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Recent in Regulatory (page 14 of 22)
May 6, 2014
Over the past 25 years, no category of “cosmetics” has seen change like sunscreens. This discussion reviews how current regulations have come to be, and looks to where they are headed.
Apr 21, 2014
Cosmetic companies comply with strict ingredient regulations and stay abreast of the latest scientific studies to ensure that their products are safe and efficacious. Yet, rumors still abound about cosmetic companies intentionally including toxic chemicals. This column looks into those myths, separating fact from fiction.
Apr 14, 2014
In March 2014, the PASS Coalition published its support of a proposed Act to potentially speed the FDA's approval of new UV filters. In a related blog post, PASS followers congratulated those involved, and urged Canadian regulators to do the same.
Mar 28, 2014
Independent Cosmetic Manufacturers and Distrubutors (ICMAD) board member Craig Weiss, president of Consumer Product Testing, testified on March 25, 2014, during recent U.S. Food and Drug Administration (FDA) hearings on modernizing over-the-counter drugs.
Mar 20, 2014
This column is the first in a two-part series on importing cosmetics into Japan. It discusses the general requirements for cosmetic manufacturers and distributors. The second part discusses these requirements in more depth, and provides a closer look at sunscreen requirements.
Mar 20, 2014
This column is the second in a two-part series on importing cosmetics into Japan. It discusses the requirements for cosmetic manufacturers and distributors in more depth than the first part, and provides a closer look at sunscreen requirements in Japan.
Mar 18, 2014
On Mar. 13, 2014, U.S. Senator Jack Reed (D-RI) and U.S. Congressman Ed Whitfield (R-KY) introduced the bipartisan, bicameral Sunscreen Innovation Act (S. 2141 and H.R. 4250, respectively), which has been supported by the Public Access to SunScreen (PASS) Coalition.
Mar 12, 2014
The Humane Cosmetics Act, introduced by Congressman Jim Moran, would make it unlawful for anyone to conduct or commission cosmetic animal testing in the U.S. and prohibit selling, offering for sale or transporting any cosmetics in interstate commerce if the final product or any component was developed or manufactured using animal testing.
Mar 10, 2014
On Mar. 6, 2014, Michael Taylor, on behalf of th The U.S. Food and Drug Administration (FDA), responded to the Proposed Draft Legislation by the Personal Care Product's Council (PCPC) and the Independent Cosmetics Manufacturers and Distributors (ICMAD), effectively finding no common ground between the three and closing the negotiation.
Mar 10, 2014
The plan includes full disclosure of all ingredients including those typically protected under trade secrets such as fragrances.
Mar 3, 2014
The end of February was busy for the U.S. Food and Drug Administration (FDA), which published two letters on the Time and Extent Applications (TEAs) for diethylhexyl butamido triazone (Uvasorb HEB) and amiloxate (Neo Heliopan E 1000), finding insufficient scientific evidence to claim either as generally recognized as safe and effective (GRASE) and denying their addition to the OTC Sunscreen Monograph.
Feb 21, 2014
Methylisothiazolinone (MI or MIT), a preservative used in cosmetics and other household products, has recently been in the news. MI was approved in Annex V as a cosmetic preservative up to 0.01%; however, after dermatologists found it to be a possible allergen, its safety was again reviewed by the SCCS.