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FDA Funds Safety Monitoring and Expects Hydroquinone Monograph

The Center for Food Safety and Applied Nutrition (CFSAN) recently received US$66.8 million in funding out of the US$150 million allocated for the US Food and Drug Administration (FDA).

Prescription Polymer Nail Treatment Approved by the FDA

The U.S. Food and Drug Administration (FDA) has approved a prescription polymer treatment for brittle nail symdrome (nail dystrophy).

FDA Issues Warning Letter for Injectable Tan Product

The US Food and Drug Administration (FDA) has issued a warning letter to Melanocorp Inc. concerning the sale and marketing of the product Melanotan II.

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FDA Talks Cannabis Next Steps, Announces Public Hearing

The new steps will include the creation of an eternal agency that will explore potential pathways for the lawful marketing of products with CBD.

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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.

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FDA to Hold Public Meeting In Preparation of ICCR Meeting

Information gathered from the public meeting will help the FDA prepare for the International Cooperation on Cosmetics Regulation-12 (ICCR-12) meeting to be held July 10-12, 2018, in Tokyo, Japan.

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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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FDA Sets Regulatory Framework for Regenerative Biological Therapies

It's a sign of the times when technology and innovation hit a point where the U.S. Food and Drug Administration must stop and write new rules to ensure consumer safety. That time, with respect to regenerative biological therapies, is now.

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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.

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.

ADA Requests Tooth Whitener Classification from FDA

The American Dental Association (ADA) has published a statement requesting that the US Food and Drug Administration (FDA) establish appropriate classifications for tooth-whitening chemicals.

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 Sued Over Salon Products Containing Formaldehyde

The groups claim that the FDA has not sufficiently reacted to the concerns regarding the health risks that salon keratin hair products containing formaldehyde present.

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.

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What Dermatologists, FDA Say about Halloween Makeup

Spooky makeup fills novelty shops this time of year, but what did dermatologists and other experts have to say about safety and ingredients?

According to data from the Instituto de Comercio Exterior (ICEX), the American market is the market that imports the largest quantity of beauty products from Spain.

Mixer & Pack Receives FDA Registration Under MOCRA

Its facilities are now registered to operate in the United States.

FDA and Academia: Institutions to Collaborate Under Nanotech Initiative

Over-arching goals have spurred a collaboration to develop safe and effective nano-engineered products. While these efforts concentrate on medical use, implications for personal care are on the horizon.

The FDA has issued 15 warning letters to companies selling products containing CBD.

U.S. FDA Issues 15 Warning Letters Over CBD Products

“We remain concerned that some people wrongly think that the myriad of CBD products on the market, many of which are illegal, have been evaluated by the FDA and determined to be safe," said FDA principal deputy commissioner Amy Abernethy, M.D., Ph.D.

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