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Section: Regulations > Regional
Regional
Croda Ingredients Aligned with FDA New Proposed Regulations for Safer Sunscreens
Croda offers a range of metal oxide dispersions that have been identified as the preferred route to safe and effective UV protection.
Regional
FDA Pushes Higher Limits, New Labeling and More Data for Sunscreens
Broad spectrum sunscreens are critical for preventing skin cancer and UV damage, yet many of their essential requirements have not been updated in years. This was the driver for new sunscreen regulatory rules proposed by the FDA.
SPF/Sun
FDA Publishes Opinion on Two Sunscreen TEAs and Is Urged for More Action by PASS
The end of February was busy for the U.S. Food and Drug Administration (FDA), which published two letters on the Time and Extent Applications (TEAs) for diethylhexyl butamido triazone (Uvasorb HEB) and amiloxate (Neo Heliopan E 1000), finding insufficient scientific evidence to claim either as generally recognized as safe and effective (GRASE) and denying their addition to the OTC Sunscreen Monograph.
Regional
Sunscreen Innovation Act Passes: What Does it Mean?
The Public Access to SunScreens (PASS) Coalition applauded the U.S. Senate's passage of the Sunscreen Innovation Act (S. 2141). While the Act aims to streamline the approval process for new sunscreen actives, will it? Industry expert David Steinberg gives his take.
People
FDA Director Honored
Cosmetic Ingredient Review (CIR) director and scientific coordinator Alan Andersen, Ph.D., has been awarded with the Distinguished Alumni Award...
Regional
FDA Questioning Hydroquinone
In an August Federal Register the US Food and Drug Administration suggested that OTC skin bleaching products should require an approved new drug application.
Regional
FDA Eyes "Functional Foods"
The FDA recently announced plans for a public hearing focused on foods being marketed as "functional foods."
Regional
FDA Prepares for Y2K
Yes, here we are in year 2000. Its well-known acronym "Y2K" has been the subject of increasing conversation over the past year. It has not arrived!
Regional
FDA Increases Presence in China
The US Food and Drug Administration (FDA) is establishing a regulating presence in China to monitor exported food and cosmetics.
Regional
EU, FDA Work Toward Harmonization
The Transatlantic Economic Council (TEC) meeting made an important step forward in harmonization between the EU and the FDA.
Regional
FDA Alert on Hydroquinone
After reviewing literature on hydroquinone, the FDA announced additional studies are needed to rule out its potential carcinogenic risk.
Regional
FDA Begins Expediting Recall Information
The agency is increasing transparency in the product recall process.
Regional
FDA Releases Regulatory Science Plan
The US Food and Drug Administration (FDA) has released Strategic Plan for Regulatory Science, its initiative to modernize the tools and methods that the agency uses to evaluate whether the products it regulates are safe for consumers.
Claims/Labeling
FDA to Focus on Nanotech Trend
The FDA announced plans to focus on nanotechnology at a public meeting to be held later this year...
Claims/Labeling
FDA Hones in on Cosmetic Claims
The FDA issued five such letters since November 2014, the most recent being sent to StriVectin. Following those letters, the FDA has also issued a document that clarifies cosmetic versus drug claims for the consumer to highlight what cosmetic companies are able to say.
Regional
ICMAD Testifies at FDA Hearings
Independent Cosmetic Manufacturers and Distrubutors (ICMAD) board member Craig Weiss, president of Consumer Product Testing, testified on March 25, 2014, during recent U.S. Food and Drug Administration (FDA) hearings on modernizing over-the-counter drugs.
Regional
FDA and SDA Address Triclosan Concern
The FDA updated its Web site on Apr. 8, 2010, with its most recent information on triclosan. According to the FDA, triclosan provides a benefit to a number of personal care products, and it does not have sufficient safety evidence to recommend changing consumer use of products that contain triclosan. However, the FDA also did not have evidence that triclosan provided any additional benefit when added to antibacterial soaps and body washes.
Regional
China FDA Cracks Down on Cosmeceuticals
China's cosmetic market is likely to be rocked by policies that prohibit medical claims for cosmetic products, along with additional ingredient regulations.
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