L 30/34 Official Journal of the European Union EN CN code 31.1.2019 Description ex 2924 29 98 3.4. Mixtures containing at least 0,3 % by weight of PAVA or OC and a solvent (such as ethanol, 1-propanol or hexane), which could be administered as such as incapacitating or irritating agents, ex 2939 99 00 in particular in aerosols and in liquid form, or used for manufacturing of incapacitating or irri­ tating agents ex 3301 90 30 ex 3302 10 90 Notes: ex 3302 90 10 1. This item does not control sauces and preparations therefor, soups or preparations therefor and mixed condiments or seasonings, provided that PAVA or OC is not the only constituent flavour in ex 3302 90 90 them ex 3824 90 97 2. This item does not control medicinal products for which a marketing authorisation has been granted in accordance with Union law (2) ex 8424 20 00 3.5. Fixed equipment for the dissemination of incapacitating or irritating chemical substances, which can be attached to a wall or to a ceiling inside a building, comprises a canister of irritating or in­ ex 8424 89 00 capacitating chemical agents and is activated using a remote control system Note: In addition to relevant chemical substances, such as riot control agents or PAVA, the goods controlled by items 3.3 and 3.4 shall be deemed to be incapacitating or irritating chemical substances ex 8424 20 00 3.6. Fixed or mountable equipment for the dissemination of incapacitating or irritating chemical agents that covers a wide area and is not designed to be attached to a wall or to a ceiling inside ex 8424 89 00 a building ex 9304 00 00 Notes: 1. This item does not control equipment controlled by item ML7(e) of the Common Military List of the European Union 2. This item also controls water cannons 3. In addition to relevant chemical substances, such as riot control agents or PAVA, the goods con­ trolled by items 3.3 and 3.4 shall be deemed to be incapacitating or irritating chemical substances (2) See in particular Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency (OJ L 136, 30.4.2004, p. 1) and Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use (OJ L 311, 28.11.2001, p. 67).