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180 Results
Section: Cosmetic Ingredients
Companies
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.
Regional
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."
Tech Transfer
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.
Regional
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 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.
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 As such, the U.S. Food and Drug Administration released a draft guidance on Sept. 15, 2017, defining when tools are considered esthetic vs. medical in nature, along with potential regulatory changes.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
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.
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FDA Releases Draft Guidance Toward Nanotech Regulation
The US Food and Drug Administration (FDA) has released a draft guidance outlining its view on how to identify whether regulated products contain nanomaterials or apply such technologies.
Regional
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.
Regional
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.
Regional
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.
Regional
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.
Regional
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?
Actives
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.
Regional
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.
Claims/Labeling
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...
Regional
FDA Warns Consumers About Side Effects from Topical Acne Actives
The U.S. Food and Drug Administration has issued a warning to consumers that over-the-counter (OTC) acne products containing benzoyl peroxide and salicylic acid can cause severe irritation or severe allergic reactions in rare instances.
Actives
FDA Flags 13 More Sanitizers, Issues One Warning for Methanol Content
Methanol content or possible associations therewith account for 12 of the 13 latest additions by the U.S. Food and Drug Administration (FDA) to its "do not use" hand sanitizer list, along with one warning letter.
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