Art. 23 Federal Act of 15 December 2000 on Medicinal Products and Medical Devices (TPA) - Categories of medicinal products
Legislator summary
AI generatedMedicinal products shall be classified into categories according to whether or not they are subject to prescription. A category of over-the-counter medicinal products shall be created for which neither medical and pharmaceutical nor professional customer advice is required. Articles 24–27 and 30 do not apply to this category. {note: Amended by No I of the FA of 18 March 2016, in force since 1 Jan. 2019 ( AS 2017 2745, 2018 3575; BBl 2013 1).} The Federal Council shall lay down the classification criteria. {note: Amended by No I of the FA of 18 March 2016, in force since 1 Jan. 2019 ( AS 2017 2745, 2018 3575; BBl 2013 1).}
Art. 23 TPA · Categories of medicinal products
Medicinal products shall be classified into categories according to whether or not they are subject to prescription.
A category of over-the-counter medicinal products shall be created for which neither medical and pharmaceutical nor professional customer advice is required. Articles 24–27 and 30 do not apply to this category.
The Federal Council shall lay down the classification criteria.