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Cosmetic Label Review Services

Cosmetic products distributed in the US must comply with FDA labeling regulations under the FD&C Act and the FPLA. LMG reviews your label, identifies non-compliances, and delivers a corrected, FDA-compliant version.
FD&C Act · FPLAIngredient NamingMoCRA 2022Since 2009
FDA cosmetic label review — non-compliant vs compliant label comparison under FD&C Act and FPLA
FD&C Act · FPLA
LMG reviews your cosmetic label against all applicable FDA requirements and delivers a corrected, market-ready compliant version.
FD&C Act+ FPLA
MoCRA2022
7–10 daysTurnaround
From $649LMG Fee

About FDA Cosmetic Label Compliance

Cosmetic products distributed in the US must comply with FDA labeling regulations under the FD&C Act and the FPLA. “Labeling” includes the product label and any written or graphic information accompanying the product.

Our regulatory team can assist you with compliance in the following areas:

  • Ingredient and color additive compliance
  • Cosmetic product name and identity
  • Marketing statements, claims, and taglines
  • General FDA cosmetic labeling requirements

Under the Modernization of Cosmetics Regulation Act (MoCRA) enacted in December 2022, cosmetic labeling requirements have become more stringent, with enhanced FDA enforcement authority and mandatory facility registration creating increased scrutiny of cosmetic product labels. Ensuring label compliance before market entry protects your brand from costly FDA warning letters, product recalls, and import detention while building consumer trust through transparent, accurate product information.

Liberty Management Group provides comprehensive cosmetic label review services to identify regulatory gaps and ensure full compliance with FDA requirements before your products reach consumers. Our regulatory specialists possess extensive knowledge of cosmetic ingredient nomenclature, prohibited and restricted ingredients, color additive certification requirements, and the evolving regulatory landscape following MoCRA implementation.

Frequently Asked Questions

Common questions about this FDA regulatory service.
It means the product’s labeling meets all applicable FDA requirements related to product identity, ingredient declaration, mandatory warnings, and formatting.
No. The FDA does not preapprove cosmetic labels. Manufacturers are fully responsible for ensuring compliance before marketing.

A compliant cosmetic label may include the following (this is not a complete list):

  • Product identity (what the product is)
  • Net quantity of contents
  • Manufacturer, packer, or distributor name and address
  • Ingredient list
  • Required warning statements
  • Proper label formatting and placement
Yes. Ingredients must follow the name designated by the Commissioner or names published in the most current edition of the CTFA/INCI.
Yes. Certain claims may cause a cosmetic to be classified as a drug, triggering additional regulatory requirements.
No. Registration and listing do not involve label approval. Compliance responsibility remains with the company.
Non-compliant labels may result in warning letters, import detention, product recalls, or import alerts.

Ready to Review Your Cosmetic Label?

Simply contact our regulatory team to guide you through the next steps.

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