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Entrenet Nutritionals, Inc.

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Entrenet Nutritionals, Inc.

According to a warning letter from the FDA, Entrenet Nutritionals is advertising four different nutritional supplements as drugs in violation of the Food, Drug, and Cosmetic Act because of the…

Mojo Risen

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Mojo Risen

The FDA is advising consumers to avoid Mojo Risen, a supplement sold for sexual enhancement, as it contains an unlisted drug ingredient. In laboratory analysis, the FDA “confirmed that ‘Mojo…

Code Red Seven

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Code Red Seven

This radio ad for a product called Code Red Seven makes it sound pretty miraculous. “David” was suffering from decreased libido due to his unhealthy lifestyle, but apparently Code Red…

Y. S. Health Corp

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Y. S. Health Corp

The FDA has issued a warning letter to Y.S. Health Corp for making drug claims in violation of the Food, Drug, and Cosmetic Act. Y.S. Health Corp is also under…

Lisa Laser Products

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Lisa Laser Products

An FDA investigation into Lisa Laser Products for its Sphinx Laser Systems, FlexGuard, and Revolix Lasers found that these products were misbranded because they were not properly reported as medical…

Purus Labs, Inc

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Purus Labs, Inc

The FDA sent a warning letter to Formulife, Inc./Purus Labs, Inc., after the dietary supplement maker was found to be selling products containing DMAA, which has been banned by the…

Illegally Sold Diabetes Treatments

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Illegally Sold Diabetes Treatments

The FDA in July sent letters to 15 domestic and foreign companies telling them that their sale of diabetes treatments was illegal. The products, which had not been evaluated by…

Herbal Papaya

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Herbal Papaya

The FDA sent a warning letter to Herbal Papaya after the company promoted supplements with therapeutic claims on its website. Companies can’t make such claims about supplements without the FDA’s…

Reumofan

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Reumofan

USA TODAY published an investigation of popular arthritis supplement Reumofan this week — an investigation that found, basically, you want to stay away from Reumofan. [C]onsumers who buy Reumofan products…

Potiga

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Potiga

The FDA has warned consumers that anti-seizure medication Potiga can cause blue discoloration of the skin and pigment changes in the eye, and that pigment changes in the eye can…

SmartPractice

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SmartPractice

According to a warning letter from the FDA, the Danish company, SmartPractice, promoted an allergic contact dermatitis test kit called T.R.U.E. Test® without adequate potential risk information, including that the product…

Twiish

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Twiish

Acne ads targeting teens come under scrutiny.

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