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Section: Regulations > Claims/Labeling
Sun Care
Industry Debate: US FDA vs. Sunscreens
During last month’s NYSCC Suppliers' Day, several attendees expressed frustration regarding the delay of the US Food and Drug Administration’s Final Sunscreen Monograph.
Cosmetics & Toiletries
asked its
LinkedIn
members to comment. Here’s what the market had to say.
SPF/Sun
FDA Releases a Final Sunscreen Rule
After nearly a four-year wait for an action on sunscreens, the US Food and Drug Administration (FDA) has issued a Final Sunscreen Rule, which addresses the testing and labeling of OTC sunscreen products.
SPF/Sun
PCPC, CHPA Respond to FDA’s Latest Findings on Sunscreen Absorption
In response to part two of the FDA’s sunscreen ingredient maximal usage trial, published in January 2020 in JAMA, the (PCPC) and (CHPA) released a statement reassuring consumers of product safety.
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.
Claims/Labeling
FDA Releases Nanotech Report
The International Center for Technology Assessment (ICTA) has reported that the US Food and Drug Administration (FDA) will be releasing an internal task force report and recommendations on nanotechnology oversight by the end of this month.
Claims/Labeling
FDA Weighs in on Holographic Cosmetics
Holographic, iridescent and other special effect color additives have been allowed to shine in recent consumer trends. Click through for the U.S. Food and Drug Administration's take on how these additives are regulated.
Regional
FDA Begins Expediting Recall Information
The agency is increasing transparency in the product recall process.
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.
Claims/Labeling
FDA Issues New Guidances on Nanotechnology
The US Food and Drug Administration has issued two new draft guidances on the use of nanotechnology by the cosmetics and foods industries.
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.
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
FDA Petitioned to Assess Nanotech Risk
CTA and a coalition of consumer, health and environmental groups called on the FDA to address nanomaterials in consumer products.
Claims/Labeling
FDA Issues Final Guidance on Nanomaterials
On June 26, 2014, The U.S. Food and Drug Administration (FDA) issued Final Guidance for Industry: Safety of Nanomaterials in Cosmetics, a final guidance document addressing the use of nanotechnology in cosmetics.
Claims/Labeling
FDA Cracks Down on Skin Lighteners
Skin whitening products walk the line between cosmetics and drugs, and often carry dangerous side effects. Flawless Beauty's injectable whitening products were struck down by a federal judge, putting lightening products under the lens.
Claims/Labeling
FDA Discusses 'Natural' in Food, Beverage Labeling
The U.S. Food and Drug Administration is finally talking about it: the word
natural
. Will this discussion move to cosmetics, next?
Regional
FDA Releases Color Additives Q4 Report
The U.S. Food and Drug Administration (FDA) has posted to its website the fourth quarter 2020 report on color additive certifications.
Claims/Labeling
FDA Warns About Mercury in Beauty Products
Even though these products are often promoted as cosmetics, they also may be unapproved new drugs under the law, says Linda Katz, director of FDA’s Office of Cosmetics and Colors.
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