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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.

New Black Pigment Approved By FDA

D&C Black No. 3, or "bone black," has been approved by the US Food and Drug Administration (FDA) for formulation into eye shadow, eyeliner, mascara and face powder.

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 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 Regulates Cattle Materials in Cosmetics

The US Food and Drug Administration (FDA) has published a final rule regulating the use of cattle materials in human food and cosmetics.

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FDA Updates CFSAN Education Resource Library

Designed for personal and professional use, the library covers cosmetic safety, dietary supplements, food safety, nutrition and industry information such as food defense.

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US FDA Releases Report on Color Additives

The U.S. Food and Drug Administration has released is first quarter report for 2019 on certified color additives.

The FDA does not intend to enforce the requirements related to cosmetic product facility registration and cosmetic product listing for an additional six months after the December 29, 2023, deadline.

FDA Delays MoCRA Enforcement by 6 Months

The U.S. Food and Drug Administration (FDA) announced it will delay the enforcement of facility registration and product listing requirements under MoCRA for six months after the Dec. 29, 2023, deadline to give the industry "sufficient time" to submit.

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Facing a Recall? The FDA Offers Advice

In order for a recall to be effective, timely (and as painless as possible), it’s crucial that companies be prepared to take all necessary steps once it is initiated. The U.S. FDA is drafting a guidance to help.

The FDA's 'Wish List': A Unified Agenda

The Regulatory Flexibility Act of 1980 and Executive Order 12866 require the publication of a semiannual inventory of the rulemaking under development, and the US Department of Health and Human Services (HHS) publishes this wish list for the FDA. The latest came out on Dec. 7, 2009.

The company’s colorants are sustainable with precision manufacturing practices, offering long shelf life while reducing any food or animal extracts.

RK Pigments Manufactures FDA Batch-certified Colorants

RK Pigments’ colorants are sustainable, processed using precision manufacturing practices and offer long shelf life while reducing any food or animal extracts.

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Will CBD Cosmetics Face Greater FDA Scrutiny?

As the demand for CBD products continue to grow in 2020, so will the U.S. Food and Drug Administration (FDA) crackdown on their regulation. As explained in this report, the FDA plans to continue investing in regulations for a wider spectrum of CBD-containing cosmetics and foods.

FDA Globalization Act to Effect Beauty Industry

The US House Committee on Energy and Commerce released a draft of legislation regarding provisions of adequate funding and authority for the FDA.

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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?

FDA DODAC Approves Eyelash Drug

Allergan Inc. has announced that the U.S. Food and Drug Administration DODAC voted unanimously to recommend that the FDA approve Latisse.

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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."

IBA’s Virtual FDA Cosmetics Regulations Workshop

Sep 20th, 2023Sep 21st, 2023

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FDA Issues Draft Guidance for Topical Drugs

Contact dermatitis from topical drugs and human safety are the topics in a recently issued guidance document made available by the FDA. Comments are sought through May 8, 2020.

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