Tag: Consumer health

Over 500 million prescriptions are filled annually in the United States, leading many people to encounter the need for pill identification. The seemingly simple question, 'What pill is p10?', is surprisingly complex, as this imprint can belong to several different medications, each with its own purpose and side effects. Correctly identifying a pill based on its imprint, shape, and color is crucial for patient safety.

According to the National Center for Complementary and Integrative Health (NCCIH), the use of probiotics by U.S. adults quadrupled between 2007 and 2012. While their popularity soars, the key question remains: are there any FDA approved probiotics? The answer involves a critical distinction in how the FDA regulates products based on their intended use, a fact often misunderstood by consumers.

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.

Each year, U.S. poison centers report approximately 9,000 to 11,000 exposures to camphor, primarily involving accidental ingestion by young children [1.7.1]. This statistic highlights the importance of understanding the regulations surrounding this common compound. So, is camphor legal in the US? The answer is yes, but with significant restrictions.

First approved by the FDA in 1958, dextromethorphan (DXM) has long been a common ingredient in over-the-counter cough suppressants. With a variety of Robitussin formulations available, many wonder: **Does Robitussin still contain dextromethorphan?** The answer is that it depends on the specific product, as Robitussin is a brand name for a line of medications, not a single one.

In November 2022, a specific batch of a Vicks product was recalled in Australia, sparking widespread concern about the popular cough suppressant. This recall was not due to a widespread product defect but stemmed from a critical labeling error that caused potential health risks for consumers who unknowingly purchased the wrong formula. This article delves into the details of the Australian Vicks VapoRub recall, clarifying the reasons behind it and reinforcing general medication safety practices.

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 the U.S. Food and Drug Administration (FDA), a robust, multi-stage evaluation process is required before a new drug can be approved for sale. Knowing how to know if a medication is FDA approved is a critical step for patients and consumers to ensure the safety and effectiveness of the products they use.

In September 2023, a U.S. Food and Drug Administration (FDA) advisory committee unanimously voted that oral phenylephrine is not an effective treatment for nasal congestion. This has led to the FDA's proposed removal of the ingredient, leaving many to wonder what nasal decongestant is FDA removing and what options are available for relief.

The U.S. Food and Drug Administration (FDA) does not approve dietary supplements for safety or effectiveness before they are marketed. This critical distinction is key when asking, 'Is Recell supplement FDA approved?', as there is public confusion between a legitimate, FDA-approved medical device called the RECELL® System and unapproved products marketed as supplements.