
The Act on electronic cigarettes and refill containers for electronic cigarettes, No. 87/2018 harmonized the EU directive 2014/40 regulations on e-cigarettes and came into force on March 1, 2019.
E-cigarettes are classified as consumer products if they have lower content of nicotine than 20 mg/ml. Everything over 20 mg/ml is a medicinal product. E-cigarettes classified as medicinal products would require marketing authorization that must be obtained prior to marketing these products and they must meet all requirements on sale, advertising/promotion, distribution, manufacture, importation and marketing specified in the Medicines Act. Consumer based e-cigarettes will be subject to the European Union’s consumer product laws.
Medicines Act (http://www.webcitation.org/query?url=https%3A%2F%2Feng.velferdarraduneyt...)
Consumer products law (http://www.webcitation.org/query?url=http%3A%2F%2Fwww.webcitation.org%2F...)
Act on electronic cigarettes and refill containers for electronic cigarettes, No. 87/2018 (https://www.government.is/lisalib/getfile.aspx?itemid=37dbe67d-f4d4-11e9-9450-005056bc4d74)