The agency plans to respond by March 30 to the Environmental Working Group’s 2011 citizen petition requesting regulatory action on hair-straightening products that contain or release formaldehyde. In doing so, it could win dismissal of a related suit filed by the NGO and put marketers on notice about regulatory measures that either are, or are not, coming their way.
A suit filed against FDA in Washington, D.C. District Court by the Environmental Working Group and Women’s Voices for the Earth could have implications for marketers of hair smoothers that contain or release formaldehyde, with the agency’s official word on such products potentially in sight.
EWG lodged a citizen petition with FDA in April 2011 asking the agency to investigate deceptive marketing and labeling practices...
Green Pharmaceuticals’ SnoreStop Nasal Spray, previously marketed as “NasoSpray,” still is available even though agency officials on multiple occasions for a month recommended a recall after an April inspection found “gross microbial contamination” in one lot.
In this episode of the Over the Counter podcast, HBW Insight speaks to Kerry's RDA senior manager of immune and joint health, Sonja Nodland, about the opportunity for innovation that postbiotics represent for the consumer health industry.
Week after publishing safety alert about OPMS Black Liquid Kratom “linked to serious adverse health effects, including death,” FDA announced market research “to understand and characterize emergent risk/safety and perceived benefits reportedly linked to kratom and psychedelics.” But it withdrew the study 10 days later.
Height of plaintiff attorney’s argument to present evidence which would prompt speculation by a jury was request to parse research by Kenvue’s lead expert, who coordinated the International Consensus Statement on ADHD by the World Federation of ADHD, where he’s president.
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