Ordinance
on the Placing on the Market and Handling of Biocidal Products
(Ordinance on Biocidal Products, OBP)


Open article in different language:  DE  |  FR  |  IT
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

a.
in ac­cord­ance with the sum­mary of the biocid­al product char­ac­ter­ist­ics re­ferred to in Art­icle 20 para­graph 2 let­ter b; and
b.
in ac­cord­ance with Art­icles 10 and 93 para­graph 1 let­ter b of the ChemO187 mu­tatis mutandis; where the ChemO refers:188
1.
to the man­u­fac­turer, this shall be un­der­stood for the pur­poses of this Or­din­ance as the au­thor­isa­tion hold­er,
2.
to dan­ger­ous sub­stances and pre­par­a­tions, this shall be un­der­stood for the pur­poses of this Or­din­ance as all biocid­al products and act­ive sub­stances for use in biocid­al products.

3 In ad­di­tion to the de­tails spe­cified in para­graph 2, the fol­low­ing must be in­dic­ated on the la­bel:189

a.
the iden­tity of every act­ive sub­stance and its con­cen­tra­tion in met­ric units;
b.
the Swiss au­thor­isa­tion num­ber;
c.190
the type of for­mu­la­tion;
d.
the uses for which the biocid­al product is au­thor­ised;
e.
dir­ec­tions for use; in par­tic­u­lar, for each use provided for un­der the terms of the rul­ing, the fol­low­ing are to be spe­cified:
1.
the fre­quency of ap­plic­a­tion,
2.
the dose rate, ex­pressed in met­ric units, in a man­ner which is mean­ing­ful and com­pre­hens­ible to the user;
f.
par­tic­u­lars of likely dir­ect or in­dir­ect ad­verse side ef­fects and any dir­ec­tions for first aid;
g.
the nan­o­ma­ter­i­als con­tained in the product, if any, and any spe­cif­ic re­lated risks, and, fol­low­ing each ref­er­ence to nan­o­ma­ter­i­als, the word «nano» in brack­ets;
h.
if ac­com­pan­ied by a leaf­let: the sen­tence «Read at­tached in­struc­tions be­fore use» and, where ap­plic­able, warn­ings for vul­ner­able groups;
i.
dir­ec­tions for the safe dis­pos­al of the biocid­al product and its pack­aging, in­clud­ing, where rel­ev­ant, any pro­hib­i­tion on the re­use of pack­aging;
j.
the for­mu­la­tion batch num­ber or des­ig­na­tion;
k.
the ex­piry date rel­ev­ant to nor­mal con­di­tions of stor­age;
l.
where ap­plic­able, the fol­low­ing de­tails:
1.
the time to on­set of the biocid­al ef­fect,
2.
the in­ter­val to be ob­served between ap­plic­a­tions of the biocid­al product,
3.
the in­ter­val to be ob­served between ap­plic­a­tion and the next use of the product treated, or the next ac­cess by hu­mans or an­im­als to the area where the biocid­al product has been used, in­clud­ing par­tic­u­lars con­cern­ing:
de­con­tam­in­a­tion means and meas­ures and dur­a­tion of ne­ces­sary vent­il­a­tion of treated areas
ad­equate clean­ing of equip­ment
pre­cau­tion­ary meas­ures dur­ing use and trans­port.

4 Where ap­plic­able, the fol­low­ing must also be in­dic­ated:

a.
the cat­egor­ies of users;
b.
in­form­a­tion on any spe­cif­ic danger to the en­vir­on­ment, par­tic­u­larly con­cern­ing pro­tec­tion of non-tar­get or­gan­isms and avoid­ance of con­tam­in­a­tion of wa­ter;
c.
for biocid­al products con­sist­ing of or con­tain­ing mi­croor­gan­isms: la­belling re­quire­ments in ac­cord­ance with Dir­ect­ive 2000/54/EC191.

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:

a.
on the pack­aging; or
b.
in an ac­com­pa­ny­ing leaf­let con­tained in the pack­aging.192

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).

Diese Seite ist durch reCAPTCHA geschützt und die Google Datenschutzrichtlinie und Nutzungsbedingungen gelten.

Feedback
Laden