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Section: Regulations

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P&G Detects Benzene in Antiperspirant and Body Sprays, Issues Recall

P&G has voluntarily recalled specific lots of Old Spice and Secret aerosol spray antiperspirants and Old Spice Below Deck aerosol spray products due to the detection of benzene.

Johann W. Wiechers, Ph.D.

Words from Wiechers: The Term Cosmeceuticals is No Longer Sustainable

"We really cannot differentiate between a cosmetic and a drug if we accept the fact that a claim made for the product can determine to which category it belongs," Wiechers criticizes, in this "Words from Wiechers."

China could be phasing out animal testing for many cosmetic categories.

Is China Ending Pre-market Animal Testing for Cosmetics?

Hair dye, sunscreen and select other products would be exempted.

China Sees Contamination and Product Recall Issues with Exports

China is undoubtedly one of the biggest cosmetic and personal care manufacturers in the world. However, it has been experiencing product recall and contamination issues with exported goods over the last six months.

Establishing the Dividing Line: Is Your Product a Drug?

To avoid regulatory penalties, a company developing an OTC product must institute properly administered shelf-life testing programs as an integral part of its product development and marketing efforts.

Anti-polllution claims are only made by about 1% of beauty products on the market, representing a massive opportunity for market innovation.

Is Your Brand Making Anti-pollution Claims? Read This.

New free in-depth report outlines the growth opportunities and challenges of infusing beauty brands with anti-pollution claims.

The European Regulation for Cosmetics: Who is the Responsible Person?

The Cosmetics Regulation (EC) No 1223/20091 is the main regulatory framework for finished products when placed on the EU market and introduces the notion of the responsible person.

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[podcast] Sustainable Isn't Enough: How Beauty Brands Can Be Authentic

What's missing from the sustainability story? The "people piece," at least according to Giorgio Dell'Acqua, Ph.D. The problem is the industry needs a credible metric to measure its social impact. Hear more in this podcast.

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.

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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.

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.

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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.

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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.

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.

Mind Over Matter: Cosmetic Claim Substantiation Issues Facing the Future

It is generally accepted by the public that effective cosmetic products can positively influence the well-being of individual consumers. Whereas we can easily measure the skin moisturizing properties of a cosmetic formulation, measuring its precise effects on well-being is much more complex.

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.

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.

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FDA Flags 13 More Sanitizers, Issues One Warning for Methanol Content

Methanol content or possible associations therewith account for 12 of the 13 latest additions by the U.S. Food and Drug Administration (FDA) to its "do not use" hand sanitizer list, along with one warning letter.

The Issues Common With Trending Natural Ingredients: The Pitfalls of Naturals

The ever-evolving nature of skin care presents ongoing challenges for marketing claims and labeling. Here are a few things to watch out for.

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