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  • Home
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      • Management Services Organizations (MSO) Issues
      • Technology Agreements
      • Telemedicine
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      • Cosmetics Claims
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      • Off-Label Use
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    • Firm Experience
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    • CHIROPRACTORS
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FDA Warns Foreign Maker of a Hand Sanitizer Product That Its Product is Adulterated
By Staff
In Healthcare Law
Posted August 15, 2021

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.

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Center for Food Safety and Applied Nutrition Sends a Strong Warning to CBD Product Manufacturer
By Staff
In Dietary Supplements (Claims and Labeling)
Posted August 1, 2021

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.

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FDA Warning Letters for Misbranding Cannabinoid Products as Dietary Supplement on the Rise – Bella Rose Labs
By Staff
In Dietary Supplements (Claims and Labeling)
Posted June 1, 2021

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

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Critical Legal Issues for the Cosmetics Industry: Interstate Commerce, Adulterated, and Misbranded
By Staff
In Cosmetics
Posted March 1, 2021

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.

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What Happens If You Make Cosmetic, OTC Drug, or Dietary Supplement with Hemp, Cannabis, or THC – Part Two
By Staff
In Cannabis Law
Posted December 22, 2020

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

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What Happens If You Make a Food with Hemp, Cannabis, or THC – Part One
By Staff
In Cannabis Law
Posted November 22, 2020

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

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FDA Issues Warning Letter to Company that Sells CBD Products Online and Through Social Media
By Staff
In Healthcare Law
Posted November 15, 2020

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.

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Why Medical Device Companies Need to Fear FDA Warning Letters
By Staff
In FDA & FTC Law
Posted November 1, 2020

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 [...]

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September 2020 FDA Warning Letters
By Staff
In FDA & FTC Law, Healthcare Law
Posted October 12, 2020

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.

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Red Flags that Leads to FDA Warning Letters
By Staff
In FDA & FTC Law
Posted September 1, 2020

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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FDA Warning Letters To Companies Claiming Products Boost Immunity and Treat COVID-19
By Staff
In Healthcare Law
Posted May 9, 2020

FDA Warning Letters To Companies Claiming Products Boost Immunity and Treat COVID-19

Federal Drug Administration continues to send warning letters to companies that boast products can treat, diagnose, prevent, or cure COVID-19 or boost immunity.

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New Farm Bill Opens Up Opportunities for the CBD Oil Market- If Companies Comply with the Legal and Regulatory Requirements
By Staff
In FDA & FTC Law
Posted February 8, 2020

New Farm Bill Opens Up Opportunities for the CBD Oil Market- If Companies Comply with the Legal and Regulatory Requirements

The Farm Bill of 2018 legalized CBD products that are hemp based for certain pharmaceutical uses. Food and dietary supplement possibilities may follow. Many different federal and state laws and [...]

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