(a) Define "pharmaceutical product" under the Pharmacy and Poisons Ordinance. 

(3 marks) 

(b) Describe the registration requirements, exemptions, and factors relevant to determination of application for registration of pharmaceutical products as stipulated under the Pharmacy and Poisons Regulations. (12 marks) 

(c) Describe the labeling requirements with respect to pharmaceutical products for human parenteral administration containing sodium chloride 0.9% as active ingredient. (5 marks)