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Section: Cosmetic Ingredients

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VIDEO: 2 Questions on the FDA's Triclosan Ruling

The FDA's ruling on triclosan raises two questions, which David C. Steinberg describe in this fourth video in our series. However, he concedes that fighting the ruling is like "doubling down on an already-lost bet."

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.

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FDA Clears the Air on CBD Reform Efforts

While CBD is trending across market segments, the rules in play to ensure public health and market direction are baffling at best. As such, the FDA has issued an update outlining its efforts to provide clarity.

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Road to Regulation: Microneedling Devices Defined by FDA

Microneedling devices have, for some time, been without widely enforced regulation. As such, the U.S. Food and Drug Administration released a draft guidance on Sept. 15, 2017, defining when tools are considered esthetic vs. medical in nature, along with potential regulatory changes.

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Antibacterial Soap? You Can Skip It, Says FDA

The FDA is issuing a final rule under which OTC consumer antiseptic wash products containing the majority of the antibacterial active ingredients—including triclosan and triclocarban—will no longer be able to be marketed.

FDA Releases Draft Guidance Toward Nanotech Regulation

The US Food and Drug Administration (FDA) has released a draft guidance outlining its view on how to identify whether regulated products contain nanomaterials or apply such technologies.

FDA Clears Isoprenylcysteine Analog for Rosacea Treatment

A isoprenylcysteine (IPC) analog manufactured by biopharmaceutical company Signum Dermalogix Inc. (Dermalogix) has been approved by the U.S. Food and Drug Administration (FDA) for the treatment of rosacea.

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Chinese Hand Sanitizers Make FDA's Growing Hot List

Recent additions to the U.S. Food and Drug Administration's hand sanitizer "hot list" include several products from China, Mexico and Korea.

Comparatively Speaking: US FDA Categories of Hand Sanitizer Actives

Anthony J. O’Lenick, Jr. turns to David R. Macinga, PhD, and James W. Arbogast, PhD, to explain the differences between the US FDA categories used to classify hand sanitizer actives.

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FDA's Quarterly Color Additives Report: Red Alert

"Most notable in this certification report is the total absence of Red 6 Lake," Kelly Dobos reports.

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FDA Warns 1,500 New Sanitizer Makers: Follow the Rules

Safety and fraudulent claims are new concerns in the hand sanitizer market. Since the U.S. Food and Drug Administration (FDA) eased restrictions, some 1,500 new hand sanitizer manufacturers have registered to help; but many are not following the FDA's policy.

Frequency of Use of Organic UV Filters as Reported to the FDA

The author reports on frequency of use of 17 organic UV filters in nearly 18,000 formulations voluntarily reported to the United States government as of May 2003.

Certification must be performed before the color additive is permitted for use in products marketed to U.S. consumers.

U.S. FDA Proposes Fee Increase to Certify Color Additives

If finalized, the proposed rule will implement a 10 cent per pound increase in color certification fees.

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FDA Permits Compounding, Alcohol-based Hand Sanitizer Production

The U.S. Food and Drug Administration (FDA) has issued two guidance documents to communicate its policy for the temporary manufacture of certain alcohol-based hand sanitizer products, in response to the coronavirus (COVID-19) pandemic.

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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...

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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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.

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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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