As used in this chapter, the singular includes the plural and the masculine includes the feminine and neuter genders. The following terms, as used in this chapter, have the following meanings:
(a) “Person” means a natural person, individual, partnership, corporation, trust, estate, incorporated or unincorporated association, and any other legal or commercial entity however organized.
(b) “Personal Use” means the sale of below-threshold quantities in a single transaction is six (6) grams of ephedrine or ephedrine product pseudoephedrine or pseudoephedrine product, or phenylpropanolamine or phenypropanolamine products, or more than nine (9) grams of ephedrine or ephedrine product, or pseudoephedrine or pseudoephedrine product, or phenylpropanolamine or phenylpropanolamine products within any 30-day period.
(c) “Behind the counter” means shall be stored in a manner as to be directly accessible to the pharmacist, manager or store employee only. No customers shall be able to reach or access ephedrine or ephedrine products, pseudoephedrine or pseudoephedrine products, or phenylpropanolamine or phenylpropanolamine products without assistance from the staff employed at the store or pharmacy.
(d) “Ephedrine” means any material, compound mixture, or preparation that contains any quantity of ephedrine, its salts or optimal isomers, or salts of optimal isomers.
(e) “Ephedrine Products” means any consumer product that consists of a single- ingredient preparation of ephedrine in which ephedrine is the single active ingredient except if it is in pediatric form, or in liquid, liquid capsule or gel capsule form.
(f) “Pseudoephedrine” means any material, compound, mixture, or preparation that contains any quantity of pseudoephedrine, its salts or optimal isomers, or salts of optional isomers.
(g) “Pseudoephedrine product” means any consumer product that consists of a single-ingredient preparation of pseudoephedrine in which pseudoephedrine is the single active ingredient except if it is in pediatric form, or in liquid, liquid capsule or gel capsule form.
(h) “Phenylpropanolamine” means any material, compound, mixture, or preparation that contains any quantity of phenylpropanolamine, its salts or optimal isomers, or salts of optimal isomers.
(i) “Phenylpropanolamine product” mean any consumer product that consists of a single-ingredient preparation of phenylpropanolamine in which phenylpropanolamine is the single active ingredient except if it is in pediatric form, or in liquid capsule or gel capsule form.
(Ord. 125-2005. Passed 12-6-05.)