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US Label Review (Cosmetics)
Review of the package labeling to ensure compliance per US FDA regulations
Price per sample:
$100
Additional information
| Turnaround Time | 7 days |
|---|---|
| documents_required | PDF Artwork File |
| Sample Size | PDF Artwork File |
US Cosmetic Label Review
US cosmetic label review helps manufacturers confirm that product labels meet U.S. regulatory requirements before sale or distribution. At Pentyl Labs, we review cosmetic and personal care labels to support FDA compliance and reduce regulatory risk. This service helps brands move to market with greater confidence.
Because labeling errors can delay launches or trigger enforcement action, early review plays a critical role in product readiness. As a result, many companies treat label review as a standard step before release.
What Is Included in a US Cosmetic Label Review
During a US cosmetic label review, we examine required label elements under U.S. cosmetic regulations. We focus on clarity, accuracy, and consistency with current FDA expectations.
Our review typically includes:
-
Ingredient declarations using proper INCI names and order
-
Product identity statements
-
Net quantity of contents
-
Business name and place of business
-
Required warnings and caution statements
-
Claim language that may raise regulatory concerns
By reviewing labels as presented, we help identify issues that may require revision before printing or distribution.
When a Label Review Is Recommended
US cosmetic label review is recommended at several stages of the product lifecycle. For example, brands often request review:
-
Before a first U.S. product launch
-
After formulation or ingredient changes
-
When updating marketing or on-pack claims
-
For private label or contract-manufactured products
-
Prior to retailer or distributor submission
In addition, many companies use label review to document due diligence as part of broader compliance programs.
Regulatory Background
In the United States, the FDA regulates cosmetic labeling under the Federal Food, Drug, and Cosmetic Act. Label requirements appear in 21 CFR Parts 701 and 740 and are supported by FDA guidance documents.
Although cosmetics do not require premarket approval, labels must comply with applicable requirements at the time of sale. Therefore, manufacturers often reference FDA cosmetic labeling guidance when preparing or reviewing labels.
US Label Review Services at Pentyl Labs
At Pentyl Labs, we provide practical US cosmetic label review services with clear, actionable feedback. We focus on identifying potential risks while helping clients understand available options.
Ultimately, our goal is to support compliant labeling and smoother product launches. Many clients also combine label review with regulatory compliance testing or safety assessments to build complete documentation.
FDA cosmetic labeling requirements are published by the U.S. Food and Drug Administration. Cosmetics Labeling | FDA
Description
US Cosmetic Label Review
US cosmetic label review helps manufacturers confirm that product labels meet U.S. regulatory requirements before sale or distribution. At Pentyl Labs, we review cosmetic and personal care labels to support FDA compliance and reduce regulatory risk. This service helps brands move to market with greater confidence.
Because labeling errors can delay launches or trigger enforcement action, early review plays a critical role in product readiness. As a result, many companies treat label review as a standard step before release.
What Is Included in a US Cosmetic Label Review
During a US cosmetic label review, we examine required label elements under U.S. cosmetic regulations. We focus on clarity, accuracy, and consistency with current FDA expectations.
Our review typically includes:
-
Ingredient declarations using proper INCI names and order
-
Product identity statements
-
Net quantity of contents
-
Business name and place of business
-
Required warnings and caution statements
-
Claim language that may raise regulatory concerns
By reviewing labels as presented, we help identify issues that may require revision before printing or distribution.
When a Label Review Is Recommended
US cosmetic label review is recommended at several stages of the product lifecycle. For example, brands often request review:
-
Before a first U.S. product launch
-
After formulation or ingredient changes
-
When updating marketing or on-pack claims
-
For private label or contract-manufactured products
-
Prior to retailer or distributor submission
In addition, many companies use label review to document due diligence as part of broader compliance programs.
Regulatory Background
In the United States, the FDA regulates cosmetic labeling under the Federal Food, Drug, and Cosmetic Act. Label requirements appear in 21 CFR Parts 701 and 740 and are supported by FDA guidance documents.
Although cosmetics do not require premarket approval, labels must comply with applicable requirements at the time of sale. Therefore, manufacturers often reference FDA cosmetic labeling guidance when preparing or reviewing labels.
US Label Review Services at Pentyl Labs
At Pentyl Labs, we provide practical US cosmetic label review services with clear, actionable feedback. We focus on identifying potential risks while helping clients understand available options.
Ultimately, our goal is to support compliant labeling and smoother product launches. Many clients also combine label review with regulatory compliance testing or safety assessments to build complete documentation.
FDA cosmetic labeling requirements are published by the U.S. Food and Drug Administration. Cosmetics Labeling | FDA
