This product, when used as directed, produces an industrial bleach that can cause serious harm.

Swallowing doses of this bleach, such as those recommended in the labeling can cause nausea, vomiting, diarrhea, and symptoms of severe dehydration. (more…)

Silymarin (Silybium marianum), an extract of milk thistle, is often used to treat chronic liver disease.

Researchers with the Silymarin in the NASH and C Hepatitis (SyNCH) Study Group studied its effect when combined with interferon. (more…)

FDA is warning consumers that Reumofan Plus, marketed as a natural dietary supplement for pain relief and other serious conditions, contains several active pharmaceutical ingredients not listed on the label that could be harmful.

Here’s what we know. (more…)

Man Up Now claims to be “herbal” and “all natural.” Consumers may mistakenly assume the product is harmless and poses no health risk. One consumer below thinks it no big deal.

Consumers who have Man Up Now capsules should stop using them, because the FDA determined it contains sulfoaildenafil, a chemical similar to sildenafil, and the active ingredient in Viagra. (more…)

The FDA tells us that Wholistic Herbs Inc. is recalling all of its “Koff & Kold” spray with herbal extract and “Kold Sore” spray with liquid sea mineral. (more…)

According to the FDA, RegenArouse (Lot 130100) contains tadalafil (Cialis), an FDA-approved drug used as treatment for male erectile dysfunction, making this product an unapproved new drug. (more…)

This is the first time FDA has taken legal action against a dietary supplement manufacturer (ATF Fitness Products) of this size for failure to comply with the dietary supplement current Good Manufacturing Practice (cGMP) regulations. (more…)

FDA has recalled Pentrexyl Forte Natural because the packaging is believed to be misleading — causing it to be confused with an antibiotic.

(more…)

The FDA and the Federal Trade Commission (FTC) today announced a joint effort to remove products from the market that make unproven claims to treat, cure, and prevent sexually transmitted diseases (STDs).

Among the products targeted are Medavir, Herpaflor, Viruxo, C-Cure, and Never An Outbreak. (more…)

FDA is warning companies to stop making MRSA claims.

Methicillin-resistant Staphylococcus aureus (MRSA) bacteria can cause an infection that’s highly resistant to some antibiotics. MRSA cause infection after they enter the body through a cut or sore.

The US Food and Drug Administration has issued 4 warning letters to companies that manufacture and market over-the-counter (OTC) drug products (including hand sanitizers) that claim to prevent infection by MRSA. (more…)

FDA lab analysis of X-Hero found the product contains sulfosildenafil, the analogue of the active ingredient of an FDA-approved drug (sildenafil, Viagra, Revatio) used to treat erectile dysfunction.

In addition, FDA analysis of Male Enhancer found it contains tadalafil (Cialis, Adcirca), the active ingredient of an FDA-approved drug used to treat erectile dysfunction. (more…)

Being overweight after breast cancer treatment may increase a woman’s risk for recurrent disease.

Researchers at the University of Arizona, in Tucson found that there are benefits from drinking green tea, but weight loss isn’t one of them. (more…)

FDA has received reports of adverse events associated with the use of Fruta Planta, including several cardiac events and one death.

In addition, FDA testing revealed that certain lots of RockHard Weekend and Pandor contain an analogue of sildenafil, an FDA-approved drug used as treatment for male erectile dysfunction. (more…)

There are “significant public health problems posed by products that are marketed as dietary supplements but that contain the same active ingredients as FDA-approved drugs… that do not qualify as dietary ingredients.” (more…)

The FDA tells us that Vigor-25, a product marketed as a natural dietary supplement to enhance male sexual performance, should not be purchased or used because it contains sildenafil, the active ingredient in the prescription drug Viagra.

The FDA is investigating the reported death of a 26-year old man, possibly associated with the use of Vigor-25. (more…)

8 companies of over-the-counter (OTC) chelation products were told that they are selling unapproved drugs and devices and are violating federal law with respect to unproven claims about these products.

These products purport to treat a range of diseases by removing toxic metals from the body. Some also claim to treat autism spectrum disorder, cardiovascular diseases, Parkinson’s disease, Alzheimer’s disease, macular degeneration, and other serious conditions. (more…)

The FDA is taking action to prevent Rising Sun Health and The Center for Complimentary and Alternative Health of Livingston, Montana, from manufacturing and selling unapproved new drugs and adulterated or misbranded dietary supplements in violation of the law.

Rising Sun manufactured and distributed a variety of unapproved new drugs under names such as Black Salve, Cancema, and Can-Support. (more…)

So good they had to name it “slimming” twice.

Unfortunately, Slimming Beauty contains the active pharmaceutical ingredient sibutramine (Meridia), a stimulant. And the marketer, Beautiful Health Inc., formerly LL Health and Beauty, failed to list it among the ingredients on the label. (more…)

Aromatase inhibitors are a class of drugs used to treat breast cancer and ovarian cancer in postmenopausal women.

Now, the FDA is recalling the following supplements that illegally contain these drugs. (more…)

It’s labeled as “100% natural” and consumers may mistakenly assume the product is harmless and poses no health risk.

The FDA says, Not so fast, all you erectilely challenged people out there. (more…)