Identification of raw materials

In force Act 23 of 1940 As on 15 Oct 2026

Read from the scanned gazette. India Code publishes no text for this Act, so the text below was read from the Government's own scan by machine and split into sections by its numbering. It has not been checked against the page word by word. Where it matters, read the scan. Read the scan.

Act 23 of 1940

Read from the scanned gazette. India Code publishes no text for this Act, so this text was read from the Government's own scan by machine and split into sections by its numbering. It has not been checked against the page word by word. Where it matters, read the scan. Read the scan.

Section 160 of the Drugs and Cosmetics Act and Rules deals with identification of raw materials. Raw materials used in the preparation of Ayurvedic (including Siddha) or Unani drugs shall be identified and tested, wherever tests are available for their genuineness, and records of such tests as are carried out for the purpose and the methods thereof shall be maintained.

Raw materials used in the preparation of Ayurvedic (including Siddha) or Unani drugs shall be identified and tested, wherever tests are available for their genuineness, and records of such tests as are carried out for the purpose and the methods thereof shall be maintained. [PART XVIA 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 160-A. Application for grant of approval for testing Ayurvedic, Siddha and Unani drugs. Application for grant or renewal of approval for carrying out tests for identity, purity, quality and strength of Ayurvedic, Siddha and Unani drugs or the raw materials used in the manufacture thereof on behalf of licensees for manufacture for sale of the said Ayurvedic, Siddha and Unani drugs, shall be made in Form 47 to the Licensing Authority appointed by the State Government for the purposes of Part XVI, XVII or XVIII of these rules, as the case may be, and referred to as the 'approving authority' under this Part and shall be accompanied by an inspection fee of six thousand rupees in respect of the drugs specified in the books prescribed in First Schedule to the Act. 1. Ins. by.G.S.R. 331(E) dt. 8.5.1984. 2. Ins. by G.S.R. 701(E), dt. 27-7-2001 and subs. by G.S.R.73 (E), dt. 31-01-2003.
Provided that the applicant shall furnish to the approving authority such additional information as may be required by it in connection with the application in Form 47:
Provided further that if the applicant applies for renewal of approval after its expiry but within six months of such expiry, the inspection fee payable shall be six thousand rupees plus an additional inspection fee at the rate of one thousand rupees per month in the case of testing of Ayurvedic, Siddha and Unani drugs specified in First Schedule to the Act.
Explanation. - For the purpose of this Part, the words "Ayurvedic, Siddha and Unani drugs" shall also mean and include the raw materials used in the manufacture of Ayurvedic, Siddha and Unani drugs, as the case may be.
Section 160, The Drugs and Cosmetics Act and Rules (Act 23 of 1940).

Questions about Section 160

What does Section 160 of the Drugs and Cosmetics Act and Rules deal with?

Section 160 of the Drugs and Cosmetics Act and Rules is headed "Identification of raw materials". Raw materials used in the preparation of Ayurvedic (including Siddha) or Unani drugs shall be identified and tested, wherever tests are available for their genuineness, and records of such tests as are carried out for the purpose and the methods thereof shall be maintained.

How do I find court cases under Section 160 of the Drugs and Cosmetics Act and Rules?

In judgments and charge sheets this section is written several ways, and each form finds a different set of orders. These search the full text of every order eCourtsIndia holds, best matches first: Drugs Cosmetics Act Rules 160, section 160 Drugs Cosmetics Act Rules, section 160 of the Drugs and Cosmetics Act and Rules. Each opens the full list of orders on eCourtsIndia, where it can be narrowed by court, year and outcome.

When was the Drugs and Cosmetics Act and Rules enacted?

Drugs and Cosmetics Act and Rules was enacted in 1940 as Act 23 of 1940. India Code records no commencement date for it. It is in force as at the date shown on this page.

Other sections of this Act

168. 134147 words
54. Form of order not to dispose of stock11273 words
74A. Conditions for licence in Form 25-B5837 words
18. Prohibition of manufacture and sale of certain drugs and cosmetics5197 words
68B. Delegation of Powers by the Central Licence Approving Authority4452 words
65. Condition of licences3128 words

Source and method. Compiled from the enactments of Parliament and of the State legislatures as published on India Code, and republished together with commentary and other original matter under section 52(1)(q)(ii) of the Copyright Act, 1957. Structured, cross-referenced and maintained by eCourtsIndia. Read from the Government's own scanned gazette with Azure Document Intelligence, then split into sections by their numbering. India Code publishes no text for this Act. The scan itself is mirrored into our own storage and served at /scan/053728db-416d-4003-acca-99b3d6b7df6f.pdf, so the reading here can be checked against the page it came from without depending on India Code's own copy staying where it is (it was at https://indiacode.gov.in/server/api/core/bitstreams/2cd6c2e9-226a-4ecd-badb-d1db92507328/content). This page is not a substitute for legal advice.