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

20 marks

Speculated mark distribution:

part a) 3 marks, part b) 14 marks, part c) 3 marks