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Section: Regulations

Comparatively Speaking: Trademarks, Principal Register vs. Supplement Register

The Principal Register grants benefits to registered trademarks; the Supplemental Register is primarily designed for marks to distinguish the applicant's goods or services

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Back to Basics: Making Room for Regulatory Compliance

Developing a cosmetic product requires an extensive, multistep process. This article introduces a multiple-part primer of the cosmetic development process, and stresses the importance of keeping up with compliance protocols.

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VIDEO: CONUSBAT's Struessmann Comments on Innovation in Cosmetics

Dr. Annelie Struessmann comments on the need for innovation in the cosmetics and personal care industry.

Consumers Becoming More Discerning on Companies' Greening Claims

An increase in customer relations and sincerity during the implementation in the green trend, which continues to grow, is necessary to further development consumer trust, says the Natural Marketing Institute.

European Commission Approves Fentanyl HCl Iontophoretic Transdermal System

The European Commission has granted marketing authorization in the 25 member states of the European Union for the use of Fentanyl hydrochloride (HCl) Iontophoretic Transdermal System (ITS) 40 mcg/dose...

Company Recalls Acne Gels Due to Bacteria Threat

The company recalled 1 ounce (28 g) tubes of DG Maximum Strength Acne Medicated Gel, sold at Dollar General; Kroger Acne Gel 10% Benzoyl Peroxide Acne Medication, sold at Kroger; and Equate: Medicated Acne Gel, sold at Wal-Mart.

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FDA Extends Comment Period for Proposed Sunscreen Rule

Extension to run through Dec. 26, 2007; agency seeks to balance industry concerns and the interests of public health to ensure that sunscreen products properly inform consumers of the level of protection.

REACH Update: ECHA Urges Companies to Organize SIEFs

In a fact sheet dated Apr. 24, 2009, the ECHA reminded REACH preregistrants that it is urgent to become involved in SIEF activities as soon as possible since deadlines for registration are extremely tight.

Hear more on this topic at Beauty Accelerate Virtual. $89 for 4 days, as of Oct. 7. See details below.

Beauty Accelerate Virtual: Fragrance Allergens—Are You Compliant?

During Beauty Accelerate Virtual, Luke Grocholl, Ph.D., of MilliporeSigma, will detail regulatory requirements and guidelines that impact fragrance ingredient selection, as well as label requirements for key ingredients.

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Pilot Chemical Company Earns Responsible Care Certification

This certification is used to demonstrate the company’s commitment to the highest standards of health, safety, security and environmental performance for both products and operations.

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Second Nature: Sustainability as the Outgrowth of Naturals, A Commentary

Personal care consumers increasingly demand natural products but these are not always sustainable, especially considering the broader principles of this doctrine. This paper is a commentary on natural products and ingredients, certifications and innovations to advance this category in the context of UN Sustainable Development Goals.

Exclusive! Comparatively Speaking: Drugs vs. Cosmetics by Tony O'Lenick

Tony O’Lenick asks: What is the difference between a drug and cosmetic? David Steinberg explains.

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Microbiological Considerations for Refillable Bulk Cosmetics: Survey and Commentary

The commercial sale of refillable products in bulk now includes liquid galenic formulas. Their diverse flow chains pose unique microbial challenges, as shown here, underlining the importance of flow chain planning and assessment tools/strategies.

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FDA Warns CBD Company Making Unsubstantiated Marketing Claims

The agency has issued a warning letter to Curaleaf Inc., for illegally selling unapproved products containing cannabidiol (CBD) online. The company is accused of making unsubstantiated claims that the products treat cancer, Alzheimer’s disease and opioid withdrawal, among other conditions or diseases.

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Diatomaceous Earth and Comfrey Root Catch the FDA's Eye

This is a good reminder for cosmetic manufacturers to be careful when straddling the line between a cosmetic and drug. It's all in the claims.

Comparatively Speaking: US FDA Categories of Hand Sanitizer Actives

Anthony J. O’Lenick, Jr. turns to David R. Macinga, PhD, and James W. Arbogast, PhD, to explain the differences between the US FDA categories used to classify hand sanitizer actives.

PCPC Responds to CDC's Request for Skin Cancer Comments

The Personal Care Products Council's (PCPC) Farah Ahmed submitted comments to the Centers for Disease Control and Prevention (CDC) in response to the CDC’s request for information about reducing exposure to UV radiation in order to reduce skin cancer rates.

Challenges in Creating NPA- and WFM-compliant Natural Formulations

Where does the formulation chemist begin when facing a marketing request for a product stamped with a “natural” label claim? The first step is to identify the certifying organization or government under which the formulation is to be sold, followed by the choice of preservatives. The basic approach to composing natural products is outlined here.

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