ipl-logo

The Importance Of Cosmetic Regulation

809 Words4 Pages

Cosmetic regulation is a misnomer. The FDA (Food, Drug, and Cosmetic Act) was created in 1938 and is the designated government agency that should control the Cosmetic Industry as well as the Food and Drug Industries. However, although it does a fair job in food and drugs, it virtually has turned its back on cosmetics and allows it to govern itself. Cosmetics have a very rich history and from the time of the Egyptians to current day the obsession for fair, beautiful skin has helped this industry to grow and prosper to over 50 billion dollars annually. The Cosmetic Industry, in all countries, is controlled by government bodies and agencies. These agencies presumably are in place for the purpose of keeping a tab on the quality of cosmetic products that are being produced. Cosmetic regulation of personal care products that are produced is the primary responsibility of these bodies. Therefore, in theory at best, US cosmetic regulations for personal care products rests with the FDA. The question becomes is the FDA truly regulating or governing the Cosmetic Industry?. The regulations framed under the FDA are quite similar to other countries but there are certain unique features. Though one of the FDA 's functions is to regulate the Cosmetic Industry, it gives more emphasis on the regulation of food and drugs. For drugs that are manufactured in the US, prior to their release into the market, they will require the necessary certification from the FDA. However, because personal

Show More
Related

  • 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

  • Meat Labeling Industry In Upton Sinclair's The Jungle

    1028 Words  | 5 Pages

    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

    Read More

  • False Claim Act Essay

    3132 Words  | 13 Pages

    OFF-LABEL PROMOTION UNDER FALSE CLAIM ACT Pharmaceutical industry plays a vital role in public health. These companies develop, manufacture and market medicines. Considering public health safety, government laid down laws and their agencies established regulations to market these medicines. Companies need to justify through clinical trials that their products are beneficial to consumers. To release a product in United States, they have to file a New Drug Application (NDA) with Food and Drug Administration (FDA) and should gain approval of the product.

    Read More

  • Argumentative Essay About The Fda

    732 Words  | 3 Pages

    The Food and Drug Administration is the oldest “consumer protection agency in the federal government”. The purpose of the FDA is to protect consumers by assuring that all food supplies,medical devices,cosmetics,human and veterinary drugs,and products that emit radiation are safe and secure for our use. Although the official label for the FDA was not created until the 1930’s it’s beginnings can date all the way back to the year of 1848. It all started with a man named Lewis Beck.

    Read More

  • Upton Sinclair's The Jungle And The Meatpacking Industry

    601 Words  | 3 Pages

    That same day, The Pure Food and Drug Act of 1906 was created. This act required the makers of prepared food and medicine to host government inspection as well. Overall, these acts have now been a reassurance to the public that meat and other things are in good

    Read More

  • Consumer Protection Act Of 1906 Essay

    720 Words  | 3 Pages

    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.

    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

  • 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

  • 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

  • Dermal Filler Marketing Strategy

    714 Words  | 3 Pages

    Dermal fillers clinics engage with a Computer marketing Company Nobody imagined technology would be incorporated in the business world and slowly replace the traditional set platform. Digital marketing strategies are the future of the marketing sector. Business owners are desperate to stand out from their competitors. The dental industry is crowded with numerous clinics. As a result, dermal fillers clinic owners should go an extra mile if they would like their brands to stand out.

    Read More

  • Animal Testing In The Cosmetics Industry: A Case Study

    1142 Words  | 5 Pages

    Part A Unethical action is an action that falls outside of what is considered morally right or proper for an individual, group or an industry. Animal testing, which also known as animal experiment. It was an action that was cruel to the animal, forcing the animals to undergo something that causes pain and suffer. (Crueltyfreeinternational.org, 2018) Meanwhile in the beauty and cosmetics industry, testing cosmetic using animal was a common process to go by.

    Read More

  • Makeup Advertising Analysis

    753 Words  | 4 Pages

    In many peoples’ lives makeup is step in their daily routine. Many people use makeup to boost their confidence and enhance their natural beauty. However, many makeup advertisements place an emphasis on people looking their best in order to sell products, which isn’t necessarily bad. Covergirl and Revlon are two makeup brands that use many tactics to appeal to consumers

    Read More

  • Pepsico Political Factors

    724 Words  | 3 Pages

    Being one of the largest non-alcoholic beverage and food industry, PepsiCo needs to be strictly regulated by Food Standards Agencies such as the European Food Safety Authority and Health, the American Medical Association, the World Health Organization and the US Food and Drug Administration (FDA). This agencies are body responsible for protecting and promoting public health through

    Read More

  • Loreal Pestel Analysis

    1016 Words  | 5 Pages

    . STUDY OF ENVIRONMENTAL FACTORS a. PEST Analysis: i. Political: L 'Oreal faced issues in the dermatology branch led by Galderma due to new legislations governing drugs. The EU law affects L 'Oreal and restricts their use of certain kinds of carcinogenic chemicals, such as Phthalates. L 'Oreal is obligated to produce safe products that do not contain any harmful substances.

    Read More

  • External Factors In The Hospitality Industry

    1245 Words  | 5 Pages

    Every industry to include the hospitality industry is impacted by external factors which directly influence organizational behavior and decision making. There are numerous factors to be considered, but political, economic, and social are three of the most influential. These outside factors sway managerial operational decisions daily regarding personnel, spending, policy, and short-term and long-term strategic planning concerning both core and exterior operations. As within every industry, the hospitality industry has unmanageable elements that affect management or ownership of hospitality establishments (Lewis 2017). Understanding these factors is important because it provides an opportunity for contingency planning (Lewis, 2017).

    Read More

More about The Importance Of Cosmetic Regulation

Open Document