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.
In Pearson v. Shalala, when appellant tried to validate the health claims as per the procedure for evaluating the validity of health claims for the dietary supplements (21 CFR section 101.7), the FDA denied to include the four health claims on the labels for the dietary supplements marketed by Mr. Pearson and Mr. Shaw11. The FDA deemed that the claims lack the significant scientific agreement standard because the evidence provided for approval includes the research that examines the relationship between consumption of foods containing the components of dietary supplements and the risk of the diseases. On that basis, the FDA determined that the specific effect of the dietary supplement components could not be determined with certainty11. Along with that, the government disputed that the appellants proposed health claims could create confusion among the consumers11. In response to this, the appellant argued that their First Amendment rights have been impaired as under Administrative Procedure Act because the FDA was required to provide
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
The Federal Trade Commission does not have adequate regulations. PART II: The Federal Trade Commission does not have adequate regulations. The FTC does not have adequate regulations regarding misleading food/drink product labels. Dietary Supplements are severely lacking in regulation and policing power.
This law was formed in order to regulate product labeling. It made sure that the food or drug label was not false or misleading. It also prevented food from having any hazardous ingredients in it, such as food or drugs being produced in dirty working conditions. In 1938, the Food, Drug, and Cosmetic Act was passed. This included “cosmetics and medical devices under control, required that drugs be labeled
Many companies and people had failed to label foods and drugs properly claiming that they are something they are not. “Before the act, companies could alternate ingredients for a more inexpensive, low quality substitute. This made for a better profit for the producers” (“Results/Impact.”). However, with the Pure Food and Drug Act these “companies could either shut down or label the foods properly” (“Results/Impact.”). Many were against consuming products that were harmful to them which is why “[t]he House vote was 240-17” (Robertson, Derek, et al.), making the Pure Food and Drug Act of 1906 “one of the most daring demonstrations of bureaucratic autonomy in the history of the United States” (“Pure Food and Drug Act (1906).”).
Food companies jump through meticulous hoops just for the reason of withholding nutritional information from their customers. “These companies fight, tooth and nail, against labeling. The fast food industry fought against giving you the calorie information. They fought against telling you if there is trans-fat in your food. The meat packing industry for years prevented country-of-origin labeling.
If the companies were honest with us customers, this wouldn’t be an issue. Thus, if labels were honest we would not have personal and health
“Advertisement doesn't carry warning labels the way tobacco do” even tobacco ads gives a warning then why not the food companies? “And I’d say the industry is vulnerable. Fast-food companies are marketing
Author of the essay “Eat Food: Food Defined” Michael Pollan, states that everything that pretends to be a food really isn’t a food. Michael persuaded me into agreeing with his argument by talking about how people shouldn’t eat anything their great grandmother wouldn’t recognize as food and avoid food products containing ingredients that are unpronounceable, lists more than five, and contains high fructose corn syrup. He opened my eyes to information I wouldn’t have thought about or researched myself. He got into depth about a type of Sara Lee bread that contains way more ingredients than needed to make the bread, including high fructose corn syrup that isn’t good for you. Marketers are doing this to sell more of their product by making it taste
The Food and Drug Administration founded in 1848 by the work of Lewis Caleb Beck, the FDA has grown in stature and responsibility to take charge of research, development, and regulation of food and drugs. Men, like Harvey Wiley, helped to oversee the administration of effective consumer protection policies, which led to the enacting of the Pure Food and Drug Act. The Pure Food and Drug Act of 1906 was the first legislation in the country that sought to regulate pharmaceuticals and food products by requiring truth-in-labeling on products, creating inspectors of the drug and food manufacturing process, and creating a list of 10 dangerous drugs that had to be labeled at all times. It ultimately came about during the
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.
What Food Inc. tries to demonstrate is the fact that despite all of our attempts to eat healthy, the industry seems determined to ensure otherwise. They hide
When the United States federal government began to intervene in the food and drug businesses, the history of early food regulation in the United States started with the 1906 Pure Food and Drug Act. This was the first of significant consumer protection laws that were enacted by the federal government in the 20th century which also led to the creation of the food and drug administration. The main purpose was to ban foreign and interstate traffic in the adulterated or the mislabeled food and drug products. It is directed by the US Bureau of chemistry to inspect products and to refer offenders to prosecutors.
The food industry is expected to grow rapidly in the future due to improving lifestyle and rapid urbanization (“Global Fast Food Market”, 2017). With this potential demand created, KHC can easily capitalize the growing foodservice industry and tailor their products to the specific demographic (Bhasin, 2018). Another strong resource KHC can utilize is focusing on nutritious products. As the foodservice industry continues to grow, KHC should further explore on expanding its product portfolio to include healthier options. Natural and organic brands, as well, as small labels buying from local farms, have become an essential part of the consumer lifestyle (Tarkan, 2015).
