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What actions can the FDA take against manufacturers that produce and market unsafe cosmetics?

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Consumer safety is the number one priority for cosmetic and personal care products companies, and manufacturers are committed to upholding strict FDA regulations as required by the U.S. Food, Drug, and Cosmetic Act (FD&C Act). The law requires that every cosmetic and personal care product and its ingredients be substantiated for safety before going to market, and that they contain no prohibited ingredients. Cosmetic companies take their safety responsibility very seriously and often surpass the requirements of the law with additional consumer safety measures.

Consumers must have confidence in the products they buy and use each day. Toward that end, cosmetic and personal care products companies invest substantial resources in scientific research and safety processes to ensure the safety of their products. Companies work with and employ thousands of chemists, toxicologists, biologists, environmental scientists and other experts to evaluate the safety of cosmetic products before they go to market.

As a result, of the more than 11 billion personal care products sold each year in the United States, there are very few adverse experiences reported to the FDA in a typical year, and of those reported, most are related to rashes or allergies. Cosmetic companies' strong commitment to safety has made cosmetic and personal care products the safest product category regulated by the FDA.

Posted on Nov 22, 2010

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1 Answer

How do I use it,do I use it as a face wash?


Timi, throw it out if it does not have instructions and a label on it.
Check the attached links,instruction and guides, Good luck
"I hope this helped you out, if so let me know by pressing the helpful button. Check out some of my other posts if you need more tips and info."

http://www.fda.gov/Cosmetics/ResourcesForYou/Industry/ucm388736.htm
http://www.fda.gov/Cosmetics/ProductsIngredients/Ingredients/ucm388821.htm
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Does the FDA check dietary supplements before they are sold?


The FDA does not check dietary supplements. It is up to the supplement's manufacturer to make sure their product is safe and that the list of ingredients on the label matches the ingredients found in the product.

According to the FDA's website: "Generally, manufacturers do not need to register their products with FDA nor get FDA approval before producing or selling dietary supplements.* Manufacturers must make sure that product label information is truthful and not misleading. Under the FDA Final Rule 21 CFR 111, all domestic and foreign companies that manufacture, package, label or hold dietary supplement, including those involved with testing, quality control, and dietary supplement distribution in the U.S., must comply with the Dietary Supplement Current Good Manufacturing Practices (cGMPS) for quality control."

Also, if you notice, supplements always contain the following sentence below the nutrition facts and other information after the nutrition facts: "These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease."

Feb 04, 2013 | Health & Beauty

1 Answer

Does maybelline use lead in their product???


Maybelline is owned by L'Oreal.And yes they do use lead . Cosmetics are not subject to pre-market approval by FDA. However, pre-market approval is required for the color additives used in cosmetics (including those in lipsticks) and other FDA-regulated products (with the exception of coal-tar hair dyes). To learn more on this subject, please refer to FDA Authority Over Cosmetics1.

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1 Answer

What voluntary steps are cosmetic manufacturers taking to provide cosmetic safety and protect consumers?


Consumer safety is the number one priority for cosmetic and personal care products companies, and manufacturers are committed to upholding strict FDA regulations as required by the U.S. Food, Drug, and Cosmetic Act (FD&C Act). The law requires that every cosmetic and personal care product and its ingredients be substantiated for safety before going to market, and that they contain no prohibited ingredients. Cosmetic companies take their safety responsibility very seriously and often surpass the requirements of the law with additional consumer safety measures.

Consumers must have confidence in the products they buy and use each day. Toward that end, cosmetic and personal care products companies invest substantial resources in scientific research and safety processes to ensure the safety of their products. Companies work with and employ thousands of chemists, toxicologists, biologists, environmental scientists and other experts to evaluate the safety of cosmetic products before they go to market.

As a result, of the more than 11 billion personal care products sold each year in the United States, there are very few adverse experiences reported to the FDA in a typical year, and of those reported, most are related to rashes or allergies. Cosmetic companies' strong commitment to safety has made cosmetic and personal care products the safest product category regulated by the FDA.

