Anna Benevente, director of the Product, Labeling and Ingredient Review Department at consultancy Registrar Corp, offers perspective on the US FDA’s overdue rulemaking proposal for fragrance allergen labeling on cosmetic products under MoCRA, as well as adverse event reporting compliance.
The US Food and Drug Administration may issue a proposed rule for fragrance allergens labeling under the Modernization of Cosmetics Regulation Act in October after missing the statutory June deadline, with expectations for a 1-2 year transition period before disclosures are required.
“All we know at this point is the proposed list is coming out in October potentially – that’s what was...
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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