European Union · Cosmetics
EU Cosmetic Nanomaterials Reporting
A practical guide to EU Cosmetic Nanomaterials Reporting for cosmetics sold in the European Union: who it applies to, what to prepare, and the mistakes that cause rejection.
Who needs this
- Brands and importers placing cosmetics on the market in the European Union
- Online sellers listing cosmetics for buyers in the European Union
Documents you need
- Product information file with a safety assessment
- GMP certificate for the manufacturing site
- Ingredient and labelling compliance review
- Local notification, registration, or acknowledgement
Compliance checklist
Tick each item as you collect it. Saved in this browser only.
How to comply
- Confirm the product is legally a cosmetic in this market
- Compile the product information file and safety assessment
- Complete the local notification or registration step
- Check labels, warnings, and claims against local rules
Brief for your lab or agent
Copy this into an email, then edit the product and channel.
Request: EU Cosmetic Nanomaterials Reporting — European Union Product category: Cosmetics Authority: European Commission Legal basis: Regulation (EC) 1223/2009 article 16 Documents we already have: 1. Product information file with a safety assessment 2. GMP certificate for the manufacturing site 3. Ingredient and labelling compliance review 4. Local notification, registration, or acknowledgement Questions: 1. Does our product fall under EU Cosmetic Nanomaterials Reporting in the European Union? 2. Which test standards or evidence do you accept? 3. What is the current fee and lead time? 4. Is a local representative required, and can you act as one?
Cost and timeline
Before sale; notification review typically takes weeks.
Official fees are usually low; testing and local representation add cost.
Common rejection reasons
- Missing or incomplete product information file
- Claims that are not supported by evidence
- Label not in a required local language
- Manufacturer GMP certificate missing or expired
Official sources
FAQ
Who needs EU Cosmetic Nanomaterials Reporting in the European Union?
Brands and importers placing cosmetics on the market in the European Union. Online sellers listing cosmetics for buyers in the European Union. The importer of record normally holds the evidence.
What documents do I need for EU Cosmetic Nanomaterials Reporting?
Product information file with a safety assessment; GMP certificate for the manufacturing site; Ingredient and labelling compliance review; and local notification, registration, or acknowledgement.
What is the first step for EU Cosmetic Nanomaterials Reporting?
Confirm the product is legally a cosmetic in this market, then compile the product information file and safety assessment. Before sale; notification review typically takes weeks.
How long does EU Cosmetic Nanomaterials Reporting take?
Before sale; notification review typically takes weeks.
How much does EU Cosmetic Nanomaterials Reporting cost?
Official fees are usually low; testing and local representation add cost.
What happens if I sell without it?
Recall, import block, fines, or marketplace delisting.
Who regulates EU Cosmetic Nanomaterials Reporting in the European Union?
European Commission.
Related requirements
Need this checked before launch?
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