OTC Medicines

(JACKSON, Miss) – The Consumer Healthcare Products Association (CHPA) applauds Mississippi Representative Stacey Wilkes, Senator Hob Bryan, and Governor Tate Reeves for passing and signing legislation into law requiring all manufacturers of over-the-counter (OTC) medicines containing pseudoephedrine (PSE) to participate in supporting the costs and administration of the National Precursor Log Exchange (NPLEx) system – a real-time stop-sale technology that allows retailers to enforce PSE sales limits and assist law enforcement in preventing illegal PSE sales. This important step not only strengthens the NPLEx system overall, but it enhances its long-term viability in preventing illegal sales of medicines containing PSE in Mississippi.

“CHPA and its member companies look forward to working with Secretary Kennedy to advance policies that will enhance American consumers’ access to safe, effective, and affordable self-care options. With a growing demand for OTC medicines, dietary supplements, and OTC medical devices, it is imperative that our nation’s healthcare leaders expand access, streamline regulatory pathways, and reinforce public confidence through transparent, data-driven decisions. This can be achieved through the reauthorization of the Over-the-Counter Monograph Drug User Fee Program (OMUFA), Rx-to-OTC switch improvements, and the modernization of the more than 30-year-old Dietary Supplement Health and Education Act (DSHEA).

(WASHINGTON, D.C.) – Consumer Healthcare Products Association (CHPA) President and CEO Scott Melville released the below statement following President Trump imposing a 25% tariff on imports from Mexico and Canada, which were originally set to take effect Tuesday, Feb. 4 at 12:01 a.m. EST. As of this morning, the Trump Administration has agreed to pause sweeping tariffs on Mexico for one month while the two sides work on an agreement.

The Consumer Healthcare Products Association (CHPA) today announced the recent hiring of Dr. Fred Meadows as its new Senior Director of Quality, Technical, and Regulatory Affairs and Dr. Caitlin Ondracek as its new Senior Director of Medical Science and Regulatory Affairs. Meadows will report to Dr. Marcia Howard, Vice President of Regulatory and Scientific Affairs, and Ondracek will report to Dr. Jay Sirois, Vice President of Regulatory and Scientific Affairs.

The Consumer Healthcare Products Association (CHPA) released a statement following the U.S. Food and Drug Administration (FDA) issuing a final rule for Nonprescription Drug Product With an Additional Condition for Nonprescription Use (ACNU).