Preview

Dietary Supplements Essay

Good Essays
Open Document
Open Document
643 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Dietary Supplements Essay
Congress drops the ball with supplement legislation Major corporations elude the Food and Drug Administration regulations. Manufactures that produce energy drink supplements have caused addiction and a worldwide epidemic on the belief that their product will give more energy. The first manufacture of energy drinks started in the early 1960’s in Japan with the introduction of Lipovitan D by a company called Taisho (Engber Daniel). In October 25, 1994 President Clinton signed into law, the Dietary Supplements Health and Education Act. The FDA cannot regulate dietary supplements as food. People of all ages have started to abuse and mix theses supplement drinks with alcohol trying to get a greater effect. On October 25, 1994 President Clinton signed into law the Dietary Supplements Health and Education Act. This legislation restricted how the FDA monitors Dietary Supplements. The FDA no longer has control on supplements and how they are sold to the public (The new dietary supplements law). The DSHEA says, if it is a vitamin, mineral, herb, botanical, or an amino acid and is intended to increase dietary supplement intake it constitutes as a supplement. “According to DSHEA, a dietary supplement is a product that is labeled as a dietary supplement and is not …show more content…
Corporations can now add this statement on their products, “This statement has not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease” (Commission on Dietary Supplement Labels). Allowing this, this will open doors for corporations allowing them to bypass regulations that were put in place to help protect people from harmful substances. Abuse of these substances could lead to serious health issues heart disease, high blood pressure, other serious health risk, or even

You May Also Find These Documents Helpful

  • Satisfactory Essays

    Hcs/ 490 Outline

    • 475 Words
    • 2 Pages

    References: Division of Drug Marketing, Advertising, and Communications (DDMAC). 2010. Retrieved August 6, 2010 from http://www.fda.gov/AboutFDA/CentersOffices/CDER/ucm090142.htm Food and Drug Administration (2010). Division of Drug, Marketing, Advertising, and Communications. Retrieved from http://www.fda.gov/AboutFDA/CentersOffices/CDER/ucm090142.htm Us Food and Drug Administration. (2010). Retrieved August 9, 2010 from website: http://www.fda.gov/AboutFDA/WhatWeDo/default.htm US Food and Drug Administration (2010). “Inspection, Compliance, Enforcement and Criminal Investigations.” Retrieved August 16, 2010 from www.hhs.gov.…

    • 475 Words
    • 2 Pages
    Satisfactory Essays
  • Powerful Essays

    50 NCLEX Q S EXAM 2

    • 3243 Words
    • 13 Pages

    A All dietary supplements are controlled by the FDA and thus are deemed safe and effective.…

    • 3243 Words
    • 13 Pages
    Powerful Essays
  • Powerful Essays

    and should not be labeled. Throughout the article Hemphill and Syagnik explain that the FDA is…

    • 1448 Words
    • 6 Pages
    Powerful Essays
  • Good Essays

    society, and is dangerous to all. Cherry supports the claim that everyone needs to stand-up to these companies to slow down the advertisements, and stop trying to shove pills down everyone’s throats.…

    • 1203 Words
    • 4 Pages
    Good Essays
  • Satisfactory Essays

    Sci/241 Supplements

    • 863 Words
    • 4 Pages

    There are also risks that occur with using dietary supplements that range from different levels and even things. In the United States dietary supplements are not watched and regulated as strictly as drugs are. Although…

    • 863 Words
    • 4 Pages
    Satisfactory Essays
  • Good Essays

    The impact of Food and Drug Act despite informal standards resulted in courts having different opinions. There were unique laws and specific standards established for foods such as apples, butter, and canned foods. In 1912, after the resignation of Wiley, the emphasis was on patent medicines. Although the law regarding drugs was clearer than foods in terms of standards, misbranding was still a concern.…

    • 741 Words
    • 3 Pages
    Good Essays
  • Satisfactory Essays

    Annotated Bibliography

    • 1543 Words
    • 7 Pages

    This scholarly article went into detail about the legal senses of FDA's rules on food labeling,…

    • 1543 Words
    • 7 Pages
    Satisfactory Essays
  • Good Essays

    The first energy drink was created in 1987 in Japan by a Japanese man named Dietrich Mateschitz. Mateschitz was the man who created the infamous energy drink, Red Bull. He got the concept of the energy drink from Taisho Pharmaceuticals in Japan, when they released a drink called Lipovitan-D that contained many ingredients that you see today in energy drinks. RedBull quickly became popular in Europe then spread around the world. The many ingredients in energy drinks are extremely dangerous. Caffeine, sugar, ginseng, guarana, ginkgo biloba, tauting, inositol, B vitamins, and antioxidants are just some of the ingredients in energy drink that, in large quantities, can be deadly.”(How exactly Do Energy Drinks...3). They are addicting and should not be consumed in large quantities.”One of the concerns in energy…

