Get Your Cosmetic Label Reviewed & Fixed — Instant Pricing
Book a cosmetic label compliance review and fix online. Compare vetted EU/UK/US compliance specialists with instant per-label pricing. Receive a corrected label, not just a report.
✓ 10 active providers available right now· USD 166 – 509
Why this page is different
Instant pricing: See a price estimate immediately (no back-and-forth RFQ needed for these services).
Compare before booking: Review inclusions, exclusions, turnaround, and communication channels.
Charged only when accepted: You are charged only after a provider accepts your order and scope.
Live availability: 10 active providers available right now for this service.
What you can compare here
Total price: See live price ranges and instant pricing rules where available.
Coverage & scope: Markets served, what is included, and what is explicitly excluded.
SLA & responsiveness: Acceptance SLAs and typical turnaround windows.
Add-ons: Optional extras you can book next (shown as add-on chips).
Onboarding time: How quickly providers can start and what you need to supply.
Compare providers (instant pricing + book)
Provider
Estimated base price
Accept SLA
Turnaround
Start
Northgate Regulatory Partners
USD 166
24h
3–5 days
Within 2 business days
Sterling Label & Compliance
USD 315
24h
3–5 days
Within 2 business days
Apex Medical Device Support
USD 509
24h
3–5 days
Within 2 business days
Belmont Regulatory Services
USD 315
24h
3–5 days
Within 2 business days
Summit Device Compliance
USD 509
24h
3–5 days
Within 2 business days
Estimates are derived from each provider’s published pricing rules (and may vary by your inputs).
What affects pricing
These are the inputs providers use to price your order. Enter them once, then compare providers and book instantly.
Upload your current label (PDF, DOCX, or AI/EPS) and select the markets you are selling into (EU, UK, US, or all three).
2
Compare reviewers with instant pricing
See per-label fees, turnaround, and what each provider delivers (report only vs. corrected label file).
3
Receive your compliant label
Your reviewer returns a marked-up report and/or a corrected label file ready for print production.
EU cosmetics labelling requirements under Regulation 1223/2009
Every cosmetic product sold in the EU must carry a label that complies with Article 19 of EU Cosmetics Regulation 1223/2009. Mandatory elements include: the name and address of the Responsible Person in the EU; the nominal content (weight or volume); the date of minimum durability ("best before") or Period After Opening (PAO) — typically a jar symbol with a number (e.g., 12M); special precautions for use; the product function or intended use (unless obvious from presentation); the batch number; and the full list of ingredients using INCI names in decreasing order of concentration, with the heading "Ingredients." For products with small packaging (below a certain size), some information may be provided on the outer packaging or in an enclosed leaflet, but INCI and warnings must always be on the product itself.
UK cosmetics labelling after Brexit
Since 1 January 2021, cosmetics sold in Great Britain must comply with the UK Cosmetics Regulation, which mirrors EU law with one key difference: the UK Responsible Person's address must be in Great Britain, not the EU. The INCI list, warnings, and PAO requirements are essentially identical. Northern Ireland continues to follow EU Cosmetics Regulation under the Windsor Framework. One practical consequence for brands: if you previously had a single pan-EU label with an EU RP address, you need a separate GB label (or label variant) showing a UK RP address for your Great Britain market stock. This is one of the most common compliance errors found in post-Brexit label reviews.
US cosmetic labelling requirements under 21 CFR Part 701
FDA cosmetic labelling requirements differ materially from EU/UK requirements. Under 21 CFR Part 701, required label elements include: identity of the product; name and place of business of the manufacturer/distributor; net quantity of contents; and directions for safe use where necessary. The ingredient declaration must appear under the heading "Ingredients" using PCPC INCI names in descending order of predominance. US labelling does not require a "Responsible Person" designation, nor a PAO symbol, and does not require a mandatory batch number on the label (though good practice). Under MoCRA, additional warning and labelling requirements may be introduced by FDA regulation — monitor FDA guidance for updates.
Common cosmetic label non-conformities found in reviews
The most frequent label failures identified in professional cosmetic label reviews include: incorrect INCI ingredient ordering (ingredients not in descending concentration order); INCI names that don't match the current CosIng database entries; missing allergen callouts required above the 0.001% threshold in EU (for leave-on products); missing or incorrect PAO symbol; Responsible Person address in the wrong jurisdiction (EU address on a UK-only product); claim language that implies a medicinal action and could trigger reclassification; missing mandatory warnings for products containing specific restricted substances; and missing dual-language requirements for products sold in officially bilingual jurisdictions.
Frequently asked questions
What does a cosmetic label compliance review cover?
A review checks your product name, INCI ingredient list (declaration order, nomenclature, allergen callouts), mandatory warnings, fill quantity, responsible person details, net quantity statement, and country-specific language requirements for your target market(s).
Do reviewers provide a corrected label or just a report?
It varies by provider. Some deliver only a non-conformity report; others return a corrected, production-ready label file. Filter by deliverable type when comparing.
Can you review labels for both EU and UK at the same time?
Yes. Many providers offer combined EU + UK reviews since the requirements diverged after Brexit but remain closely aligned. Expect a small upcharge for dual-market review.
My product formula changed — do I need a new review?
Yes. Any change to the ingredient list, concentrations, or function claims requires an updated compliance review before relabelling.
What file formats do reviewers accept?
Most reviewers accept PDF, DOCX, and image formats. Some also accept editable design files (AI, INDD). Confirm accepted formats with your chosen provider.
How Cruxi Bridge vets providers
✓ Every provider submits regulatory expertise evidence and jurisdictional coverage claims
✓ Providers that go live agree to the Cruxi Bridge Provider Terms including service delivery and accuracy obligations
✓ Payment is held by Cruxi and only released to the provider after service delivery milestones
✓ Buyers can raise a dispute within 30 days — Cruxi reviews and mediates per the platform terms
Prices and provider availability are live and may change. Charged only when a provider accepts your order.
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