Medical device color additives play a vital role in ensuring safety, usability, and compliance in healthcare products. Therefore, understanding their classification, purposes, and regulatory requirements is crucial for manufacturers aiming to meet FDA standards. In this article, UCC will provide an in-depth look into medical device color additive, highlighting key details for compliance, safety, and […]
Author Archives: thaohien
For businesses involved in the production or distribution of medical devices in the United States, ensuring compliance with the FDA’s registration and listing requirements is essential. In this article, UCC will provide an overview of the process, with a particular focus on the FDA product code list for medical devices and how to properly list […]
The FDA’s Medical Device Unique Identifier (UDI) system provides a standardized method to identify and track medical devices throughout their lifecycle. As a result, by using UDI, manufacturers, healthcare providers, and patients ensure better safety, traceability, and accountability. In this article, UCC will outline UDI, its components, and key requirements for manufacturers and stakeholders. 1. […]
The California Safe Cosmetics Program (CSCP), established in 2005, is a regulatory framework aimed at ensuring the safety of cosmetics sold in California. As the first state in the U.S. to implement such regulations, California requires cosmetic brands to report any ingredients that may pose a risk to consumer health. Therefore, in this article, UCC […]
Good Manufacturing Practices (GMP) are essential for ensuring product quality, safety, and consistency in manufacturing and distribution. In today’s regulated markets, adhering to GMP is crucial for meeting both consumer expectations and legal requirements. In this article, UCC will outline the key components of Mocra GMP and its significance for businesses, particularly those in the […]
With the introduction of the Modernization of Cosmetics Regulation Act (MoCRA), cosmetic businesses seeking to enter the U.S. market are now required to adhere to updated regulatory standards. Additionally, a key provision of this legislation mandates the listing of cosmetic products with the FDA. In this article, UCC will provide a detailed explanation of the […]
In the world of cosmetics, labeling plays a crucial role in communicating a product’s benefits to consumers. Claims such as “Cruelty-Free” and “Alcohol-Free” are commonly seen on product labels. However, many people wonder whether these claims are regulated by the FDA. In this article, UCC will explain the essentials of cosmetics labeling claims and provide […]
When it comes to cosmetic products, proper labeling is crucial for ensuring consumer safety and compliance with regulations. The FDA (Food and Drug Administration) has specific guidelines for cosmetic ingredient labeling, and it is essential for manufacturers and distributors to adhere to these standards. In this article, UCC will explore the key requirements for FDA […]
In the cosmetic industry, safety is a top priority. As consumer demand grows, brands must follow strict regulations to ensure safety and transparency. A key part of this compliance is the proper use of cosmetic warning labels. These labels are required by law and help inform consumers of potential risks. In this article, UCC will […]
Fragrance allergens have become a growing concern in the cosmetic industry, particularly for individuals with sensitivities. Understanding the requirements for labeling fragrance allergens is crucial for businesses aiming to ensure compliance and safeguard consumer health. In this article, UCC will provide an overview of fragrance allergen labeling requirements, current regulations, and practical steps for businesses. […]
