a) Define ‘medicine’ per the PPO
b) Describe the labelling requirements for a medicine to be supplied in Hong Kong per the PPR. If the medicine is for export purposes what labelling requirements apply?
c) What additional labelling requirements apply if the medicine:
(i) is a liniment
(ii) contains a part 2 poison
(iii) contains a part 1 poison
Speculated mark distribution:
part a) 3 marks, part b) 14 marks, part c) 3 marks