What Colors to Avoid in Cosmetics & How to Label Them Correctly

In the beauty industry, the use of color additives is both a critical design element and a heavily regulated aspect. Color additives can enhance the appeal of cosmetics, making them more attractive and effective in meeting consumer expectations. However, the regulatory environment surrounding these additives is stringent, particularly when it comes to products intended for use around the sensitive area of the eyes. Ensuring compliance with FDA regulations is essential for the safety of consumers and the legality of cosmetic products.

Regulations and Approval

  • Approval and Certification: All color additives used in cosmetics must be approved by the FDA. This includes not only the approval of the substances themselves but also batch certification for many color additives to ensure they meet stringent safety and purity standards.

  • Specific Use Approval: Color additives are approved for specific uses, which means they can only be used in the manner outlined by the FDA. Any deviation from these approved uses results in the product being considered adulterated and illegal to sell.

The U.S. Food and Drug Administration (FDA) lists and regulates colors permitted for use in cosmetics under Parts 73-74, Subpart C of the FDA Regulation, specifically 21 C.F.R. §§ 73.2030-73.2995 and 74.2052-74.2711. These regulations are critical for cosmetic manufacturers to understand and follow diligently.

Specific Regulations for Eye-Area Cosmetics

The FDA strictly controls which color additives may be used in cosmetics intended for application in the area of the eye, one of the most sensitive regions where cosmetics are applied. For example:

  • Blue No. 1 (§74.2101)

  • Green No. 5 (§74.2205)

  • Red No. 40 (§74.2340)

  • Yellow No.5 (§74.2705)

These additives are explicitly noted in their respective regulations as safe for use in eye-area cosmetics. Additionally, the FDA specifies that you may not use a color additive in the area of the eye unless the regulation for that additive specifically permits such use [21 CFR 70.5(a)]. The "area of the eye" is defined comprehensively, including everything from the eyebrows to the eyelashes and the eyeball itself [21 CFR 70.3(s)].

Externally Applied Cosmetics

The term "externally applied cosmetics" does not extend to the lips or any body surface covered by mucous membrane. For instance, a color additive approved for use in externally applied cosmetics cannot be used in products such as lipsticks unless the regulation specifically permits this use [21 CFR 70.3(v)].

Non-Compliance with Color Additives Regulations

Under 21 C.F.R. § 70.5 (a), the listing or certification of a color additive does not automatically authorize its use in articles intended for use around the area of the eye unless such usage is specifically allowed in the color additive's certification. The FDA Color Additives Fact Sheet reinforces this rule, stating, "You may not use color additives in the area of the eye unless the regulation for that color additive specifically permits such use."

Any cosmetic product intended for use around the eyes that contains unapproved color additives is considered unsafe, misbranded, and adulterated under federal law. Furthermore, if such products are not properly labeled to caution consumers about their contents and intended use, the legal risks and the severity of non-compliance increase significantly.

Best Practices for Compliance

For cosmetic manufacturers and brands, ensuring compliance with FDA regulations on color additives is not just about legal adherence but also about consumer safety and brand integrity. Here are some best practices to consider:

  1. Thorough Ingredient Review: Regularly review all color additives used in cosmetics, especially those products intended for application around the eyes, lips, or any body surface covered by mucous membrane, to ensure they meet specific FDA guidelines.

  2. Accurate and Cautious Labeling: It is critical that all cosmetic labels not only reflect the contents accurately using the correct FDA-approved names for all color additives but also include appropriate cautionary statements where necessary. Labels should clearly inform consumers about the intended use of the product, particularly if it is designed for application around sensitive areas. Failure to provide this vital information can result in mislabeling, which can lead to severe legal consequences.

  3. Stay Informed: Keep abreast of any changes in FDA regulations regarding color additives. The FDA occasionally updates its policies and approvals based on new safety data.

  4. Seek Expert Guidance: When navigating the complexities of FDA regulations and cosmetic safety, consulting with specialized regulatory compliance attorneys is invaluable. These experts possess in-depth knowledge of the regulatory landscape and can offer strategic advice tailored to your specific needs. By partnering with professionals who specialize in FDA regulations, you can significantly reduce the risk of non-compliance, ensuring that both product formulation and marketing align with current legal standards.

Get in Touch

Marcha Isabelle Chaudry

Marcha Isabelle Chaudry, a distinguished attorney with over a decade of experience, is the founder of the Equity and Wellness Collaborative (EWC), a consultancy at the forefront of public and consumer policy and advocacy within the beauty, aesthetic, and wellness industries. Her expertise encompasses a deep understanding of regulatory compliance, strategic business solutions, and a commitment to promoting ethical practices and consumer safety.

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