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Type: News

Section: Regulations > Claims/Labeling

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.

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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.

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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.

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FDA Begins Expediting Recall Information

The agency is increasing transparency in the product recall process.

FDA to Focus on Nanotech Trend

The FDA announced plans to focus on nanotechnology at a public meeting to be held later this year...

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.

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.

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.

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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.

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.

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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.

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.

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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?

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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.

FDA Issues Warnings for Cosmetics, Website Claims

The FDA has taken recent compliance actions by issuing warning letters for cosmetics claims and unapproved ingredients.

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.

FDA Issues Warning Over Hand Sanitizer Claims

The US Food and Drug Administration (FDA) has issued a warning letter to Procter & Gamble Co. over hand sanitizer claims.

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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.

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