Wait a second!
More handpicked essays just for you.
More handpicked essays just for you.
Importance of nutrition in human
Importance of nutrition in human
Importance of nutrition in human
Don’t take our word for it - see why 10 million students trust us with their essay needs.
Recommended: Importance of nutrition in human
When we go to the store and buy our groceries, we expect the labels we read to be accurate. Many people rely on labels to help them stay safe and healthy. However there have been incidents where this is not the case. It has been found that in certain foods there are unlisted ingredients added to foods that claim they are “100% juice”, these unlisted ingredients are unfair to consumers who expect their labels to be accurate. Labels and packaging have also been found to be misleading. For the consumer who is trying to diet and is looking for a healthier option, the packaging can be confusing and untruthful. The naturalness of a product is also questionable because of all the added pesticides. All of these factors have led to serious issues …show more content…
Many new laws have come from this, now products are required to have the country of origin as well. Originally foods and drugs were not required to have labels. It has come a long way, reaching many milestones, beginning in 1820 with eleven chemists meeting “to establish the U.S. Pharmacopeia, the first compendium of standard drugs for the United States. In 1912 Congress enacted the Sherley Amendment to overcome the ruling in U.S. v. Johnson. It prohibits labeling medicines with false therapeutic claims intended to defraud the purchaser (FDA)”. In 1937 Elixir of Sulfanilamide which contained the poisonous solvent diethylene glycol, killed 107 people, mostly children. This enforced “the need to establish drug safety before marketing and to enact the pending food and drug law (FDA)”. In 1938 congress passed the Food, Drug, and Cosmetic Act. This created new regulations for the food, drug and cosmetic industries (US FDA). Without these and many other acts, food labeling would not be where it is today, however there is still much needed improvement.
The first reason is how the inaccuracy of food labeling can have adverse consequences involving an individual with a food allergy. Individuals with a food allergy commonly check the ingredients listed in their items before consuming, however if their allergen is not listed it could result in an allergic reaction or even death. It has been found that as many as one-fourth of all food manufacturers do not list their raw ingredients such as nuts or eggs, common foods that many are allergic to (FDA
Adverts often mask foods that are unhealthy by emphasising its positive nutritional features – such as dietary fibre and protein. While at the same time ignoring its negative features – including the high amounts of saturated fat and sugar contents. In some cases, even products that mention any alleged health benefits are usually are outweighed by the health risks associated with consuming the product, that they just fail to
government set forth the Food and Drugs Act of 1906 in response which regulated and
“Pure Food and Drug Act 1906.” 34 U.S. Stats. 768, quoted in Medicine in the Americas, Bethesda, Maryland: National Library of Medicine, 2004. http://www.ncbi.nlm.nih.gov/books/NBK22116/.
A recent study in 2015 reports that over 15 million people in America have food allergies that is 1 in every 13 people under the age of 18. Making it very likely that somebody in this room is part of these 15 million American’s who have food allergies. If you are somebody who has food allergies, or you know of someone who has food allergies, this speech will help you better understand more about food allergies, so you can deal with food allergies and more importantly be more careful around other people who do. So today, I am going to be informing you about Food allergies.
The momentum generated by the passage of the Meat Inspection Act helped secure the passage of the Pure Food and Drug Act, which had been stalled in Congress since 1905. With these two pieces of legislation, the federal government took important steps to assure the public that the food they were eating met minimu...
was designed to avoid mislabeled food and drug products and was the start of making sure every
"Regulatory Information." Federal Food and Drugs Act of 1906. U.S. Food and Drug Administration, 20 May 2009. Web. 14 Apr. 2014. .
...ous tests (Law, 2004). They also must now have the FDA’s approval in order for a certain food or drug to be sold directly to consumers. Also the marketplace has changed, due to new ways to process the product in a more safe and effective manner. There were also changes due to political, economical, social, and cultural changes since 1906. In conclusion, the Food and Drug Act paved the way for the Progressive movement and food safety in America.
Companies nowadays are using different and strong methods in marketing their food products. The Companies are very competitive, and the results can affect the people. When we think about this job field, it is convincing that those producers should use cleverly ways to gain their own living. In the other side they shouldn’t use misleading ways that could harm the people. Food companies should be straightforward with every marketing method they use. People have the right to know what they are consuming and also to know the effects of these products on them, whether it is harmful, useful, or even neutral.
