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76 Results
Section: Regulations > Regional
Claims/Labeling
Study Reports VapoRub to Cause Breathing Issues in Infants
Vicks VapoRub, a popular topical congestion remedy, was reported to cause airway inflammation, resulting in restricted breathing in infants and toddlers, according to a study by Wake Forest University.
Regional
FDA Clarifies Executive Summary on Talc is Solely to Solicit Data
In response to concerns that the FDA's Executive Summary on talc could be interpreted as official recommendations, the agency clarified this summary is solely intended to solicit scientific information.
Safety/Stability
Why the FDA's 'Sunscreens in the Bloodstream' Study is Flawed
A recent study published in the
Journal of the American Medical Association
tested the potential systemic absorption of certain sunscreens. Results identified their presence in subjects' bloodstreams; however, as industry expert David Steinberg explains, the study is misleading and fails to consider crucial variables.
Regional
US Regulations Update: FDA Issues Final Monograph for Skin Protectants
On June 4, 2003, the FDA published the Final Monograph (FM) for Skin Protectant Drugs for Human Use.
Regional
FDA Issues Draft Guidance for Cosmetics Company Product Registration and Submission
The draft guidance is intended to help ensure the safety of cosmetic products that many consumers use day-to-day. The FDA is accepting comments on the draft guidance until Sept. 7.
Regional
SCCP Reviews Hair Dyes
In Europe, the Scientific Committee on Consumer Products (SCCP) has been busy reviewing the components of hair dyes. On Dec. 13, 2005, the committee issued its opinion on the exposure and reaction products of oxidative hair dye formulations. For chemists interested in the chemistry of oxidative hair dyes, this is an excellent review of the various chemical reactions that result in hair dyeing.
SPF/Sun
Could the US Virgin Islands Be Next to Ban Octinoxate and Oxybenzone?
A bill banning the sale, importation and distribution of certain sunscreen ingredients in personal care is making its way through the U.S. Virgin Islands' legislature.
Regional
After 8+ Years, is Canada Ready to Ban Animal Testing for Cosmetics?
Health Canada confirmed plans are in the works to implement an animal testing ban for cosmetics, according to The Globe and Mail.
Tech/Equipment/Services
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.
Hair Care
Hair Dyes On the Block
As part of the Cosmetic Directive, the European Commission may ban seven non-permanant.
Regional
Hair Dye Ingredients In Question
Henna and hair dye may be in trouble.
Regional
22 Hair Dye Substances Banned
As part of its hair dye strategy, the European Commission has banned 22 hair dye substances...
Claims/Labeling
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.
Regional
Update: TSCA Reform Bill is Trying to Make its Way to President's Desk
A bill that amends the Toxic Substances Control Act (TSCA) to revise regulations on chemicals has passed the House although what is next now remains in question.
Regional
Brazilian PBA Warns Consumers About Hair Treatment
The Professional Beauty Association (PBA) of Brazil has alerted consumers to the danger of using Brazilian keratine treatments and/or Escova progressiva treatments.
Claims/Labeling
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).
SPF/Sun
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.
Natural/Sustainable
Taking Hair and Scalp Care to New Heights
This issue of
C&T
is at the forefront of hair/scalp science, exploring test methods, trends and innovations. It also revisits the fundamentals of formulating with ZnO, for mineral sunscreens, and presents an upcycled tea extract to counteract photodamage.
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