Law360
A Weak Link In Consumers' FDA Test Claims
October 11, 2019
For certain consumer products, U.S. Food and Drug Administration regulations mandate specific testing procedures or methodologies that must be followed in order to make particular claims about the product’s features or use. These types of regulations cover, for example, over-the-counter monograph products, such as anti-cavity dental products or sun protection factor sunscreens. These types of regulations also cover nutrient content claims for foods and dietary supplements — everything from sugar content for cereals, to protein content in protein shakes, to vitamin content in supplements.
Contacts
Capabilities
Suggested News & Insights
Trend Watch 2026: Hot Topics in California Regulation and LitigationTuesday, February 10, 2026Sidley Clinches Victory in HEC AD/CVD InvestigationsJanuary 30, 2026Sidley Represents Glenfarne as Principal Project Counsel on Alaska LNGJanuary 29, 2026Sidley Advises Marathon Asset Management on its up to US$1.6 Billion Sale to CVCJanuary 26, 2026Sidley Advises on Market-Defining Cross-Border India Matters in 2025January 12, 2026New U.S. Executive Order Targets Stock Buybacks, Dividends, and Executive Compensation for Underperforming Defense ContractorsJanuary 9, 2026
- Stay Up To DateSubscribe to Sidley Publications
- Follow Sidley on Social MediaSocial Media Directory

