UMA Oils must lose claims on its skin- and hair-care products regarding acne and eczema treatment, among others, if it intends to continue marketing them as cosmetics, FDA says in a July warning letter. The company touts its offerings as based on ancient Ayurvedic principles and five generations of family expertise.
Vedame Oils, LLC may market handcrafted oils for face, hair and body based on centuries-old Ayurvedic practices, but the standard for cosmetic claims remains the 1938 Food, Drug and Cosmetic Act, as underscored by FDA's July 18 warning letter to the company.
"The claims on your website establish that these products are drugs … because they are intended for use in the...
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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