Translation of "Vente franco de port et d'emballage " (French → English) :

1. Food enzymes and food enzyme preparations not intended for sale to the final consumer, whether sold singly or mixed with each other, █may be marketed only where the packaging or containers bear the information provided for in this Article , which must be easily visible, clearly legible and indelible.

Without prejudice to Directive 2000/13/EC, food enzymes or food enzyme preparations intended for sale to the final consumer may be marketed only if their packaging contains the following information, which must be easily visible, clearly legible and indelible:

1. Without prejudice to Directive 2000/13/EC, Directive 89/396/EEC and, where appropriate, Regulation (EC) No 1829/2003, flavourings intended for sale to the final consumer may be marketed only if their packaging contains either the statement ║'for use in food" or the statement "restricted use in food" or a more specific reference to its intended food use, which must be easily visible, clearly legible and indelible.

1. The packaging or containers of flavourings not intended for sale to the final consumer shall bear the following information:

In the case of medicinal products that have been granted a marketing authorisation under Regulation (EC) No 726/2004, Member States may permit or require that the outer packaging bear additional information concerning distribution, possession, sale or any necessary precautions, provided that such information is not in infringement of Community law or the terms of the marketing authorisation, and is not promotional.

The Act provided for: a prohibition against importing or exporting drugs at a port not designated for that purpose by federal authorities; the issue of permits for the import, export, manufacture, sale and distribution of drugs; the imposition of criteria regarding packaging and labelling of packages containing such substances; an obligation for businesses to keep a record of their drug importing, exporting, manufacturing, sale and distribution activities duly authorized by federal authorities; an obligation for physicians to provide the information requested by federal authorities concerning the purchase, manufacture or prescription ...[+++] of medications containing drugs; an obligation for pharmacists to keep a record of their purchases and sales of drugs, the preparation of their own medications containing such substances and renewals of prescriptions signed by a physician; [58] and the authorization to sell medications (such as ointments and liniments) containing very small quantifies of scheduled drugs without a permit, provided they were not administered to children under two years of age and met certain labelling criteria.