Cosmetic Labelling Review

The cosmetics’ labels you use in non-EU countries are very likely not ready to be used in the European Union. Your Responsible Person (RP) makes sure that your labels meet the EU requirements, including all information and details that the law requires.

Let’s talk, we will be happy to offer you a free consultation on your cosmetic labels!

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As your professional Responsible Person,

The labelling of a cosmetic includes inner labels, outer labels, and leaflet. Overall, the final artwork of a cosmetic product labelling, must contain the following information:

  • Full commercial name of your cosmetic product
  • Product function (When the precautions for use cannot appear on the container and outer packaging for practical reasons, they can be added to an insert/leaflet. In this case the “open book” symbol shall appear on the labelling)
  • Particular precautions for use (when the precautions for use cannot appear on the container and outer packaging for practical reasons, they can be added to an insert/leaflet. In this case the “open book” symbol shall appear on the labelling)
  • Ingredient list (ingredients shall be listed with their INCI names in descending order of concentration. The ingredients list may appear on the outer packaging only)
  • Expiry date (date of minimum durability or PAO. (Period after opening) for products which durability is more than 30 months)
  • Responsible Person name and address
  • Manufacturer’s name and address (recommended)
  • Batch number (when impossible, for practical reasons, to make it appear on the product container, it may appear only on the outer packaging)
  • Product country of origin (“Made in … “ only if manufactured outside the European Union)
  • Nominal quantity (the nominal content at the time of packaging, given by weight or by volume, except for packaging containing less than 5 grams or milliliters, free samples and single‐application packs).

*This label example is only for general information and cannot be applied automatically to any product.

In the European Union, cosmetic claims must meet certain criteria and do not over-promise, exaggerate, or include statements that are not considered cosmetic claims (e.g., medical claims).

Our experts will:

  • review wording
  • help you rephrase
  • collect proof of claims

Compliance Success Stories

Why Obelis?

Our deep and long-standing experience with Swiss, EU and UK compliance frameworks makes us the best choice to support your products’ path towards compliance in these territories.

Our team regulatory experts will guide you through medical devices’ technical documentation, notification, labelling, among others.

About us
Founded in 1988, we are among Europe’s largest centres for advisory and representative services.
We are certified by ISO 9001:2015 and ISO 13485:2016.
We have helped over 3,000 manufacturers from over 60 countries address their regulatory challenges.
We are members of professional associations and more than 10 European Commission working groups.
Obelis International Offices (OIO) comprise independent partners providing solutions in other global markets.
Our team consists of lawyers, chemists, pharmacists, and other experts. Our close-knit culture has been certified by the Great Place to Work Survey 2022-23.