Cosmetic Ingredient Review’s independent expert panel needs more data to assess the safety of prostaglandin analogs, but ultimately may pass review back to the US Food and Drug Administration due to concerns that the substances impact the structure and function of the body and thus are unapproved drugs with potentially serious side effects.
The Expert Panel for Cosmetic Ingredient Safety wants to see data that demonstrate prostaglandin analogs used in cosmetic products do not elicit effects that would identify them as drugs, adding to a long list of information it needs to review as it assesses the ingredients’ safety.
As drug safety is outside the panel’s remit, Cosmetic Ingredient Review has asked its independent experts to focus just on...
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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