ipl-logo

Supplement Labeling Essay

1720 Words7 Pages

Introduction The necessity of supplement labeling is a heavily debated topic in the United States (US). Regulation of supplements in the United States falls on the Food and Drug Administration (FDA). There is a norm of less stringent regulation that makes it difficult for policy to change. This norm may benefit one actor, like the producer, at the expense of the consumer. Safety becomes the number one priority for the regulator, but they are limited to acting only when harm is apparent and undeniable. There are several individual and institutional factors that influence how supplement labeling has changed and will be regulated in the future. Background Legislation on supplement labeling has undergone a few drastic changes over the years. In 1938, the Federal Food, Drug and Cosmetic Act (FFDCA) differentiated between a drug and a supplement. A supplement is different that a drug because it is not intended to cure a disease. The FFDCA gave the FDA authority to regulate supplements. The main priority of the FDA is to …show more content…

It defined dietary supplements as “ a product intended to supplement the diet that contains one or more of the following: a vitamin, mineral, an herb or other botanical, an amino acid.”. Under this act, supplement producers cannot misbrand, use false or misleading labels, or adulterate, add impure substances that may cause illness, their products. There does not need to be scientific supports as long as it adheres to the two previous rules. It is important to that note that while, the FDA is principle regulator of supplements and their ingredients, regulation also falls under the presidential and congressional oversight. The regulatory power of the FDA has expanded over the years with DSHEA being the current framework for supplement

Show More
Related

Why Is It Unethical To Target Uniformed Consumers

271 Words | 2 Pages

Consumers barley read whats in the stuff they are taking in. Not to add, they can not know what they're taking in if it is never writing on the bottle. It is unethical to target these consumers. It could hurt the consumer causing a lawsuit or furthermore shutting down the company. FDA should regulate this kind of stuff so it never happens.

Read More

Summary Of Stories That Changed America By Carl Jensen

1184 Words | 5 Pages

This eventually led to the creation of the federal department of Food and Drug Administration which lays out laws for what is safe for inclusion in the food and medicine consumed by the

Read More

Impact Of Upton Sinclair's The Jungle On The Meat Factories During The Progressive Age

1317 Words | 6 Pages

Although there had to have been an obligation before to pass the Pure Food and Drug Act. Professor Harvey Washington Wiley wanted to take action and stop the production of the misinterpretation of real medicine. He lead a campaign wanting to end this dilemma, by using propaganda and research he wanted to influence others to take action and react to the lies that were being filled and distributed in bottles of medicine. Even though Wiley presented all of his information, Sinclairs profounding novel was what finally brought the Food and Drug Act to a realization. The Pure Food and Drug Act was a law set up to stop the marketing of ambiguous medicine or medicine that was deteriorated, became hazardous to the people.

Read More

Dr Pepper Case

876 Words | 4 Pages

Perhaps the prominent regulation that most everyone is familiar with, is the listing of required nutritional facts about what the product contains. Just navigating the regulations in this environment is often not enough though, companies should be proactive in dealing with possible changes, potentially staving them off in the long run, which is part of the reason that Dr Pepper undertakes so many healthy living initiatives, along with Coke and Pepsi, to encourage consumers to make better decisions, and maybe buy diet product, rather than the company have to comply with the costs of reconfiguring its labels, in a manner that was proposed by the FDA in 2014, which would have required actual column nutritional facts label. In part due to the soda companies efforts, this initiative seems to have lost initiative for the time being. This is likely due to the fact that Dr Pepper does not operate, for the most part, beyond the United

Read More

Summary Of The Jungle By Upton Sinclair

1165 Words | 5 Pages

Roosevelt’s plea lead to the creation of the Meat Inspection Act, which allowed the U.S. Department of Agriculture to inspect meat and decide whether or not it was suitable for consumption. While Dr. Wiley and his team were happy to finally see a change, they weren’t satisfied with the amount of change. That further led to the creation of the Pure Food and Drug Act, which was signed into law on June 30th, 1906, at the same time as the Meat Inspection Act. The Pure Food and Drug Act finally called for proper labeling of drugs and food and banned misleading labels, and some dangerous additives. The Bureau of Chemistry was tasked with enforcing the laws of the Pure Food and Drug act, until 1927 when it became the

Read More

Summary Of The Jungle By Upton Sinclair

997 Words | 4 Pages

The FDA is a government agency that had the responsibility to protect the health of the nation from impure and unsafe drugs, food, cosmetics, and other products. The FDA did this by administering the regulation of biological products shipped within the United states and with foreign countries. The FDA must approve all drugs before they can be sold in the United States. It also inspects manufacturing facilities and it tests the products to be sold to make sure they meet the current standards and it

