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375 Results
Type: News
Claims/Labeling
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.
Oral Care
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.
Claims/Labeling
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.
Regional
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.
Regional
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.
Claims/Labeling
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 As such, the U.S. Food and Drug Administration released a draft guidance on Sept. 15, 2017, defining when tools are considered esthetic vs. medical in nature, along with potential regulatory changes.
Regional
Talc Results Are In: FDA Releases 6-part Report
The U.S. Food and Drug Administration released the findings from a year-long project to test talc-containing cosmetics for the presence of asbestos. Results showed 43 samples were negative while 9 were positive.
Claims/Labeling
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.
Claims/Labeling
FDA Releases Draft Guidance Toward Nanotech Regulation
The US Food and Drug Administration (FDA) has released a draft guidance outlining its view on how to identify whether regulated products contain nanomaterials or apply such technologies.
Claims/Labeling
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?
Companies
Mixer & Pack Receives FDA Registration Under MOCRA
Its facilities are now registered to operate in the United States.
Regional
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.
Regional
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.
Actives
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.
Regional
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.
Regional
FDA to Withdraw Temporary Hand Sanitizer Production Policies
"In recent months, the supply of alcohol-based hand sanitizer from traditional suppliers has increased and now, most ... are no longer having difficulty obtaining these products. Therefore, we have determined it’s appropriate to withdraw the temporary guidances..."
Regional
FDA Publishes its Draft Guidance for Cosmetic GMPs
The U.S. Food and Drug Administration (FDA) has published its Draft Guidance for Cosmetic Good Manufacturing Practices (GMPs), an update to its Cosmetic Good Manufacturing Guidelines/Inspection Checklist, mostly to include ISO 227 16:2007 as part of an effort to harmonize GMPs internationally.
Regional
FDA Warns Brazilian Blowout for Methylene Glycol Formulation
The US Food and Drug Administration (FDA) has sent a warning letter to Brazilian Blowout for its Açai Professional Smoothing Solution. The FDA finds the product to be misbranded by stating on its label that it does not contain formaldehyde and is adulterated by containing methylene glycol, a liquid form of formaldehyde.
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