TITLE V

LABELLING AND PACKAGE LEAFLET
Article 65
In consultation with the Member States and the parties concerned, the Commission shall draw up and publish detailed guidance concerning in particular:
1. the wording of certain special warnings for certain categories of medicinal products;
2. the particular information needs relating to non-prescription medicinal products;
3. the legibility of particulars on the labelling and package leaflet;
4. the methods for the identification and authentication of medicinal products;
5. the list of excipients which must feature on the labelling of medicinal products and the way in which these excipients must be indicated;
6. harmonised provisions for the implementation of Article 57.
Substituted by Directive 2004/27/EC of the European Parliament and of the Council of 31 March 2004 amending Directive 2001/83/EC on the Community code relating to medicinal products for human use.