Efforts to unite as an industry to provide the US Food and Drug Administration with data to fill safety gaps for “chemical” UV filters have fizzled as the agency insists on animal-test requirements. Without a collaborative effort to share resources and costs, the long-marketed sunscreen actives may not receive the investment needed to demonstrate GRASE, and the US market may decay further in comparison with the diversity of modern sun-protection options available to consumers abroad.
An industry collaborative comprising more than 20 sunscreen product manufacturers and ingredient suppliers is no longer working to fulfill data needs identified by the US Food and Drug Administration for seven sunscreen UV filters currently on the market due to concerns over agency requirements for animal-based tests to support safety.
What that means for the future of those sunscreen active drug ingredients and the sunscreen products category in the US...
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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