Hazardous Products Act

This version of section 2 is in force from 2002-12-31 to 2011-06-19.

Marginal note:Definitions

 In this Act,

“advertise”

« publicité »

“advertise”, in relation to a prohibited product or restricted product, includes any representation by any means whatever for the purpose of promoting directly or indirectly the sale or other disposition of the product;

“analyst”

« analyste »

“analyst” means any person designated as an analyst under the Food and Drugs Act or pursuant to subsection 21(1);

“controlled product”

« produit contrôlé »

“controlled product” means any product, material or substance specified by the regulations made pursuant to paragraph 15(1)(a) to be included in any of the classes listed in Schedule II;

“hazardous product”

« produit dangereux »

“hazardous product” means any prohibited product, restricted product or controlled product;

“import”

« importer »

“import” means to import into Canada;

“inspector”

« inspecteur »

“inspector” means any person designated as an inspector pursuant to subsection 21(1);

“Minister”

« ministre »

“Minister” means the Minister of Health;

“prohibited product”

« produit interdit »

“prohibited product” means any product, material or substance included in Part I of Schedule I;

“restricted product”

« produit limité »

“restricted product” means any product, material or substance included in Part II of Schedule I;

“sell”

« vendre »

“sell” includes offer for sale, expose for sale and distribute.

  • R.S., 1985, c. H-3, s. 2;
  • R.S., 1985, c. 24 (3rd Supp.), s. 1;
  • 1992, c. 1, s. 145(F);
  • 1996, c. 8, s. 25.