    • 543 Words
    • 3 Pages
    Good Essays
  • Powerful Essays

    The Food and Drug Administration, or FDA for short, is a government agency responsible for protecting the public health by assuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, our nation’s food supply, cosmetics, and products that emit radiation, and by regulating the manufacture, marketing, and distribution of tobacco products. The FDA is also responsible for advancing the public health by helping to speed innovations that make medicines and foods more effective, safer, and more affordable; and helping the public get the accurate, science-based information they need to use medicines and foods, and to reduce tobacco use to improve health (About FDA 1). I am deeply concerned about how the FDA is regulating food. In my opinion, the FDA is failing miserably with their duties to the citizens of the United States of America. They appear to be more interested in profit than with the overall well being of the public. They are allowing people to consume dangerous amounts of fluoride. Studies have shown that food additives are causing serious health related issues. I feel that the FDA needs a massive overhaul in their top-level leadership positions in order for them to improve.…

    • 1864 Words
    • 8 Pages
    Powerful Essays
  • Satisfactory Essays

    Hello, My name is Brittany N. Neal I'm a 27 year old single mother of 3. I'm currently employed as a dietary aid at a nursing facility I've been working there for a year. I also worked as a correctional officer at TDCJ for a year I liked the job just crazy work hours. i have a lot of experience in the nursing field I worked home health for years and I feel that I need to be certified its something that I love to…

    • 85 Words
    • 1 Page
    Satisfactory Essays
  • Powerful Essays

    Unjust FDA

    • 1784 Words
    • 8 Pages

    Your standing in line at your local drug store, head killing you, your face feels like it’s ready to explode, and you cannot breathe if your life depended on it. In short your allergies are making your life unbearable, and you are completely out of Sudafed. When you finally arrive at the pharmacist and ask for a box, you are asked for your driver’s license and then promptly turned away. Recent laws have you waiting one more week before purchasing anything that contains pseudoephedrine or ephedrine. Disgruntled and in pain, you walk away and as you leave the store you overhear the cashier tell a customer “instead of buying a pack a day, why don’t you just buy a carton?” Right about now the FDA’s “…goal of a healthier, safer nation…” ("Overview Of The FDA Mission", 2007) does not feel so accurate. The FDA’s regulations are unjust, because they place corporate profits above consumers’ safety, ban proven natural beneficial health medications, and allow the public’s lifestyle demands to alter their mission.…

    • 1784 Words
    • 8 Pages
    Powerful Essays
  • Good Essays

    Evaluation and Research,Center for Food Safety and Applied Nutrition, and National Center for Toxicological Research. This Agency was founded because of the Pure Food and Drug Act in 1906. The Pure Food and Drug Act was a law and it removed harmful foods and drugs. The responsibilities of the FDA was that it wanted to protect the public from harmful things that can harm the public. The FDA is an important part of the Federal Agency and the United States. The FDA is an important part of the federal government agency and United States.…

    • 526 Words
    • 3 Pages
    Good Essays
  • Powerful Essays

    The Dust Bowl

    • 2111 Words
    • 9 Pages

    The decade that became known as the "Dirty Thirties" was literally quite what its name implied-dirty! During the period of 1930-1940, located in the heart of the Great Plains of the United States, was a series of massive dust storms and long-term drought. Another well-earned nickname this region was known for was the Dust Bowl. The Great Depression occurred at this time as well and added to the suffering placed upon the many poor farmers of the Southwest region. What could have caused one of the worst and longest droughts in recent U.S. history? Unfortunately, decades of human influence from bad farming practices, loss of soil moisture, and depletion of vegetation helped create wind-blown erosion that shaped the massive dust storms and severe droughts. Other natural causes were unusual weather patterns: warmer Atlantic and colder Pacific sea-surface temperatures, feedback mechanisms from dry air, and a strong jet stream confined to the north of a continental high pressure system that left little chance for rainfall.…

    • 2111 Words
    • 9 Pages
    Powerful Essays
  • Good Essays

    Slim Wave in Singapore

    • 512 Words
    • 3 Pages

    medicines” that are not bound by these regulations, and fail to list ingredients at all.3…

    • 512 Words
    • 3 Pages
    Good Essays
  • Powerful Essays

    Alternative Medicine Throughout recorded history, people of various cultures have relied on what Western medical practitioners today call alternative medicine. The term alternative medicine covers a broad range of healing philosophies, approaches, and therapies. It generally describes those treatments and health care practices that are outside mainstream Western health care. People use these treatments and therapies in a variety of ways. Alternative therapies used alone are often referred to as alternative; when used in combination with other alternative therapies, or in addition to conventional therapies they are referred to as complementary.…

    • 2355 Words
    • 10 Pages
    Powerful Essays