Ordinance
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Art. 38 Labelling 185
1 The label must not be misleading in respect of the risks from the biocidal product to human health, animal health or the environment or its efficacy. It must not, in any case, mention the indications «low-risk biocidal product», «non-toxic», «harmless», «natural», «environmentally friendly», «animal friendly» or similar indications. 2 Biocidal products and active substances for use in biocidal products must be labelled:186
3 In addition to the details specified in paragraph 2, the following must be indicated on the label:189
4 Where applicable, the following must also be indicated:
5 Where this is necessary because of the size or the function of the biocidal product, the information specified in paragraph 3 letters c, e, f and i–l and paragraph 4 letter b must be indicated as follows:
6 ...193 185 Amended by No I of the O of 20 June 2014, in force since 15 July 2014 (AS 2014 2073). 186 Amended by No I of the O of 5 June 2015, in force since 1 July 2015 (AS 2015 1985). 187 [AS 2005 2721; 2007 821; 2009 401, 805; 2010 5223; 2011 5227; 2012 6103, 6659; 2013 201, 2673, 3041No I 3; 2014 2073Annex 11 No 1, 3857. AS 2015 1903Art. 91]. See now: the O of 5 June 2015 (SR 813.11). 188 Amended by No I of the O of 5 June 2015, in force since 1 July 2015 (AS 2015 1985). 189 Amended by No I of the O of 18 Nov. 2020, in force since 15 Dec. 2020 (AS 2020 5125). 190 Amended by No I of the O of 5 June 2015, in force since 1 July 2015 (AS 2015 1985). 191 Directive 2000/54/EC of the European Parliament and of the Council of 18 September 2000 on the protection of workers from risks related to exposure to biological agents at work, OJ L 262 of 17 October 2000, p. 21. 192 Amended by No I of the O of 18 Nov. 2020, in force since 15 Dec. 2020 (AS 2020 5125). 193 Repealed by No I of the O of 5 June 2015, with effect from 1 July 2015 (AS 2015 1985). |