FDA amends food additive regulations with Oakshire’s petition to use agaricus bisporus mushroom powder, produced using UV light treatment, as a source of vitamin D2 in foods and supplements.
Oakshire Naturals LP’s proposal to allow using vitamin D2 mushroom powder in food and dietary supplements has the US Food and Drug Administration’s approval less than 3 months after the Pennsylvania firm received the European Union’s clearance for a similar proposal.
The FDA on 10 July published a Federal Register notice announcing its acceptance of Oakshire’s food additive petition to...
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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