CPNP notification

Notification is required for all cosmetics intended for sale in the EU prior to their market launch. This is stipulated by Article 13 of EU Cosmetics Regulation 1223/2009.

Cosmetic products already registered in line with different countries’ systems in the past have to be resubmitted for notification.

How is notification handled?

The notification is sent electronically to the European Commission. The information about the cosmetic product including its formulation is made available to national poison control centres. In addition, information about a cosmetic product, aside from the formulation, is made available to the competent authorities for the purposes of monitoring products.

The EU has created a dedicated website, the Cosmetic Products Notification Portal (CPNP), which enables companies to submit product data and to continually keep this information up to date.

File downloads

What data must be submitted via the CPNP?

You should have the following data at hand when carrying out product notification using the Cosmetic Products Notification Portal:

  • The cosmetic product’s category and its name, enabling specific identification
  • The name and address of the responsible person where the product information file (PIF) is made accessible
  • The country of origin in case of import
  • The member state in which the cosmetic product is to be placed on the market
  • The contact details of a person to contact in the case of necessity
  • Nanomaterials, if necessary (with IUPAC name and exposure conditions)
  • Name and CAS or EC numbers of CMR substances
  • Frame formulation / detailed formulation
  • Original labelling and photo of the corresponding packaging

Nanomaterials: a special case

Cosmetics containing nanomaterials represent a special situation. These products require notification six months in advance of the product’s market launch. The existing Cosmetic Products Notification Portal (CPNP) was augmented for the purpose of supplying notification of nanomaterials. The database requires the following information:

  • Description and specification of the nanomaterial
  • Estimated quantity intended to be placed on the market per year
  • Toxicological profile
  • Safety data
  • Exposure conditions 

The only nanomaterial-containing cosmetics exempt from this more extensive form of notification are those used as colorants, UV filters or preservatives and which have received authorisation via the corresponding annexes to the cosmetics regulation. The European Commission’s objective is to ensure a high level of protection of human health. 



Contact us!
I agree to the privacy policy. I consent that reports related to products supported by Diapharm may be disclosed to a third party.

We are using cookies.

We use third party cookies for usage statistics and to further improve our website.