Tag: Fda regulation

While many first aid products are readily available, potent hemostatic agents like thrombin are strictly controlled. **Is thrombin over the counter?** The clear and unequivocal answer is no, due to the serious health risks associated with its use and the need for medical supervision during administration.

According to a 2023 survey, nearly 75% of Americans take at least one dietary supplement, yet extensive research shows little to no benefit for healthy individuals with a balanced diet. This raises a critical question: **Do supplements actually work or just a have?** The answer is more nuanced than simple yes or no, depending on the specific supplement, the individual's needs, and the available scientific evidence.

According to the National Institutes of Health, many Americans do not get sufficient amounts of essential nutrients from diet alone. This often leads to the question, 'Are prescription vitamins better than over-the-counter?' and the answer depends heavily on your individual health needs and the regulatory differences that affect product quality.

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.

Did you know that many popular oral decongestants sold over-the-counter are largely ineffective? Following extensive review, the FDA announced in late 2024 that it is proposing to remove medications containing oral phenylephrine, an ingredient found in numerous cold and allergy products, because it has been proven to be no better than a placebo for nasal congestion.

Clinical trial data for brand-name tirzepatide (Zepbound, Mounjaro) shows that patients may begin to experience appetite suppression within the first 1-2 weeks, but for compounded tirzepatide, the timeline can be less predictable and is impacted by formulation variances.

While compounded semaglutide contains the same active ingredient as FDA-approved versions, it is not an identical or equivalent product. Its quality, safety, and effectiveness are not subject to the rigorous testing and review mandated by the FDA for branded medications like Ozempic and Wegovy.

In the United States, an estimated 122 million people use eyedrops [1.7.2]. But a common question remains: are eyedrops considered a drug? Legally, the answer is yes; all eyedrops are regulated as drugs by the U.S. Food and Drug Administration (FDA) [1.2.1].

With over 75 years in operation, Solgar is a well-established name in the supplement industry, respected for its commitment to consistency and quality. However, in a largely unregulated market, consumers must ask, 'Are Solgar supplements safe?' and look beyond a brand's reputation to assess its overall reliability.

According to reports, poison control center calls related to kratom exposure increased tenfold between 2010 and 2015, highlighting a pressing public health concern and prompting the critical question: is kava safer than kratom?. Both plant-based substances, often used for their psychoactive effects, carry distinct and significant safety profiles that consumers need to understand before use.