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The Requirements for Fragrances Used in Cosmetics in America
According to FDA regulations, if a product is intended to be applied to a person’s body to make the person more attractive, it’s a cosmetic under the law, for instance perfumes, colognes and aftershave should all be regulated as cosmetics. However, some products add fragrances for therapeutic purposes, such as aromatherapy products that could relieve muscle pain or headaches, and fragrance products that help sleep. These kind of fragrance products are generally regulated as pharmaceuticals. Other products that may contain fragrance ingredients, but are not applied to the body, including detergent, fabric softener and carpet freshenerare, are under the administration of the Consumer Product Safety Commission.
United States
Cosmetic Ingredient
Cosmetic Label
The Requirements for Fragrances Used in Cosmetics in America
United States
Cosmetic Ingredient
Cosmetic Label
US FDA Publishes Structured Product Labeling (SPL) Implementation Guide
The US Food and Drug Administration has published a Structured Product Labeling (SPL) Implementation Guide with Validation Procedures. Cosmetic product facility registrations and product listings are now included within the SPL framework. The Implementation Guide can be used to develop SPL authoring tools. In the future, once FDA begins accepting data, users may transmit SPL-formatted submissions through FDA’s Electronic Submissions Gateway (ESG), or SPL authoring software including Xforms, for cosmetic product facility registrations and product listings, mandated by the Modernization of Cosmetics Regulation Act of 2022 (MoCRA).
United States
Cosmetics
US FDA Publishes Structured Product Labeling (SPL) Implementation Guide
United States
Cosmetics
Frequently Asked Questions (FAQs) about the US FEI Portal
The US FEI Portal allows a user to look up an FDA Establishment Identifier (FEI) based on a firm name and address, or validate the address of an FEI.
United States
Cosmetics
Q&A
Frequently Asked Questions (FAQs) about the US FEI Portal
United States
Cosmetics
Q&A
US FDA Issued Draft Guidance on Registration and Listing of Cosmetic Product Facilities and Products
On August 7, 2023, the US Food and Drug Administration (FDA) published draft guidance on cosmetic product facility registrations and product listings, as mandated by the Modernization of Cosmetics Regulation Act of 2022 (MoCRA).
When finalized, the draft guidance will assist stakeholders with cosmetic product facility registration and product listing submissions to FDA, by describing who is responsible for making the registration and listing submissions, what information to include, how to submit, and when to submit, as well as certain exemptions to the registration and listing requirements.
United States
Cosmetics
The Use of 1,4-dioxane or Mercury in Cosmetics and Personal Care Products is Prohibited in New York State
In December 2022, Hochul, governor of New York State, signed an amendment to the Environmental Protection Act (A8630A) to prohibit the use of 1,4-dioxane or mercury in cosmetics and personal care products. The bill will come into effect on June 1, 2023. From the effective date, cosmetics or personal care products containing 1,4-dioxane or mercury must not be sold in New York State.
United States
Cosmetics
Cosmetic Ingredient
The Use of 1,4-dioxane or Mercury in Cosmetics and Personal Care Products is Prohibited in New York State
United States
Cosmetics
Cosmetic Ingredient
Major Changes to US Cosmetic Regulations — Cosmetics Registration and Filing will be Mandatory!
On December 29, 2022, US President Biden signed into law the Food and Drug Omnibus Reform Act (FDORA Act), which included the Modernization of Cosmetics Regulation Act of 2022 (MOCRA Act). This is the first significant amendment to American cosmetics regulations since 1938.
Compared with the current Federal Food, Drug and Cosmetic Act (FDC Act), MOCRA Act forces cosmetic enterprises to register their facilities and maintain records for their products.
United States
Cosmetics
The Requirements for International Cosmetic Packaging and Labeling
There is a diverse range of cosmetic packaging materials, such as glass, metal, plastic, and soft paper packaging. As the last process in the modern cosmetics industry, packaging is necessary to keep the contents clean and safe. However, it is also important to make sure the packaging itself does not pollute the cosmetics or add any unsafe factors to the contents. In addition, consumers’ understanding and judgment of cosmetics products often relies on the information provided on the products and by the sellers, the display of such information, to a large extent, determines consumers’ purchasing decisions and use methods for products.
China
Japan
European Union
Korea
United States
Cosmetic Label
The Requirements for International Cosmetic Packaging and Labeling
China
Japan
European Union
Korea
United States
Cosmetic Label
CIRS Attended ICMAD and PCPC Panel Discussion Regarding International Cosmetics Regulations
On 29 Jul. 2019, ICMAD and PCPC jointly held a panel discussion regarding the hot topics of China, US and Canada cosmetics regulations in Cosmoprof North America. The top concerns include but not limited to animal testing ban, environmental impact of sunscreen ingredients, ingredients disclosure, etc. During the panel discussion, CIRS shared the latest info of China cosmetics regulations including the filing status of imported non-special use cosmetics at different local MPA
United States
CIRS Attended the Annual Meeting of the Personal Care Products Council
On February 24-27th, 2019, the annual meeting of the Personal Care Products Council (PCPC) was held in West Palm Beach, Florida. April Guo, General Manager of Personal Care Division of CIRS, was invited as the guest speaker. The PCPC is the leading national trade association representing cosmetic and personal care products companies that has more than 600 member companies represent more than 90 percent of the U.S. beauty industry. The PCPC annual meeting is the largest gathe
United States
CIRS Attended the ICMAD Cosmetic Technical/Regulatory Forum
February 19-20th, 2019, ICMAD Technical/Regulatory Forum was held in Los Angeles, USA by the Independent Cosmetics Manufacturers and Distributors (ICMAD). Ms. April Guo, General Manager of Personal Care Division of CIRS, was invited as the guest speaker. Since 1974, ICMAD has provided essential guidance and support through business tools, publications, education, networking opportunities, and key advocacy support. ICMAD Technical/Regulatory Forum has a history of 14 years, w
United States
China Cosmetic Registration and Filing
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China New Cosmetic Ingredient Registration and Filing
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China Cosmetic Ingredient Quality and Safety Information Code Application
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China Cosmetics Safety and Efficacy Test
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Cosmetics Notification in South Korea
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Functional Cosmetics Notification in South Korea
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China Cosmetic Registration and Filing
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China New Cosmetic Ingredient Registration and Filing
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China Cosmetic Ingredient Quality and Safety Information Code Application
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China Cosmetics Safety and Efficacy Test
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Cosmetics Notification in South Korea
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Functional Cosmetics Notification in South Korea
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