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The Drugs and Cosmetics Rules, 1945 has provisions for classification of drugs under given schedules and there are guidelines for the storage, sale, display and prescription of each schedule. [1] The Rule 67 details the conditions of licenses. The Rule 97 contains the labeling regulations. [3] The notable Schedules include:
Schedule X is a class of prescription drugs in India appearing as an appendix to the Drugs and Cosmetics Rules introduced in 1945. These are drugs which cannot be purchased over the counter without a valid prescription of a Registered Medical Practitioner (RMP). Also, the retailer has to preserve the prescription for a period of two years. [1]
The Schedule J of the Drugs and Cosmetics Rules, 1945 of India contains "a list of diseases and ailments which a drug may not claim to prevent or cure".Under Rule 106 of the Drugs and Cosmetics Act, 1940, a drug cannot make claims to treat or prevent any of the diseases or reform the conditions listed.
Download QR code; Print/export Download as PDF; ... Drugs and Cosmetics Rules, 1945; E. EC Regulation 1223/2009 on cosmetics; F. Federal Food, Drug, and Cosmetic Act ...
Schedule H is a class of prescription drugs in India appearing as an appendix to the Drugs and Cosmetics Rules, 1945 introduced in 1945. These are drugs which cannot be purchased over the counter without the prescription of a qualified doctor. The manufacture and sales of all drugs are covered under the Drugs and Cosmetics Act and Rules.
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. [1] 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. [ 2 ]
Drugs and Cosmetics Act: 1940: 23 Coffee Act: 1942: 7 Reciprocity Act: 1943: 9 Central Excise Act: 1944: 1 Public Debt Act: 1944: 18 International Monetary Fund and Bank Act: 1945: 0 Industrial Employment (Standing Orders) Act: 1946: 20 Delhi Special Police Establishment Act: 1946: 25 Foreigners Act: 1946: 31 Industrial Disputes Act: 1947: 14 ...
Title 21 is the portion of the Code of Federal Regulations that governs food and drugs within the United States for the Food and Drug Administration (FDA), the Drug Enforcement Administration (DEA), and the Office of National Drug Control Policy (ONDCP). [1] It is divided into three chapters: Chapter I — Food and Drug Administration