Search Cosmetics & Toiletries: Page 9

375 Results

Section: Regulations

NAD Urges Cessation of Botox-like Claims for One Antiwrinkle Product

The National Advertising Division (NAD) has recommended that the Botox-like claims made for one OTC wrinkle treatment be discontinued after the test data submitted was deemed insufficient.

CTPA Responds to Report on Cosmetics Blocking Androgens in Male Fetuses

The Cosmetic, Toiletry and Perfumery Association (CTPA) has responded to reports questioning the safety of perfumes and scented body lotion for unborn males.

Farah K. Ahmed, president and CEO of Fragrance Creators Association, issued a statement recognizing the passing of California’s Menstrual Products Right to Know Act of 2020 (AB 1989).

Fragrance Creators Issues Statement on California’s Menstrual Products Right to Know Act

"Fragrance Creators engaged in a constructive dialogue with all stakeholders to ensure clarity and consistency across products so that consumers can make informed product selections and comparisons," states Farah K. Ahmed, president and CEO, Fragrance Creators.

pigments in tins powder stacked turned

Fees Increased on U.S. FDA Color Additive Certification; Here's What You'll Pay

"The color certification process for synthetic organic colorants is an important aspect of color additive regulations that is unique to the United States," notes industry expert Kelly Dobos. "This fee had remarkably not been raised in nearly 20 years."

With an increase in sustainability, consumer focus and particularities from consumers about health concerns, the press release from PASS furthers the discussion of regulations in sunscreen and other application products.

PASS Weighs in on NAS Report Finding Insufficient Data for Sunscreen Bans

Responding to increased interest in sustainability and consumer health concerns, the Public Access to SunScreens (PASS) Coalition released a statement responding to recent NAS findings and furthering the discussion of regulations in sunscreens.

YoungGirlApplyingBlush850x425

Dingell, EWG to Press for Legal Action on Children's Makeup, Asbestos Allegations

Congresswoman Debbie Dingell and representatives of the EWG will pressure Congress to pass legislation protecting children from alleged asbestos-containing makeup. To this end, a press call will be held on Jan. 17, 2020, at 11:00 a.m. EST.

The announcement from the government is an important step towards the goal of ensuring that non-animal methods are accepted by the authorities to meet the requirements of other pieces of UK chemicals legislation, per the CTPA.

CTPA Welcomes UK Government Action to Ensure No Cosmetic Ingredient Testing on Animals

The announcement from the government is an important step towards the goal of ensuring that non-animal methods are accepted by the authorities to meet the requirements of other pieces of UK chemicals legislation, per the CTPA.

CT.com_deodorant

CTPA Says Review Paper on AP/Deo, Breast Cancer Should Not Cause Alarm

A recent paper calling for further research into the alleged link between aluminium salts in antiperspirants and breast cancer should not constitute alarm, said the CTPA.

TCS_ingredient.label

AAD Responds to FDA Labeling Decision on Eczema Medications [Feb. 21, 2006]

The American Academy of Dermatology (AAD) recently issued a statement in response to the U.S. Food and Drug Administration’s (FDA) decision that a black box warning be added to labels...

woman wearing yellow eyes closed applying sunscreen to face outdoors

Has DSM-Firmenich Put Us on a Path to a New U.S. Sunscreen Approval?

DSM-Firmenich has submitted its Parsol Shield (INCI: Bemotrizinol) UV filter to the FDA for review in hopes of earning it a GRASE status and inclusion in the U.S. OTC Sunscreen Monograph. This would be the first new sunscreen added in 25 years.

850x425_icmad-cosmetics-regulation

ICMAD President and CEO Releases Statement on Modernization of Cosmetics Regulation Act of 2018

ICMAD president and CEO Pam Busiek notes that the organization has begun reviewing the draft legislation, and will provide feedback by the deadline.

Farah K. Ahmed, president and CEO of Fragrance Creators Association, issued a statement recognizing the passing of California’s Cosmetic Fragrance and Flavor Ingredient Right to Know Act of 2020 (SB 312).

Fragrance Creators CEO Issues Statement on Cosmetic Fragrance and Flavor Ingredient Right to Know Act

Farah K. Ahmed, president and CEO of Fragrance Creators Association, issued a statement recognizing the passing of California’s Cosmetic Fragrance and Flavor Ingredient Right to Know Act of 2020 (SB 312).

A total ban across the entire class of PFAS would be disruptive without any basis in science. A more deliberate approach would better suit public policy.

Why a Ban on PFAS Across Cosmetics and Other Industries Right Now is Misguided [opinion]

The wide use of forever chemicals across cosmetics and other industries and their persistence have opened them to scrutiny. But banning the entire PFAS class would be disruptive without any basis in science or good public policy. Why? Read on to see.

The guides are regularly revised to incorporate the progress of scientific knowledge in general and the experience gained particularly in the field of testing and safety evaluation of cosmetic ingredients.

11 Changes to SCCS Guides for Cosmetics Safety Testing — Plus a Note on 'Nano'

The European Union's (EU's) Scientific Committee on Consumer Safety (SCCS) recently updated its notes of guidance (NoG) for cosmetics and cosmetic ingredient safety testing, emphasizing alternatives to animal testing and more.

Fda Mocra Story Fragrance Allergens Authority Adobe Stock 753447517

[interview] U.S. FDA on MoCRA: New Authority, Fragrance Allergens, Animal Testing and More

In this interview, the FDA describes its new MoCRA-mandated authorities, 5 requirements for industry (and how it will enforce them), the mandate for listing fragrance allergens, why animal testing was omitted from MoCRA and more.

A responsible person is required to report serious adverse events associated with the use of cosmetic products in the U.S. to FDA within 15 business days.

FDA Releases Update to Ongoing Activities Related to Serious Adverse Event Reporting for MoCRA

A responsible person is required to report serious adverse events associated with the use of cosmetic products in the U.S. to FDA within 15 business days.

FDA Publishes Opinion on Two Sunscreen TEAs and Is Urged for More Action by PASS

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.

The U.S. Food and Drug Administration (FDA) has issued stern warnings regarding methylene chloride, a banned substance detected in four gel nail polish removers.

Regulation and Safety Update: Methylene Chloride in Nail Products, Europe on PFAS, U.S. Recall Alerts and Talc Settlement Setback

This roundup highlights recent headlines in cosmetic safety and regulations, including FDA alerts on banned substances in nail products and efforts in the EU and France to curb PFAS. Updates on talc and recalled products are also noted.

Page 9 of 21