The labelling of the medicinal products mentioned in II of article L. 5121-12-1 includes at least the following information:
1° The name of the medicinal product or, where appropriate, its code name or international non-proprietary name;
2° The name or business name and address of the company;
3° The batch number;
4° The route and, where appropriate, the method of administration of the medicinal product;
5° The expiry date;
6° Where applicable, the information required for proper storage of the medicinal product.