Food and Drug Administration

The FDA is the US Government Agency that is supposed to help the public by regulating dangerous products and warning the public of any dangers caused by anything sold or consumed in the US.

Learn more about the FDA, is role and responsibilities and how they are designed to help you make informative decisions on the products that you place in and on your body.

Who is the FDA?
The Food and Drug Administration (FDA) is a federal agency of the United States Department of Health and Human Services (HHS). Its primary mission is to protect public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, food supply, cosmetics, and products that emit radiation. The FDA also plays a significant role in advancing public health by helping to speed innovations that make medicines and foods more effective, safer, and more affordable.

When Was the FDA Founded?
The FDA was founded in 1906 with the passage of the Pure Food and Drugs Act. This act was a response to widespread public concern about the safety and labeling of food and drugs, highlighted by Upton Sinclair’s novel “The Jungle,” which exposed unsanitary conditions in the meatpacking industry. Over the years, the FDA’s scope and authority have expanded through various amendments and acts, making it a central figure in regulating products that affect public health.

Roles and Responsibilities
The FDA has several key roles and responsibilities, including:

Regulation of Drugs and Medical Devices: The FDA ensures that drugs and medical devices are safe and effective before they can be marketed. This includes rigorous testing, clinical trials, and review processes.

Food Safety: The FDA oversees the safety of the U.S. food supply, excluding meat, poultry, and certain egg products, which are regulated by the USDA. It sets standards, conducts inspections, and monitors foodborne illnesses.
Cosmetic Safety: The FDA regulates the safety of cosmetics, ensuring that they are free from harmful contaminants and are accurately labeled.

Radiation Protection: The FDA monitors products that emit radiation, such as X-ray machines and microwave ovens, to protect the public from excessive exposure.
Public Health Notifications: The FDA issues recalls, safety alerts, and other notifications to protect the public from potentially dangerous products.

Shortcomings of the FDA
Despite its critical role, the FDA has faced criticism for some decisions that have had adverse effects on public health:

Approval of Thalidomide: In the 1950s and 1960s, thalidomide was marketed as a safe drug for treating morning sickness in pregnant women. However, it led to severe birth defects. The FDA initially refused approval but later allowed limited use, leading to tragic consequences.
Slow Response to Vioxx: The FDA faced backlash for its delayed response in withdrawing the painkiller Vioxx from the market in 2004, which was found to increase the risk of heart attacks and strokes, resulting in thousands of deaths.
Regulation of E-Cigarettes: Critics argue that the FDA has been slow to regulate e-cigarettes and vaping products, leading to widespread youth addiction and health issues.

Positive Contributions of the FDA
The FDA has also made numerous positive contributions that have saved lives and improved public health:

Polio Vaccine Approval: The FDA’s rigorous testing and approval of the polio vaccine in the 1950s helped eradicate the disease in the U.S., saving countless lives.

Food Safety Modernization Act (FSMA): Enacted in 2011, FSMA significantly improved food safety standards, focusing on preventing foodborne illnesses rather than just responding to them.

Orphan Drug Act: This act, passed in 1983, has facilitated the development and approval of drugs for rare diseases, providing treatments for conditions that previously had none.

Interaction with Other Government Agencies
The FDA collaborates with various other government agencies to enhance public safety:

Centers for Disease Control and Prevention (CDC): The FDA works with the CDC to monitor and control outbreaks of foodborne illnesses and infectious diseases.

Environmental Protection Agency (EPA): The FDA collaborates with the EPA to regulate pesticides and ensure that food and drug manufacturing does not harm the environment.

Department of Agriculture (USDA): The FDA and USDA work together on food safety, particularly in areas where their responsibilities overlap, such as the regulation of certain egg products.

References
FDA Official Website
History of the FDA
FDA Food Safety Modernization Act

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