While feminine wash products are labeled for “external use,” FDA should recognize that they are used internally by consumers and adjust relevant colorant restrictions accordingly, the congresswoman suggests in a letter to agency Commissioner Robert Califf. The New York Democrat presses FDA to respond to a year-old citizen petition on the matter from NGO Women’s Voices for the Earth.
FDA should prohibit manufacturers from “mischaracterizing” feminine-wash products as “for external use only” and alter its colorant regulations to reflect common consumer practices of using the products internally, according to Rep. Grace Meng, D-N.Y.
In a Nov. 1 letter to FDA Commissioner Robert Califf, she advances the argument that feminine-wash products are...
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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