Category: Regulation

Over 200,000 different pharmaceutical products are estimated to be on the global market, yet the classification system for these substances can differ dramatically by region. Understanding **what is the meaning of schedule 6?** is a prime example of this variation, as its definition is highly dependent on the governing national or state regulations rather than a single, universal standard.

The term "superfood" has no official or legal definition from the Food and Drug Administration (FDA). This marketing term is used to promote foods with exceptional nutrient density, but it does not equate to the FDA approval process required for prescription drugs.

Caffeine is the most widely consumed psychoactive substance in the world, yet the question of **why isn't caffeine treated as a drug** with strict controls often arises, pointing to its unique legal and social status. While it fits the pharmacological definition of a drug due to its effects on the central nervous system, its regulatory path has been defined by its milder nature and cultural integration.

According to the U.S. Food and Drug Administration (FDA), every human drug product is assigned a unique, 3-segment, 10 or 11-digit number known as the National Drug Code (NDC). Understanding what does an NDC stand for is crucial for anyone involved in healthcare, from pharmacists to patients, as it serves as a universal product identifier across the U.S..

The U.S. Food and Drug Administration (FDA) has only approved one purified CBD drug for specific seizure conditions, named Epidiolex. This fact highlights the critical distinction between regulated medication and consumer products when answering the question: **Do CBD gummies count as drugs?**.

While the legality of cannabis has been a major topic of discussion in recent years, the retail landscape for kratom is significantly different, and the question, "Is kratom sold in dispensaries?" does not have a simple yes or no answer. In the United States, kratom is not federally regulated as a medication or dietary supplement, which results in a patchwork of state and local laws governing its sale and distribution.

According to the FDA, several mass-produced versions of progesterone, such as Prometrium and Endometrin, have been tested and approved for use in the United States. However, when considering the question, 'is progesterone legal in the US?', the answer depends heavily on the specific product, its manufacturing, and its intended use. The legal landscape varies significantly between FDA-regulated prescriptions, custom-made compounded treatments, and over-the-counter creams.

As of mid-2025, the U.S. Food and Drug Administration (FDA) has granted marketing orders for a limited number of electronic nicotine delivery systems (ENDS). This process, known as the Premarket Tobacco Product Application (PMTA) pathway, determines which vapes are FDA authorized for sale in the U.S., but it is crucial to understand that it is a marketing authorization, not an official safety endorsement.