts decision-making to labels that may not reflect bottle contents.
Cancer patients and survivors should discuss supplement and vitamin use with their oncologists.
The Food and Drug Administration treats dietary supplements more like food than drugs. This means that the standards the agency applies to medicines, including testing of products before they are put on the market, don’t apply to supplements. There is also no defined standard for many commonly used terms, such as “natural,” which means that consumers are often left to choose supplements based on the label—with no guarantee that what’s on the label is actually in the bottle.
Buyer, beware. Do some homework before buying supplements. For example, the service
Also, look for certain designations on the label that show the manufacturer has voluntarily subscribed to higher manufacturing practices. Several organizations offer independent verification, and if the products meet those standards for purity, quality and potency, a seal will appear on the label. For instance, U.S. Pharmacopeia has a verification mark (visit
Articles in this issue
almost 15 years ago
From Our Archives: Imagingalmost 15 years ago
Supplements During Cancer: Help or Hype?almost 15 years ago
Unlocking the Mystery of Cancer Stem Cellsalmost 15 years ago
Advocates Make Cancer Their Missionalmost 15 years ago
Choosing an Imaging Testalmost 15 years ago
Do You Need a Cancer Coach?almost 15 years ago
Coordinating Care After Canceralmost 15 years ago
How to Manage Family Dynamics During Canceralmost 15 years ago
Another State Gets Chemo Parityalmost 15 years ago
Ford Led Discussion on Breast CancerNewsletter
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