Contents:
The Drugs and Consmetics Act, 1940;
Chapter I. Introductory;
Chapter II. The Drugs Technical Advisory Board, The Central Drugs Laboratory and the Drugs Consultative Committee;
Chapter III. Import of Drugs and Cosmetics;
Chapter IV. Manufacture, Sale and Distribution of Drugs and Cosmetics;
Chapter IV-A. Provisions relating to ayurvedic, siddha and unani drugs;
Chapter V. Miscellaneous;

The Drugs and Consmetics Rules, 1945;
Part I-Preliminary;
Part II-The Central drugs laboratory;
Part III-
Part IV-Import and registration;
Part V-Government analysts, inspectors, licensing authorities and constrolling authorities;
Part VI-Sale of drugs other than homoeopathic medicines;
Part VI-A-Sale of homeopathic medicines;
Part VII-Manufactue for sale or for distribution of drugs other than homoepathic medicines;
Part VII-A-Manufacture for sale or for distribution of homoeopathic medicines;
Part VIII-Manufacture for examination, test or analysis;
Part IX-Labelling and packing of drugs other than homoepathic medicines;
Part IX-A-Labelling and packing of homoepathic medicines;
Part X-Special provisions relating to biological and other special products;
Part X-A-Import or manufacture of new drug for clinical trials or marketing;
Part X-B-Requirements for the collection, storage, processing and distribution of whole human blood, human blood components by blood banks and manufacture of blood products;
Part XI-Exeptions;
Part XII-Standards;
Part XIII-Import and registration of cosmetics;
Part XIV-Manufacture of consmetics for sale or for distribution;
Part XV-Labelling, packing and standards of cosmetics;
Part XV(A)-Approval of institutions for carrying out tests on drugs, cosmetics and raw materials used in their maufacture on behalf of licensees for manufactue for sale of drugs/cosmetics;
Part XVI-Manufacture for sale of ayurvedic (Including Siddha) or Unani drugs;
Part XVI-A-Approval of institutions for carrying out tests on ayurvedic, siddha and unani drugs and raw materials used in their manufacture on behalf of licensees for manufacture for sale of ayurvedic, siddha and unani drugs;
Part XVII-Labelling, packing and limit of alcohol in ayurvedic (including siddha) or unani drugs;
Part XVIII-Government analysts and inspectors for ayurvedic (including siddha) or unani drugs;
Part XIX-Standards of ayurvedic, siddha and unani drugs;;

The drugs (control) Act, 1950.