a) Define "medicine" under the Pharmacy and Poisons Ordinance.

b) Describe the labelling requirements for a medicine to be supplied in Hong Kong as stipulated under the Pharmacy and Poisons Ordinance and its Regulations. If the medicine is for export purpose, what labelling requirements apply?

c) What additional labelling requirements apply if the medicine (i) is a lotion; (ii) is for the treatment of an animal; (iii) contains a Part 1 Poison (except Schedule 3 Poison); and (iv) contains a Schedule 3 poison?