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Section: Regulations > Regional
Regional
FDA Flags Eskbiochem Hand Sanitizers for Possible Methanol Content
The U.S. Food and Drug Administration has issued a warning statement to consumers over the use of Eskbiochem's hand sanitizers, which may contain methanol, i.e., wood alcohol.
Claims/Labeling
ICMAD Responds to Suit Against FDA Over Nanotechnology
In response to the suit filed against the US Food and Drug Administration (FDA) by a coalition of six consumer safety and environmental groups over the FDA's lack of nanotechnology regulation, Independent Cosmetic Manufacturers & Distributors (ICMAD) has sent an exclusive response to
Cosmetics & Toiletries
magazine, as shown here.
Regional
FDA Recalls Face Paint Due to Adverse Reactions
The FDA has learned of a cluster of adverse events in children exposed to various colors of the face paint. All exposures occurred on the same day at an organized event and included rashes, itchiness, burning sensation, and swelling where the face paints were applied.
Claims/Labeling
Talcum and Toxins Lawsuit Escalates, FDA Calls Meeting on Talc Testing
Several major talcum powder marketers are being slapped with a new lawsuit alleging their products contain undisclosed dangerous substances. In relation, the U.S. FDA has called a public meeting, to be held on Feb. 4, 2020, regarding testing for asbestos in talc and talc-containing cosmetic products.
Regional
[update] FDA April Meeting for June ICCR-14 Meeting Cancelled
In light of the COVID-19 outbreak, the FDA has cancelled the public meeting originally scheduled for April 14, 2020, to discuss topics for the international ICCR-14 meeting on cosmetics regulation, still planned (thus far) to be held from June 8 to June 10, 2020.
Regional
[updated] FDA Oversight Becomes Closer to Reality for US Cosmetics
According to the bill's authors, it is supported by the leading cosmetic manufacturers and would give the FDA unprecedented authority.
Editor's note: This report now includes CIR commentary.
Regional
Cosmetics Registration in California and the FDA's Electronic-only Drug Registration
The stars where poorly aligned on June 15, 2009, when California finally issued its registration procedure and forms for the California Safe Cosmetics Act of 2005. At the same time, the US Food and Drug Administration (FDA) moved to an electronic-only filing system for drug registrations. These two changes have created significantly more work for the personal care industry—and with questionable benefits.
Claims/Labeling
Diatomaceous Earth and Comfrey Root Catch the FDA's Eye
This is a good reminder for cosmetic manufacturers to be careful when straddling the line between a cosmetic and drug. It's all in the claims.
Regional
US FDA Plans First Cosmetic Allergen Survey in Decades
The proposed survey is meant to help the organization better understand adverse events caused by allergens in cosmetics, and is the first of its kind since 1975.
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.
Claims/Labeling
FDA Issues Warning Letter for Eyebrow/Eyelash Growth Product Claims
Cosmetic manufacturer Lifetech Resources LLC has been issued a warning letter by the US Food and Drug Administration (FDA) regarding claims touted on three of its eye care products.
Regional
Dermatology Association Urges FDA to Postpone Program for Isotretinoin Patients
Patient safety while taking isotretinoin depends on the careful oversight of the prescriber, according to the American Academy of Dermatology Association.
Regional
FDA Calls Out Contaminants, Methanol and Packaging in Latest Alerts
Methanol content, yeast contamination and packaging resembling beverage bottles are among the U.S. Food and Drug Administration's latest hand sanitizer and product recall alerts.
Regional
FDA Flags 12 Companies for Illicit Hydroquinone-containing Skin Brighteners
The products contain the active drug hydroquinone, rendering them unapproved over-the-counter (OTC) drugs rather than cosmetics.
Regional
FDA Cautions: Hair-smoothing Products Can Release Formaldehyde
The U.S. Food and Drug Administration recently released a statement warning users of the potential for hair-straightening products to release formaldehyde gas, a known carcinogen, during heat treatments.
Regional
US FDA to Assess Cosmetic Safety Through Manufacturing Survey
The survey "is part of the FDA’s ongoing effort to add to [its] understanding of the cosmetic industry and manufacturing practices" in order to ensure cosmetic safety.
Regional
Industry Stakeholders Back the FDA to Modernize Cosmetic Regulations
Recently, the Personal Care Products Council, Fragrance Creators Association, Independent Beauty Association and Consumer Healthcare Products Association declared their support for modernizing cosmetic regulations in a letter to the FDA.
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.
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