Cosmetic Labeling Compliance Review Services
EasyComply reviews the actual artwork and claims against the selected market and product facts, then returns a traceable issue list and revision actions. The service is a review, not authority approval.
What This Service Does
This service checks a cosmetic label and its marketed claims for a defined product and target market. The output separates confirmed issues, questions that need product evidence and market-specific revision actions.
Review Scope
- Product identity, intended use and cosmetic-versus-drug boundary.
- Principal display and information panels.
- Responsible business or responsible-person details.
- Net contents, origin, durability, batch and warning statements where applicable.
- Ingredient declaration and market-specific naming or language needs.
- Claims, directions and supporting evidence supplied by the client.
- Artwork consistency across container, packaging and inserts.
Market Boundaries
EU cosmetic labels are governed by Article 19 of Regulation (EC) No 1223/2009 and related product-specific requirements. [20]
FDA labeling material must be read with the FD&C Act and Fair Packaging and Labeling Act for the actual U.S. product and claims. [15]
Great Britain and Canada have their own official labeling frameworks; an EU or U.S. review is not automatically reusable in either market. [UK-COSMETICS-GUIDE][CA-COSMETICS-LABEL]
What You Receive
- A dated review scope and product-version record.
- An annotated issue register grouped by severity and market.
- Official source links and locators for regulatory issues.
- Revision actions for artwork, copy or missing evidence.
- A list of unresolved product facts that prevent a conclusion.
- A final review pass for the revised version included in the agreed scope.
What We Need From You
- Target market and planned sales channel.
- Current container, outer-pack and insert artwork.
- Formula or ingredient declaration and product form.
- Exact claims, directions and warnings.
- Responsible business details and country of manufacture.
- Available claim, safety and test evidence.
Start a Review
Send the target market, product type and current artwork through the consultation form. EasyComply will first confirm the review scope and the evidence needed before work begins.
Official Sources
| # | Authority | Document | Locator | Published / Effective | Link |
|---|---|---|---|---|---|
| 1 | European Parliament and Council | Regulation (EC) No 1223/2009 on cosmetic products | Articles 3–5, 8, 10–13, 19–20, 23 and applicable Annexes | 2026-05-01 / 2013-07-11 | Official source |
| 2 | U.S. Food and Drug Administration | Cosmetics Labeling Guide | General labeling requirements | — / — | Official source |
| 3 | UK Office for Product Safety and Standards | Making cosmetic products available to consumers in Great Britain | Responsible Person, PIF, CPSR, labelling and notification sections | 2021-10-04 / — | Official source |
| 4 | Health Canada | Labelling of Cosmetics | Cosmetics labelling framework and consumer information requirements | — / — | Official source |
Disclaimer
This article is for general information and does not constitute legal or regulatory advice. Check the official source and your product facts before making a market decision.
posts
Entering the EU Cosmetics Market: A Practical Compliance Guide
Use the EU regulation as the starting point, then turn each obligation into an evidence-backed work item.
US Cosmetics Compliance Guide
Separate federal legal requirements from internal recommendations before assigning work to a product team.