FDA’s draft guidance setting a 10ppm limit on trace lead in cosmetic products is not protective enough, according to stakeholders, including Beautycounter, which bills itself as “a company devoted to progress.” Commenter recommendations range from lowering the ceiling to banning lead-contaminated products outright.
Beautycounter recognizes that trace lead in cosmetic products is a practical reality that can’t be avoided entirely, but the direct sales and e-commerce company joins a host of consumer advocacy groups in asking FDA to reconsider its recommended 10 parts-per-million lead limit for cosmetic products.
“It is our opinion that the limit of 10ppm for lead in color cosmetics is too high given the scientific...
Devices authorized for marketing outside the US. Data derived from Citeline’s Meddevicetracker. Updated weekly.
PATIENT ACCESS TO UNAPPROVED MEDICAL PRODUCTS WOULD BE ALLOWED under legislation introduced by Rep. Peter DeFazio (D-Ore.) on July 12 and Sen. Tom Daschle (D-S.D.) on July 14. Called the Access to Medical Treatment Act, the legislation would allow health practitioners to administer unapproved drugs, devices, foods or dietary supplements to patients as long as there is no evidence the treatment causes harm and the patient is informed about the treatment and its possible side effects. DeFazio's bill is identified as HR 2019; Daschle's version will be assigned a bill number the week of July 17.
A look at new research on the cardiovascular effects of ADHD medications and what it means for clinical care. This article explores the latest clinical and epidemiological research on the cardiovascular effects of medications commonly prescribed for ADHD, examining potential heart-related risks, underlying mechanisms, and their implications for patient safety, clinical decision-making, and long-term treatment strategies across diverse age groups and risk profiles.
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