The Federal Drug and Food Administration, or FDA, began in 1906 as part of the Pure Food and Drug Act. The 1906 Act was passed due to a culmination of bills passed that were focused on severe abuses in the consumer market. Laws and guidelines were created by the FDA to monitor food safety. Product manufacturing facilities are inspected to show they are in compliance with these laws and guidelines. The FDA does not, however, test to see if food is safe for human consumption. The manufacturers are responsible for testing food, and then give their results to the FDA for inspection. Unfortunately testing done on food today does not show us the long term effect of new additives and chemical compound. It may take several years for a new chemical or additive to cause side effects...
In Lee Ann Fisher Baron’s “Junk Science,” she claims that the “food industry with the help of federal regulators” sometimes use “[a science that] bypasses [the] system of peer review. Presented directly to the public by…‘experts’ or ‘activists,’ often with little or no supporting evidence, this ‘junk science’ undermines the ability…[for] everyday consumers to make rational decisions” (921). Yet Americans still have a lot of faith in the U.S. Food and Drug Administration (FDA). According to a 2013 Pew Research study, 65% of Americans are “very favorable” or “mostly favorable” of the FDA. When it comes to what people put in their bodies, the FDA has a moral obligation to be truthful and transparent. The bottom line of the FDA’s myriad of responsibilities is to help protect the health of Americans. Deciding what to eat is a critical part of living healthily, and consumers must be able to trust that this massive government agency is informing them properly of the contents of food. While the FDA does an excellent job in many areas, it has flaws in other areas. One of its flaws is allowing the food industry to print food labels that are deceptive, unclear, or simply not true (known as misbranding). This is quite the hot topic because a Google search for “Should I trust food labels” returns well over 20 million results, many of which are blog posts from online writers begging their readers not to trust food labels. HowStuffWorks, a division of Discovery Communications, published an online article whose author claims that “[the food industry] will put what they want on labels. They know the game….” While the food industry is partially at blame for misbranding, the FDA is allowing it to happen. If a mother tells her children that it is oka...
Too much information on a food label might have caused a lot of painful headaches for consumers, but it's all worth it, due to many health and nutrition problems. By law, manufacturers must abide by the standard code terms of what is put on their food label. By this, a food label must have no false claims or information, be in English, legible and easy to see. Also must contain a barcode, name of food, list of ingredients in descending order of weight, net weight, any additives in the food, country of origin, use of imported ingredients, name and address of manufacturer, date marking and nutrition panel if any claims are made. Food and Health claims Food claims seemed to be marketing to a manufacturer, but now it is a warning to a consumer's health.
Hank Cardello, a former food executive, expresses the idea that grocers and other food executives do not have your best interest in mind in “What Grocers Don’t Want You to Know.” Cardello states that grocers set up supermarkets “like taking a choreographed tour through Disney World”(30). Getting to all of the products you want is easier than ever, but getting what you need has proven more difficult. During my own field research, I had discovered that getting the bare necessities (i.e. milk or even bread) were the hardest items to find in the supermarket I visited. It was even harder to find the truly organic form of these products. Why is it so hard to find something healthy in the food market? This is due to the subsidizing of these large food companies and them teaming with grocers to sell their products. Although it is hard to find these natural products, it is possible. Larger food companies use a lot of things to keep their items on the shelf. Preservatives are commonly found in these unhealthy products. Vileisis states in another chapter “Rise of the Modern Food Sensibility” that throughout history these preservatives have proven to be harmful. In one study she covers Harvey Wiley, a member of the U.S. Bureau of Chemistry, discovers that in 1904 that many preservatives, are harmful to our kidneys and livers (126-28). This can cause many
Wallace F. Jansseen, an FDA historian, in his article “The Story of the Laws Behind the Labels” writes about the initiation of the agencies that later developed into the FDA. Jansseen points out that the earliest forms of the FDA started out as the Department of Agriculture in 1862. Charles M. Wetherill was the first chemist that as a part of the Department of Agriculture. His main purpose was to test food, fertilizers, soils, and other agricultural substances. At first his experiments revolved around agricultural research but inevitably became involved in food safety to find adulterated substances. Jansseen points out that many of the substances that were tested were counterfeit, contaminated, diluted, and decomposed drugs. Eventually his practice of finding adulterated substances was noticed in 1906 as part of the Food and Drugs Act.
More and More people are becoming concerned about what they eat, especially if they consume food products that are manufactured in food industries. However, it is hard to know what exactly you are consuming if food industries provide false nutrition content and mislead consumers by placing false advertisements on the packaging. When a company produces a product that contains misleading label, consumers are not receiving complete information about the food they are eating which could lead to health issues including allergies and problems with diabetes.