Get Form 17 See Rules 56 And 145-a Intimation To Person

The Drugs and Cosmetics Act, 1940 is an act of the Parliament of India which regulates the import, manufacture and distribution of drugs in India. The primary objective of the act is to ensure that the drugs and cosmetics sold in India are safe, effective and conform to state quality standards.

The United States Federal Food, Drug, and Cosmetic Act (abbreviated as FFDCA, FDCA, or FD&C) is a set of laws passed by the United States Congress in 1938 giving authority to the U.S. Food and Drug Administration (FDA) to oversee the safety of food, drugs, medical devices, and cosmetics.

The passage of the 1906 Pure Food and Drugs Act marked a monumental shift in the use of government powers to enhance consumer protection by requiring that foods and drugs bear truthful labeling statements and meet certain standards for purity and strength.

The Federal Food, Drug, and Cosmetic Act (FDCA) protects the public health and safety in a variety of ways. It forbids the manufacture or distribution of foods, drugs, medical devices, and cosmetics that are adulterated or misbranded.

Powers of Central Government to regulate, restrict or prohibit manufacture, etc., of drug and cosmetic in public interest. 26B. Powers of Central Government to regulate or restrict, manufacture, etc., of drug in public interest.

The Parliament of India formed an Act which regulates the import, manufacture and distribution of drugs in India. The primary objective of the Act is to ensure that the drugs and cosmetics sold in India are safe, effective and conform to prescribed quality standards.

The Drugs and Cosmetics Act restricts the import of: Drugs or cosmetics of substandard quality. Any misbranded or spurious cosmetic. Any adulterated or spurious drug. Any patent or proprietary medicine with no description of the formula or list of active ingredients included in it, along with the quantities thereof.