US FDA Cosmetic Labeling Guidelines

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US FDA Cosmetic Labeling Guidelines

Allergic reactions are a common issue that can be caused by exposure to or consumption of allergens, with symptoms ranging from mild rashes to life-threatening anaphylactic shock.

At present, there are extensive labeling guidelines in the food and beverage industry to protect consumers. However, the use of cosmetics may also cause allergic reactions, so it is crucial for consumer safety to establish labeling requirements for cosmetics. Therefore, the FDA is strictly enforcing cosmetic labeling regulations.

According to the Cosmetic Modernization Act (MoCRA), the FDA is strictly implementing cosmetic labeling regulations, particularly regarding the labeling requirements for allergens in cosmetics.

Therefore, cosmetic companies need to update product labels to comply with the new MoCRA cosmetic labeling requirements. Timely understanding of eFDA cosmtic labeling requirements is crucial for businesses.

FDA Cosmetic Allergen List

The FDA has identified five types of allergens that cause most cosmetic allergic reactions: metals, preservatives, dyes, fragrances, and natural rubber.

MoCRA Regulations: Changes to FDA Cosmetic Labeling Guidelines

The new MoCRA aims to strengthen the regulatory guidelines for cosmetics and protect consumer health. It has issued additional regulatory requirements for the sale of cosmetics in the United States. According to the MoCRA guidelines, cosmetic companies will be required to submit a declaration for each cosmetic product, including ingredient information and applicable warnings.

These changes aim to improve transparency and consumer safety. Therefore, manufacturers of cosmetics containing potential spice allergens will need to list spice allergens on product labels.

Understanding the New FDA Cosmetic Labeling Guidelines: MoCRA Requirements

MoCRA has introduced new labeling requirements for cosmetic products. Therefore, compliance with the new FDA cosmetic labeling guidelines is mandatory for cosmetic manufacturers. The product label should include the correct declared product identification and net content. In addition, it should include a correctly declared list of ingredients, company name and address, country of origin, and any necessary warnings/precautions. Incorrect labels may be considered as product mislabeling.In addition to label content, the guidelines also specify label placement, font size, and saliency.

New FDA Cosmetic Labeling Guidelines: Key Points to Remember

We emphasized some key points to remember when labeling cosmetic products:

1. The product label should be large enough to clearly display the required information in easy to read font.

2. The product ingredients should be listed in descending order of weight, using the most commonly used industry standard names.

3. Products that require warnings and/or safety instructions must be presented in a clear and prominent manner.

If there are multiple tags, the basic necessary information should appear on the main display panel.

5. The FDA does not define or regulate terms such as “natural” or “organic,” but your product should not be mislabeled or mislabeled.

6. The necessary label content includes product name, net content, safety instructions, any warnings or precautions, ingredient list, and company information.

If you need to learn more about FDA’s requirements for cosmetics, BTF provides a one-stop solution for cosmetics to ensure that your products are marketed in accordance with regulations to meet regulatory requirements.

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Post time: Dec-06-2024