Tag: Consumer safety

In 2009, the European Union banned the importation of consumer products containing dimethyl fumarate (DMF) following widespread reports of severe skin reactions, a condition dubbed 'toxic sofa dermatitis'. This critical regulatory action is a key reason **why is DMF banned** in certain applications, despite a delayed-release formulation of the compound being approved for medical use.

The CBD market was valued at $18 billion in 2022 and is projected to more than triple in the next decade, with many consumers wondering, **can you buy CBD products over the counter**? The answer is complex, hinging on federal law, state regulations, and a notable lack of FDA oversight for most retail products.

Less than 1% of dietary supplements are subject to mandatory pre-market review by the FDA, a process required for prescription drugs. This regulatory distinction is key to understanding what the FDA says about Nugenix, an over-the-counter testosterone booster.

In 2025, several over-the-counter (OTC) cold medications have been recalled for reasons ranging from contamination to packaging defects [1.2.4, 1.3.2]. This article details which cold medicine was recently recalled, the reasons why, and what consumers need to know to stay safe.

Since 2023, the FDA has coordinated several eye drop recalls impacting numerous brands due to serious contamination and manufacturing issues. This article provides a crucial breakdown of **what brands of eye drops are recalled** and why, to help protect your eye health.

In recent years, the U.S. Food and Drug Administration (FDA) has overseen the recall of dozens of over-the-counter eye drop products, raising consumer concerns [1.5.1]. This environment of heightened scrutiny leads many to ask: **Has Refresh eye drops been recalled?**

In 2006, the Combat Methamphetamine Epidemic Act was signed into law, which fundamentally changed how consumers purchase cold and allergy medicines. Many people mistakenly believe **why was pseudoephedrine taken off the market**, but the reality is more nuanced; the medication was not removed but was heavily restricted due to its use in manufacturing illegal methamphetamine.

According to the official Tiger Balm website, all Tiger Balm products sold in the U.S. comply with the regulations of the U.S. Food and Drug Administration (FDA). This means that, when manufactured and labeled correctly, **is Tiger Balm legal in the USA?** Yes, it is a legal and widely available over-the-counter medication.

More than half of American adults use dietary supplements, often believing they are FDA-regulated and tested for safety, which is not true. For those considering a brain health product, understanding **what are the side effects of Prevagen?** is crucial, especially given the history of consumer complaints and limited scientific evidence.

The pivotal Durham-Humphrey Amendment of 1951 legally separated drugs into two classes: prescription and nonprescription, providing the foundation for modern drug classification. This crucial distinction is the root of the naming convention, addressing the question: **Why are they called OTC drugs?**