Part,  Chapter, Paragraph

1   II,     5. 10.  5|        a provisional labelling exemption for these ingredients or
2   II,     5. 10.  5| substances for which temporary exemption was granted, that were submitted
3  III,    10.  4.  2| subsequent recipient, with the exemption of retailers to final consumers.~ ~
4   IV,    11.  6.  2|         This can be done using exemption mechanisms. The role of
5   IV,    13.  7.  5| monitoring, the first relevant exemption is explicit consent from
6   IV,    13.  7.  5|    paragraph 2(a)). The second exemption is given in paragraph 3:
7  Key,   Ap5.  0.  0|    eur-b1~eur-c~eutrophication~exemption~exemptions~exercise~exotoxin~