Tag: Fda ban

In 1998, the U.S. Food and Drug Administration (FDA) declared Mercurochrome, a once-common household antiseptic, as "not generally recognized as safe and effective," effectively banning its sale in the U.S.. As a result, the answer to the question "Do doctors still use Mercurochrome?" is a definitive no, as medical professionals now rely on safer and more effective modern alternatives for wound care.

In 1998, the U.S. Food and Drug Administration (FDA) effectively halted the sale of mercurochrome in the United States due to concerns over its mercury content [1.4.1, 1.7.2]. Consequently, if you're asking, 'Does Walmart sell mercurochrome?', the answer is a clear no.

In 2004, the U.S. Food and Drug Administration (FDA) banned the sale of dietary supplements containing ephedrine alkaloids from the *Ephedra* plant after linking them to serious health risks like heart attack and stroke. However, the legality of the *Ephedra* plant itself is more complex, with specific regulations based on the plant species and how it is sold and used.

In 2004, the U.S. Food and Drug Administration (FDA) banned the sale of dietary supplements containing ephedrine alkaloids due to serious health risks, which fundamentally changed where one can find Ephedra and its related products. This regulatory action followed thousands of adverse event reports, including heart attacks, strokes, and death.

On February 21, 2025, the U.S. Food and Drug Administration (FDA) officially declared the national shortage of Ozempic and Wegovy resolved, triggering a cascade of regulatory actions that directly impact what will happen to compounded semaglutide. This decision has led to a major crackdown on compounding pharmacies that have been producing unauthorized versions of the popular weight-loss and diabetes medication.

In 2016, the FDA banned triclosan from consumer antiseptic wash products after manufacturers failed to prove it was both safe for daily use and more effective than plain soap and water. Understanding the side effects of triclosan soap is crucial for making informed choices about personal care products.

The U.S. Food and Drug Administration (FDA) recommends that consumers do not use any products containing phenylpropanolamine due to its association with an increased risk of hemorrhagic stroke. Therefore, the question of **how many days should I take phenylpropanolamine?** is moot, as it is no longer available for human use in the U.S..

The US Food and Drug Administration (FDA) issued a public health advisory in 2000, requesting manufacturers voluntarily discontinue marketing products containing Phenylpropanolamine (PPA), including PPA drops. Once a common ingredient for nasal congestion and appetite control, PPA's human use was phased out due to serious safety concerns, namely an increased risk of hemorrhagic stroke. However, the compound still has limited, specific uses in veterinary medicine.

In early 2025, the FDA officially declared the semaglutide shortage resolved, a decision with profound implications for the thousands of patients relying on compounded versions. This move triggered a ban on the widespread production of these non-FDA-approved drugs, fundamentally changing the landscape for those asking, 'will compounded semaglutide go away?'.

In 2000, the U.S. Food and Drug Administration (FDA) issued a public health warning and subsequently requested that manufacturers stop marketing products containing phenylpropanolamine (PPA), effectively banning its sale due to a link to an increased risk of hemorrhagic stroke. Therefore, the answer to the question, 'Can I take phenylpropanolamine and cetirizine together?', is a definitive **no**, due to the serious safety risks associated with PPA. This guide explains why this combination is dangerous and outlines the safer, modern alternatives for treating cold and allergy symptoms.