Cosmetic product labeling is an area supported by the REJIMUS team, inclusive of formulation reviews, cosmetic manufacturer selection and facility audits, and support for ensuring packaging integrity. Additionally, the team is well versed in providing support for US importation and the evaluation of foreign market regulations to support exports.
Subpart A – General Provisions
§ 701.1 – Misbranding.
§ 701.2 – Form of stating labeling requirements.
§ 701.3 – Designation of ingredients.
§ 701.9 – Exemptions from labeling requirements.
Subpart B – Package Form
§ 701.10 – Principal display panel.
§ 701.11 – Identity labeling.
§ 701.12 – Name and place of business of manufacturer, packer, or distributor.
§ 701.13 – Declaration of net quantity of contents.
Subpart C – Labeling of Specific Ingredients
§ 701.20 – Detergent substances, other than soap, intended for use in cleansing the body.
§ 701.30 – Ingredient names established for cosmetic ingredient labeling.
All information on this page is current as of September 12, 2022.
Navigating the complexities of FDA regulations requires a deep understanding of cosmetic labeling standards set forth in 21 CFR Part 701. REJIMUS assists brands in meticulously reviewing their product labels to prevent costly misbranding issues and ensure all mandatory statements are properly displayed.
From establishing accurate principal display panels to correctly listing the name and place of business for manufacturers, packers, or distributors, our regulatory experts provide end-to-end support. By aligning your packaging with federal guidelines, you mitigate import risks and build greater consumer trust in the US market.