Nov 22, 2010 | Health & Beauty

1 Answer

Is the safety of a cosmetic product evaluated once it hits the market?


Cosmetic safety reassurance does not end once a product is placed in the marketplace. Companies engage in ongoing, active monitoring of consumer experience to confirm cosmetic product safety.

Cosmetic and personal care product manufacturers have established post-market surveillance processes for the identification of potential safety issues related to their products. Such systems help to identify consumer use patterns, such as alternate uses or product combinations that may contribute to adverse events. These processes include regular surveys of consumer contacts received by a marketer or manufacturer either through toll-free 1-800 numbers on packages or direct correspondence.

Trend analyses of contact data, including evaluations of frequency and severity of adverse events, as well as comparison of these trends with historical information for other comparable products, also represent valuable mechanisms for identification of safety-related concerns. Although adverse reactions that are both serious and unexpected are extremely rare for cosmetic and personal care products, manufacturers must report knowledge of any instances of serious product reactions to the U.S. Food and Drug Administration.

Nov 22, 2010 | Health & Beauty

2 Answers

Doesn’t the government certify that personal care products are safe and healthy before they can be sold to consumers?


No. Major loopholes in federal law allow the $50 billion cosmetics industry to put unlimited amounts of chemicals into personal care products with no required testing, no required monitoring of health effects, and inadequate labeling requirements.

Neither cosmetic products nor cosmetic ingredients are reviewed or approved by the Food and Drug Administration (FDA) before they are sold to the public. FDA cannot require companies to do safety testing of their cosmetic products before marketing

Nov 22, 2010 | Health & Beauty

1 Answer

How are the FDA and cosmetics manufacturers working together to ensure consumer safety?


Consumer safety is the number one priority for cosmetic and personal care products companies, and manufacturers are committed to upholding strict FDA regulations as required by the U.S. Food, Drug, and Cosmetic Act (FD&C Act). The law requires that every cosmetic and personal care product and its ingredients be substantiated for safety before going to market, and that they contain no prohibited ingredients. Cosmetic companies take their safety responsibility very seriously and often surpass the requirements of the law with additional consumer safety measures.

Consumers must have confidence in the products they buy and use each day. Toward that end, cosmetic and personal care products companies invest substantial resources in scientific research and safety processes to ensure the safety of their products. Companies work with and employ thousands of chemists, toxicologists, biologists, environmental scientists and other experts to evaluate the safety of cosmetic products before they go to market.
As a result, of the more than 11 billion personal care products sold each year in the United States, there are very few adverse experiences reported to the FDA in a typical year, and of those reported, most are related to rashes or allergies. Cosmetic companies' strong commitment to safety has made cosmetic and personal care products the safest product category regulated by the FDA.

Nov 22, 2010 | Health & Beauty

1 Answer

Who regulates cosmetics in the U.S. and under what laws?


The marketing of cosmetics in the U.S. is regulated by the Office of Cosmetics and Colors within the
Food and Drug Administration (FDA) Center for Food Safety and Applied Nutrition pursuant to the
Federal Food, Drug, and Cosmetic Act (FFDCA)2 and the Fair Packaging and Labeling Act.

Nov 22, 2010 | Health & Beauty

1 Answer

Does FDA specifically require that cosmetics or their ingredients be tested on animals?


No. In contrast to most other products regulated by FDA, cosmetics and their ingredients are not subject to specific testing requirements or pre-market approval by the agency. However, the FFDCA broadly prohibits the marketing of "adulterated" or "misbranded" cosmetics, including any product
(other than a hair dye) that "bears or contains any poisonous or deleterious substance which may render it injurious to users...."4-5 In other words, cosmetic manufacturers are responsible for assuring the safety of their products and the ingredients they use, but are not required to use animal tests to do so.

Nov 22, 2010 | Health & Beauty

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