Read More

Upton Sinclair The Jungle Sparknotes

1569 Words | 7 Pages

The publication fueled the enactment of the Pure Food and Drug Act of

Read More

Upton Sinclair's Impact On The Jungle

904 Words | 4 Pages

Not only had the act progressed food safety, it had also made one of the most well known organizations to this date, the FDA. With this accomplishment, The Jungle had reached a height unthinkable—it had influenced the political climate of the Progressive

Read More

What Are The Problems That Muckrakers Faced During The Progressive Era

1120 Words | 5 Pages

The Pure Food and Drug Act made it illegal to sell mislabeled or contaminated food. The Meat Inspection Act made it illegal to sell altered or misbranded meat and that it was processed in clean/safe conditions. The last fix put in place was the FDA. The FDA is still up and running today. It stands for “Food and Drug Administration” and they search and test all the food we eat.

Read More

How Did The Pure Food And Drug Act 1906

562 Words | 3 Pages

Besides improving regulation and stopping mislabeling, the Pure Food and Drug Act “gave unprecedented new regulatory powers to the federal government, … [and] empowered a bureau that evolved into today's Food and Drug Administration (FDA)” (“Pure Food and Drug Act (1906).”) by creating an “economic legacy … [which] includes strong consumer

Read More

Pure Food And Drug Act Of 1906

376 Words | 2 Pages

Pure Food and Drug Act of 1906 The main purpose of the Food and Drug Act of 1906 was to ban foreign and intersate traffic in aldutered or mislabeled food and drug products, and it directed the U.S. Bureau of Chemistry to inspect products and refer offenders to prosecutors. It required that active ingredients bve be placed on the label of a drugs packaging and that drugs could not fall below purity levels established by the United States Pharmacopeia or the National Formulary. In 1906 the Pure Food and Drug Act paved the way for the eventual creation of the FDA. Upton Sinclair wrote a book titled The Jungle to expose the appalling working conditions in the meat packing industry.

Read More

Food And Drug Act Of 1906 Essay

633 Words | 3 Pages

Ever since the 1900s the Federal Government has had several growths of expansion, some good and some bad, in this article the Pure Food and Drug Act of 1906 as well as the Meat Inspection Act of 1906 will be discussed and how it expanded government, and whether this growth of government was beneficial or not. The Pure Food and Drug Act of 1906, which can be labeled as the founding date of the Food and Drug Administration (FDA) had the purpose to essentially “ban foreign and interstate traffic in adulterated or mislabeled food and drug products… (and) It required that active ingredients be placed on the label of a drug’s packaging and that drugs could not fall below purity levels established by the United States Pharmacopeia or the National Formulary” [1]. This meant that food and drug products couldn’t be lined with “mysterious” substances and everything had to be labelled according to what it contained.

Read More

Pure Food And Drug Act Of 1906 Essay

561 Words | 3 Pages

The Pure Food and Drug act of 1906 was the 1st consumer protection law by the Federal Government, this act was passed by President Theodore Roosevelt. The main purpose of the Pure Food and Drug act was to prohibit transportation of contaminated, poisonous, and misbranded foods, drugs, medicines and liquors. Without the pure food and drug act our food, medication, and other product would be filled with dangerous chemicals that would have harm in our health and potentially cause death. Before the 20th century, there were no laws or regulations that protected Americans from hazardous foods and medicines. This meant that there were no restrictions of what chemicals could be put in one’s food or medicine, leaving the open to mass deaths of contaminated or poisonous products.

Read More

Food And Drug Act 1906

1202 Words | 5 Pages

Some drug products must be proven safe before companies put them out in stores for buyers, because of the Pure Food and Drug Act regulations. The FDA must approve food additives before it used in food since additives are used to induce cancer in humans and animals. The FDA has a huge impact on keeping American intact without being harmed from dangerous and hazardous chemicals. Since the beginning of civilizations people have been concerned about the quality and safety of foods and medicine. The FDA has answered the concerns and worries for the American people.

Read More

Barbara Dunlop Analysis

989 Words | 4 Pages

Barbara Dunlop is a USA Today and New York Times bestselling author that has written over fifty novels in the romance genre. Barbara wrote her first work of fiction when she was only eight years. Her first work was titled How The Giraffe Got His Long Neck and was published to critical acclaim. Unfortunately, she had difficulties with distribution but the good reception whet her appetite for even more achievements. She would later become a reporter for The Berry Street Times a venerated publication that allowed Barbara to expand her reach.

Read More

More about Supplement Labeling Essay

Related Topics

Open Document