FDA Warns Foreign Maker of a Hand Sanitizer Product That Its Product is Adulterated

The Food and Drug Administration issued a warning letter to a foreign manufacturer that the substation of methanol for ethanol rendered its produce a new drug, adulterated, and misbranded.

Center for Food Safety and Applied Nutrition Sends a Strong Warning to CBD Product Manufacturer

Center for Food Safety and Applied Nutrition sends FDA warning letter to CBD manufacturer of products for adults and kids – for adulteration/misbranding FD&C Act violations.

FDA Warning Letters for Misbranding Cannabinoid Products as Dietary Supplement on the Rise – Bella Rose Labs

FDA issues warning letter to New York manufacturer for CBD claims that indicates its products are new drugs and do not qualify as dietary supplements

Critical Legal Issues for the Cosmetics Industry: Interstate Commerce, Adulterated, and Misbranded

Cosmetics are regulated by the Food, Drug, and Cosmetic Act. FDA’s primary focus on whether the cosmetics have been adulterated or misbranded.

What Happens If You Make Cosmetic, OTC Drug, or Dietary Supplement with Hemp, Cannabis, or THC – Part Two

Healthcare makers, distributors, and sellers must comply with FDA rules and warning letters for their cannabis, hemp, and THC products including foods, OTC drugs, cosmetics, and dietary supplements

What Happens If You Make a Food with Hemp, Cannabis, or THC – Part One

Healthcare makers, distributors, and sellers must comply with FDA rules and warning letters for their cannabis, hemp, and THC products including foods, OTC drugs, cosmetics, and dietary supplements

FDA Issues Warning Letter to Company that Sells CBD Products Online and Through Social Media

FDA sends warning letter to a company because its website and social media accounts made claims about CBD products that suggest they are drugs or dietary supplements and were misbranded.

Why Medical Device Companies Need to Fear FDA Warning Letters

The FDA examines whether medical devices comply with the regulations of the Food, Drug, and Cosmetic Act. Two of the most common violations medical device companies are charged are adulteration [...]

September 2020 FDA Warning Letters

FDA and FTC warning letters continue to find violations of the FD&C Act when companies boast their products can cure or treat diseases such as COVID-19.

Red Flags that Leads to FDA Warning Letters

The FDA issues warning letters for numerous products including dietary supplements. FDA violations include findings that the supplement is a new drug, product adulteration, misbranding, and [...]

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