Search Cosmetics & Toiletries: Page 23

460 Results

Section: Regulations

Fotolia_78563935_Subscripti

Expansion and Challenges Ahead for Emerging Markets: Growth in Natural Skin Care

Natural/organic brands need more than just natural credentials to attract consumers’ attention. Many have already launched more sophisticated products, such as anti-aging products and serums with strong claims.

ACI and PCPC Form Coalition to Promote Antibacterial Use to the FDA

The Personal Care Products Council (PCPC) and the American Cleaning Institute (ACI), which have formed the Topical Antimicrobial Coalition, have submitted their comments to the U.S. Food and Drug Administration (FDA) regarding its proposed rule, which they find could elliminate access to antibacterial soaps and increase foodborne illness.

PASS Coalition and Congressman Sam Farr Press FDA for UV Filter Approval

The PASS Coalition expresses its gratitude to subcommittee ranking member Sam Farr (D-CA) for pressing the FDA about the approval of pending sunscreen ingredients but notes that some UV filters have been pending with the FDA for over a decade.

According to the European Commission's Safety Gate, numerous products, ranging from soaps and fragrances, to body care, shampoo, bath milk and others, have been flagged for the present of the fragrance allergen butylphenyl methylpropional.

Recall Alert: L'Oreal's Mizani, J&J's Clean & Clear, Marcelle's 40+ Cream and Others

Globally, within the past couple of months, numerous cosmetic product recalls have been issued for microbe contamination and fragrance allergens, among other contaminants. Following is a roundup.

This article provides regulatory updates primarily in China and India, as well as Thailand and South Korea. Topics include formula submissions, new ingredients/safety, Korean standards, India cosmetics rules and more.

Formulas, New Ingredients/Safety, South Korean Standards, India Rules 2020 and More

This article provides regulatory updates primarily in China and India, as well as Thailand and South Korea. Topics include formula submissions, new ingredients/safety, Korean standards, India cosmetics rules and more.

HandSanitizerBackLabel_850x425

FDA 'Do Not Use' Hand Sanitizer List and Methanol, 1-Propanol Warnings

The U.S. Food and Drug Administration (FDA) has issued a guide for consumers to explain the dangers of methanol and 1-propanol, and to search and find hand sanitizers on its "do not use" list; some 165 entries are on it so far.

Proposals for the restriction of PFAS will be accepted by the ECHA through Sept. 25, 2023.

ECHA Updates: 8 Chemicals for REACH Authorization and Call for PFAS Proposals

The ECHA proposed adding eight chemicals to the REACH Authorization list, including some cosmetic ingredients. The agency also is calling for PFAS proposals, and it shared consultations on conforming restriction proposals and SEAC draft opinions.

LabManufacturingQAQC850x425

Is Your Microbiology Lab FDA-compliant? Part I: Personnel, Facilities and Equipment

This two-part article provides an overview of areas relevant to the U.S. Food and Drug Administration’s (FDA’s) inspection of cosmetic microbiology laboratories. Part II will appear in our July 2018 edition.

Recent stories from the FDA include 5000 lbs of eye shadow that were seized en route to Washington state, Unilever recalling dry shampoo and the appointment of Norman Birenbaum in the FDA.

FDA Roundup: Cosmetics Seized, Unilever Recall, Cannabis/Public Health Hire and More

Recent stories from the U.S. Food and Drug Administration include: 5,000 lbs of eye shadow seized en route to Washington state, Unilever recalling dry shampoo, the appointment of cannabis expert Norman Birenbaum as public health advisor, and more.

Na True Takes Steps to Define Natural and Organic Personal Care

Recently, Na True published a definition for natural and organic cosmetics as well as criteria for a three-tiered label system that is expected to become valid throughout Europe.

850_beautyclaimsboxes

FDA Claims Warnings Strike Again: Using Terms 'Botox-like' and More

Once again, U.S. regulators are cracking down on beauty companies that have crossed over into unapproved drug claim territory based on how they are promoting their products online.

REACH Update: Exposure Scenario Annexes and Other Changes to the SDS

The statutory basis for safety data sheets (SDSs) is laid down in Article 31 of REACH, and Annex II details the requirements for the compilation of an SDS in accordance with this article.

Sunscreens_Epstein_850X425

[podcast] Sunscreen Innovation Act Update: MUsT Test and Penetration Potential

"What’s changed with respect to sunscreen evaluation is ... the test model they are using now is designed for drugs ...and has never been applied previously for the sunscreens," Epstein reports.

Dreamstime M 16934378 Womandyeinghair

FDA Updates: VCRP Tally, Color Additives and Lead Acetate in Hair Dyes

The U.S. Food and Drug Administration (FDA) provides the latest tally on voluntarily registered cosmetics, color additives and lead acetate in this collective fall 2021 update.

EuropeanUnionMapStarsFlag850x425

EU's Chemical Strategy for Sustainability to Rewrite Cosmetics Regulation and Risk Management

"...Centralizing chemical reviews and promoting risk-management uniformity across sectors make Cosmetics Europe believe cosmetics regulatory changes lie ahead."

New U.S. UV Filters and the Cosmetic Outlook in Canada for Sunscreens

Skin cancer is the most common cancer today, but only recently has industry pressure and political leadership compelled changes in the North American regulatory paradigm of sunscreen products. The passage of the Sunscreen Innovation Act in the United States and the suggestion to regulate sunscreens as cosmetics in Canada would give regulators the tools to reboot a stalled approval system.

Regulatory Review—Cosmetic Ingredient Update: The Ugly, the Good and the Bad

This review takes a look at updates to ingredient regulations as of the first quarter in 2012. While “the ugly” refers to the EU Chemical Agency’s (ECHA’s) release of the first ingredients to be evaluated under REACH, the good news relates to the battle in Canada to save D5. “The bad” are the state of California’s addition of three ingredients to the Proposition 65 list, as well as Health Canada’s caution against labeling using generic terms.

The Regulatory Interface: When is it a Cosmetic and When a Drug?

Both the cosmetic industry and the Food and Drug Administration (FDA) have had a long and interesting history. FDA’s history began in 1906 with the enactment of the Pure Food and Drug Act. This was the first attempt to regulate the safety of products (or additives). For almost 100 years Congress has set the standards and published them in the United States Code (USC). FDA and other federal agencies promulgate regulations through notice and comment rulemaking. Proposed regulations are published in the Federal Register (FR) and the public is given an opportunity to comment. The agencies then publish in the Federal Register final regulations together with a preamble discussing each comment. Industry and regulatory scientists eagerly follow these changes and access them on the Web. Final regulations are compiled in the Code of Federal Regulations (CFR).

Page 23 of 26