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That proportion shall be increased to 32 % for Member States with two official languages and 35 % for Member States with more than two official languages. The Commission shall be empowered to adopt delegated acts in accordance with Article 27 to adapt the wording of the health warning laid down in paragraph 1 to scientific developments. The labelling of unit packets and any outside packaging and the tobacco product itself shall not include any element or feature that: (a) promotes a tobacco product or encourages its consumption by creating an erroneous impression about its characteristics, health effects, risks or emissions; labels shall not include any information about the nicotine, tar or carbon monoxide content of the tobacco product; (b) suggests that a particular tobacco product is less harmful than others or aims to reduce the effect of some harmful components of smoke or has vitalising, energetic, healing, rejuvenating, natural, organic properties or has other health or lifestyle benefits; (c) refers to taste, smell, any flavourings or other additives or the absence thereof; (d) resembles a food or a cosmetic product; (e) suggests that a certain tobacco product has improved biodegradability or other environmental advantages. The unit packets and any outside packaging shall not suggest economic advantages by including printed vouchers, offering discounts, free distribution, two-for-one or other similar offers. The elements and features that are prohibited pursuant to paragraphs 1 and 2 may include but are not limited to texts, symbols, names, trademarks, figurative or other signs.Tobacco for oral use Member States shall prohibit the placing on the market of tobacco for oral use, without prejudice to Article 151 of the Act of Accession of Austria, Finland and Sweden. Member States may prohibit cross-border distance sales of tobacco products to consumers.Member States shall cooperate to prevent such sales.Retail outlets engaging in cross-border distance sales of tobacco products may not supply such products to consumers in Member States where such sales have been prohibited.Member States which do not prohibit such sales shall require retail outlets intending to engage in cross-border distance sales to consumers located in the Union to register with the competent authorities in the Member State, where the retail outlet is established, and in the Member State, where the actual or potential consumers are located.Retail outlets established outside the Union shall be required to register with the competent authorities in the Member State where the actual or potential consumers are located. Process for adapting the wording of health warnings 13. Member States may charge manufacturers and importers proportionate fees for receiving, storing, handling and analysing the information submitted to them. Member States shall ensure that: (a) nicotine-containing liquid is only placed on the market in dedicated refill containers not exceeding a volume of 10 ml, in disposable electronic cigarettes or in single use cartridges and that the cartridges or tanks do not exceed a volume of 2 ml; (b) the nicotine-containing liquid does not contain nicotine in excess of 20 mg/ml; (c) the nicotine-containing liquid does not contain additives listed in (d) only ingredients of high purity are used in the manufacture of the nicotine-containing liquid. Basis for controlling products that present a serious risk to health 12. Where Member States consider that the information submitted is incomplete, they shall be entitled to request the completion of the information concerned.

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The notification shall be submitted in electronic form six months before the intended placing on the market.All retail outlets intending to engage in cross-border distance sales shall submit at least the following information to the competent authorities when registering: 2.The competent authorities of the Member States shall ensure that consumers have access to the list of all retail outlets registered with them.The Commission shall determine, as soon as possible after having received that information, whether the provisional measure is justified.The Commission shall inform the Member State concerned of its conclusions to enable the Member State to take appropriate follow-up measures.