Food and Drug Administration Revises Cosmetic External Packaging Standards - Clarifying 4 Types: Capsule, Refill, etc.

Clarification of Cosmetic External Packaging Labeling Standards…Clear Methods for Capsule and Refill Products

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Clarification of Cosmetic External Packaging Labeling Standards…Clear Methods for Capsule and Refill Products

FDA Revises Q&A Compilation…Updating Gift Set and Small Container Labeling Cases

The Food and Drug Administration has revised the 'Q&A Compilation on Cosmetic External Packaging Labeling and Display.' This is a measure to reduce confusion in the industry regarding cosmetic external packaging labeling by clearly outlining methods for labeling capsule, refill products, small containers, and gift sets, which are increasingly prevalent in the market. This revision is expected to significantly contribute to helping the industry comply with regulations and enhancing consumers' right to know.

Why Update Cosmetic Labeling Standards Now?

This revision of the Q&A compilation is a follow-up to the policy enforced in February last year, which mandated listing key information on the outer surface of cosmetic containers and packaging. It is designed to help cosmetic marketers clearly implement the system on the ground, with significant contributions from the 'Jump-up K-Cosmetic Council' discussions. This can be interpreted as part of efforts to increase the effectiveness of regulations in response to rapidly changing market environments and the launch of various new types of products.

Examining the Core Content of the Revised Q&A Compilation

This revised Q&A compilation reflects the demands of the rapidly changing cosmetics market by clarifying the previously somewhat ambiguous labeling standards to minimize industry confusion and increase consumers' accessibility to information.

Clear Labeling of Capsule Packaged Products: Individually Packaged Items

The revised Q&A includes detailed methods for labeling the external packaging of individually packaged single-use products like capsule packaging. This provides practical guidelines considering the characteristics of the products, helping both manufacturers and consumers easily grasp and understand product information.

Small Containers and Refill Products: Guidelines with Enhanced Practicality

In particular, the external packaging labeling cases for cosmetics that were difficult to list all essential information due to small containers have been updated. Practical solutions are presented to efficiently utilize limited labeling space while delivering crucial information to consumers. Additionally, methods for listing labeling information on refill containers, which are gaining popularity in line with environmental protection and sustainable consumption trends, are clearly outlined, expected to positively impact the expansion of the refill market and strengthen consumer choice.

Gift Set: Integrated Information at a Glance

The labeling methods for cosmetic gift sets have also been clarified in this revision. In cases where multiple products are sold together as a gift set, clear standards for displaying individual product information and overall set information were necessary. The revision allows consumers to more easily access essential information such as full ingredients and usage methods when purchasing gift sets, aiding smart purchasing decisions.

Providing Transparent Information for Consumers

Jun-Su Shin, Director General of the Bio and Herbal Bureau of the Food and Drug Administration, expressed expectations that this revision of the Q&A compilation would be a practical help for consumers to meticulously check full ingredient lists and select products.

He emphasized the continuous strengthening of communication centered in the field to additionally rationalize the operation of the cosmetic system. This reflects the firm determination of the FDA to prioritize consumers' safety and right to information.

The revised Q&A compilation is easily accessible on the Food and Drug Administration's website. Industry representatives can thoroughly understand and comply with the changed regulations, while consumers can engage in more transparent informed consumption.

Positive Ripple Effects Expected from the Change

The FDA's revision of the Q&A compilation reflects the rapidly changing cosmetics market trends and the effort to create a rational regulatory environment benefiting both consumers and the industry. Clear labeling standards for various product types like capsule, refill, small containers, and gift sets will reduce industry confusion and significantly enhance consumers' access to information. We expect this to be a continuing system contributing to the healthy growth of the K-beauty industry and securing consumer trust through ongoing in-field communication.


Understanding the changing cosmetic labeling regulations and communicating trust to consumers is very important. supports brand growth by providing practical blog marketing solutions to ensure such core information is conveyed transparently and effectively.

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