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Six important of food labelling
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History and Laws behind the Federal Food and Drug Act of 1906
As one of the primary federal consumer-protection laws in existence today, The Federal Food and Drug Act of 1906 was a law that had two primary goals for food and drugs: (a) forbid harmful ingredients and additions and (b) demand labeling of ingredients to inform consumers. According to Janssen (1981), it was hoped that the enactment of this law would eliminate adulterations and poisons sometimes found in foods, sometimes in drugs and often in both. The foundation of food and drug protection came from the development of scientific methods of analysis by the Federal Bureau of Chemistry, which we know today as the Food and Drug Administration (FDA) (Janssen).
Brief History of the Legislation
The regulations of the FDA which we know today were born from a grass roots effort in the 1870’s, the Pure Food Movement. Originally, it focused on trade interests because of competition from “replacement” food products (glucose for sugar, “lard” from cottonseed oil, oleomargarine for butter, etc.) and the intolerable differences in existing state laws to which manufacturers had to comply (Janssen, 1981). As industrialization created a demand to provide the rapidly increasing localized populations with food from distant areas, a “buyer beware” era emerged. From the use of chemical preservatives and toxic colors to the development of “patent medicines” which contained opium, morphine, heroin and cocaine; all were sold without restriction and labels did not list ing...
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...regulations, I believe the FDA should take stronger enforcement action to ensure consumer protection and ultimately consumer safety.
References
Elsner, P., & Maibach, H. (2000). Cosmeceuticals: Drugs vs. Cosmetics [Electronic version]. New York: Marcel Dekker, Inc.
Janssen, W. (1981). The story of the laws behind the labels. U.S. Food and Drug Administration: Center for Food Safety and Applied Nutrition. Retrieved September 9, 2008, from
http://www.cfsan.fda.gov/~lrd/history1.html#toc
Langran, R. & Schnitzer, M. (2007). Government, Business, and the American Economy [Electronic version]. Maryland: Rowman & Littlefield Publishers, Inc.
Young, J. (1981). The long struggle for the 1906 Law. U.S. Food and Drug Administration: Center for Food Safety and Applied Nutrition. Retrieved September 9, 2008, from
http://www.foodsafety.gov/~lrd/history2.html
government set forth the Food and Drugs Act of 1906 in response which regulated and
In her book Marion Nestle examines many aspects of the food industry that call for regulation and closer examination. Nestle was a member of the Food Advisory Committee to the Food and Drug Administration (FDA) in the 1990’s and therefore helps deem herself as a credible source of information to the audience. (Nestle 2003). Yet, with her wealth of knowledge and experience she narrates from a very candid and logical perspective, but her delivery of this knowled...
“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/.
"Pure Food and Drug Act: A Muckraking Triumph." Food and Drug Act. N.p., n.d. Web. 08 Feb. 2014.
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...
No Author. "Pure food and drug act." wikipedia 23 March 2005. 4 oct. 2007 .
To begin, the Federal Food and Drug Administration does not have the power to regulate supplements like it does with drugs. Once a product is out on the market, the FDA has to prove that it is dangerous or has illegal additives before it can be removed. The FDA has targeted around seventy tainted weight loss products after learning that they had been mixed with undeclared stimulants, diuretics, and antidepressants (Trebilcock 2). The Federal Food, and Drug, Administration is responsible for ensuring that the manufacturers of foods provide safe ingredients and the correct amount of dosages for their products.
"Regulatory Information." Federal Food and Drugs Act of 1906. U.S. Food and Drug Administration, 20 May 2009. Web. 14 Apr. 2014. .
There are over a thousand ingredients that are used in cosmetics that are already proven to be safe for human use. These ingredients can be mixed and matched creating new and unique products. Many people argue that this is not suitable for the demanding market. The craving for "new" and "im...
Law, Marc. The determinants of progressive era reform: the pure food and drugs act of 1906. Cambridge, MA: National Bureau of Economic Research, 2004. Print.
In the beginning of the 1900’s, the country made dramatic changes toward progressivism in domestic issues. These changes were first made by President Theodore Roosevelt, who signed the Pure Foods and Drug Act of 1906. This bill was made, “For preventing the manufacture, sale, or transportation of adulterated or misbranded or poisonous or deleterious foods, drugs, medicines, and liquors, and for regulating traffic therein, and for other purposes.” This would help bring progressive change to many manufacturing industries that were newly developed in the late nineteenth century. These jobs were dangerous to an equal and fair way of living for the American working class and were resolved by this act.
Pomeranz, Jennifer L. "A Comprehensive Strategy To Overhaul FDA Authority For Misleading Food Labels." American Journal Of Law & Medicine 39.4 (2013): 617-647. Academic Search Complete. Web. 4 Apr. 2014.
There once was a time where words like "light" and "low-fat" on food packages that had no nutritional meaning. As a result, shoppers were often led to believe they were buying products that were more helpful than they really were. Nutrition panels on labels were also confusing and hard to read. But the Australia New Zealand Authority (ANZFA) changed all that. In March 2001 the ANZFA defined new standardized terms that appear on food labels such as "low-fat", "reduced" and "lean" to control how food manufacturers could put their facts that are relevant to most of our dietary needs. This meaning that food labeling helps consumers to make the best possible food choice.
Samuels, Jack. "History of invention and use of MSG." Truthinlabeling.com. Truth In Labeling Campaigning, 19 Feb 1999. Web. 27 Sep 2011.
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.