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Non-acetone Nail Polish Remover

FDA Recalls Nail Polish Remover After Burn Reports

The US Food and Drug Administration (FDA) has issued a statement recalling of Non-Acetone Nail Polish Remover due to a possible health risk.

Advocacy Groups File Suit Against the FDA Over Nanotechnology Regulation

A coalition of six consumer safety and environmental groups is suing the US Food and Drug Administration (FDA) over its lack of nanotechnology regulation, specifically for sunscreen.

While the overall trend for color cosmetics has been positive, a return to pre-pandemic levels appears to be progressing slowly.

Lipstick Forecasts Not So Rosy, FDA Color Additives Report Reveals

Many trend agencies and news outlets are reporting an increase in lipstick sales for 2022 but those numbers may not paint the full picture. Here's what the latest FDA Color Additives report reveals, as outlined by industry expert Kelly Dobos.

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FDA Proposes Labeling Rule for Color Additives [Feb. 2, 2006]

The U.S. Food and Drug Administration (FDA) published a proposed rule in the Federal Register requiring the declaration of carmine and cochineal extract...

FDA Cracks Down on Medicinal Claims Regarding Bee By-products

The US Food and Drug Administration (FDA) cracked down on Wisconsin-based Beehive Botanicals Inc. after the company did not comply with requests to remove and change misbranded and unapproved claims from its Web site and labels.

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6 Sanitizer Offenses, Color Additives and Cosmetic Registrations: FDA Update

The U.S. Food and Drug Administration recently issued updates regarding color additives certification, voluntary cosmetic registrations and hand sanitizer violations.

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Nature Essence Small Molecule Co. Pinged by FDA Warning Letter

In addition to several food and beverage violations, the U.S. FDA cited adulterated cosmetics and new drug claims in its warning letter to the company.

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[update] US FDA Orders Lead Ingredient Out of Hair Color

The final ruling is a response to a color additive petition over safety concerns of lead acetate, which allows for gradual color change in "progressive" hair dyes.

In response to the FDA's proposed ten cent per pound fee increase, Dobos explains how the price has not been adjusted since 2005 and represents an approximately 30% increase.

Dobos Responds to U.S. FDA's Proposed Color Additive Fee Increase

Considering the U.S. Food and Drug Administration's (FDA's) proposed ten cent per pound fee increase on color additives, Dobos responds here noting that the price has not changed since 2005 but it also represents an approximately 30% increase.

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ACI, CHPA Urge FDA: Withdraw Allowance for Emergency Sanitizer Production

Citing public safety concerns, the American Cleaning Institute (ACI) and Consumer Healthcare Products Association (CHPA) are urging the U.S. Food and Drug Administration (FDA) to withdraw its temporary guidance allowing non-traditional manufacturers to produce hand sanitizers.

The U.S. Hemp Roundtable said the FDA’s comments signal 'the new year may offer some promise for the long-awaited regulation of hemp-derived extracts such as CBD.'

FDA to Explore CBD, Hemp Regulations for Food and Supplements

The U.S. Food and Drug Administration (FDA) is exploring whether legal cannabis is safe in food or supplements and expects to make recommendations in the coming months for regulating such products. Could this translate to cosmetics?

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FDA Issues More Sanitizer Warnings, Posts Microbe-related Recalls

Sanitizer warning letters and "hotlist" additions, plus microbe-related recalls are among the latest cosmetic-relevant updates from the U.S. Food and Drug Administration.

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U.S. FDA Red Flags Careful Cents, LLC for COVID-19 Claims

Careful Cents, LLC, is marketing essential oils that, according to the U.S. FDA, are misbranded drugs based on their claims. The agency issued a warning letter highlighting examples including immunity-boosting and antiviral effects, and positioned to address COVID-19.

L'Oréal Receives A Warning Letter From the FDA for Drug Claims

The US Food and Drug Administration (FDA) has issued a warning letter to L'Oréal for gene, stem cell and skin regeneration claims associated with Lancôme products.

ACI and PCPC Form Coalition to Promote Antibacterial Use to the FDA

The Personal Care Products Council (PCPC) and the American Cleaning Institute (ACI), which have formed the Topical Antimicrobial Coalition, have submitted their comments to the U.S. Food and Drug Administration (FDA) regarding its proposed rule, which they find could elliminate access to antibacterial soaps and increase foodborne illness.

FDA Commissions Study of its Drug, Biologics Application Processes

The U.S. Food and Drug Administration (FDA) released a new report that examines the way the agency reviews applications for drugs and biologics that have not previously been approved by the FDA.

Sindoor Powder Under FDA Fire for High Lead Content

The US Food and Drug Administration is warning consumers to avoid the use of sindoor powder marketed under the Swad brand due to its high lead content.

FDA Rule for Broad-spectrum Labeling: Key Substrate Findings

UVA protection is part of the mandatory testing for claiming broad-spectrum sun protection. A worldwide standardization is in development with the ISO TC217, expected for UVA testing 2012. The FDA has issued a final rule following Colipa’s proposed UVA in vitro method. While this rule establishes UVA labeling and testing, inconsistencies remain. This study compares the critical wavelength in roughness and application before and after two levels of UV doses.

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