This document summarizes the Drugs and Magic Remedies (Objectionable Advertisements) Act of 1954 in India. The act prohibits advertising of drugs or remedies that claim medical or magical properties, including for miscarriage, contraception, sexual pleasure, or curing diseases. It establishes penalties for violations, including fines and imprisonment. The act gives authorities power to seize documents with prohibited advertisements and exempt certain products if public interest requires. In 2009, a court in Kerala convicted the MD of a company for violating this act by advertising an herbal aphrodisiac.
Codes of pharmaceutical ethics
In relation to his trade
In relation to his Job
In relation to his Profession
In relation to Medical Profession
Pharmacist's Oath
Codes of pharmaceutical ethics
In relation to his trade
In relation to his Job
In relation to his Profession
In relation to Medical Profession
Pharmacist's Oath
Medicinal and toilet preparations act and rules,1955Ganesh Shevalkar
It is an Act with provision for levy and collection of excise duties on medicinal and toilet preparations containing alcohol, opium, Indian hemp (cannabis) or other narcotic drugs.
Prohibited Advertisements under the Drug & Magic remedies Act 1954:-
Prohibition of Advertisement of Certain Drugs for Treatment of Certain Diseases and Disorders:-
The procurement of miscarriage in women or prevention of conception in women; or
The maintenance or improvement of the capacity of human beings for sexual pleasure;
The correction of menstrual disorder in women; or
The diagnosis, cure, mitigation, treatment or prevention of any disease, disorder or condition specified in the Schedule, or any other disease, disorder or condition which may be specified in the rules made under this Act (Sch. J).
At the end of the 19th century and early 20 century use of Allopathy system increases
Drugs of natural origin: Veg, mineral oil and animals
At that time, profit became main motive than service
Overdose of quinine.A Central law to control drugs and pharmacy profession.
A presentation aimed at providing information with regards to the Pharmacy Act, 1948.
-INTRODUCTION
-HISTORY OF THE ACT
-PHARMACY COUNCIL OF INDIA
-STATE PHARMACY COUNCIL
-SPECIAL PROVISIONS OF THE ACT
-OFFENCES AND PENALTIES
-CONCLUSION
-REFERENCES
NARCOTIC DRUGS AND PSYCHOTROPIC SUBSTANCES ACT (NDPS), 1985 WITH RULE Sagar Savale
The Central Acts like Opium Act, 1857,the Opium Act ,1878 and the Dangerous Drugs Act,1930 were enacted a long time ago. With the changing circumstances and the developments in the field illicit drug traffic and drug abuse at national and international level ,many drawbacks have come to notice in the said Acts.
The Government of India has repealed these old Acts and passed “The Narcotic Drugs and Psychotropic Substances Act,1985’’.
These Acts established in 14 November 1985.
Drugs and Cosmatic Act,1940 and its rules 1945TameshSonkar
Objectives, Definitions, Legal definitions of schedules to the Act and Rules
Import of drugs Classes of drugs and cosmetics prohibited from import
,Import under license or permit. Offences and penalties.
Manufacture of drugs Prohibition of manufacture and sale of certain drugs
Conditions for grant of license and conditions of license for manufacture of
drugs, Manufacture of drugs for test, examination and analysis
,manufacture of new drug, loan license and repacking license.
The Prevention of Cruelty to Animals Act, 1960, authored by acclaimed dancer and animal lover, Rukmini Devi Arundale, is an Act of the Parliament of India enacted in 1960 to prevent the infliction of unnecessary pain or suffering on animals and to amend the laws relating to the prevention of cruelty to animals.
The prevention of cruelty to animals act 1960Shaik Rasheed
This presentation give the complete information regarding the The Prevention of Cruelty to Animals Act 1960 including the definitions, composition of IAEC, Breeding and stocking of animals, experiments, offences and penalties.
This is the pdf of NARCOTIC DRUGS AND PSYCHOTROPIC SUBSTANCES ACT-1985 AND RULES.
OBJECTIVE:-
The Narcotic Drugs and Psychotropic Substances Act, 1985, commonly referred to as the NDPS Act, is an Act of the Parliament of India that prohibits a person from the production, manufacturing, cultivation, possession, sale, purchasing, transport, storage, and consumption of any narcotic drug or psychotropic substance.
AUTHORITIES AND OFFICERS:-
Officers of Central Government—
Without prejudice to the provisions of sub-section (3) of section 4, the Central Government shall appoint a Narcotics Commissioner and may also appoint such other officers with such designations as it thinks fit for this Act.
The Narcotics Commissioner shall, either by himself or through officers subordinate to him, exercise all powers and perform all functions relating to the superintendence of the cultivation of the opium poppy and production of opium and shall also exercise and perform such other powers and functions as may be entrusted to him by the Central Government.
The officers appointed under sub-section (1) shall be subject to the general control and direction of the Central Government, or, if so directed by that Government, also of the Board or any other authority or officer.
Officers of State Government:-
(1) The State Government may appoint such officers with such designations as it thinks fit for this Act.
(2) The officers appointed under sub-section (1) shall be subject to the general control and direction of the State Government, or, if so directed by that Government, also of any other authority or officer.
CONSTITUTION & FUNCTIONS OF NARCOTIC AND PSYCHOTROPIC CONSULTATIVE COMMITTEE:-
The Central Government may constitute, by notification in the Official Gazette, an advisory committee to be called “The Narcotic Drugs and Psychotropic Substances Consultative Committee ” to advise the Central Government on such matters relating to the administration of this Act as are referred to it by that Government from time to time.
The Committee shall consist of a Chairman and such other members, not exceeding twenty, as may be appointed by the Central Government.
The Committee shall meet when required to do so by the Central Government and shall have the power to regulate its procedure.
The Committee may if it deems it necessary so to do for the efficient discharge of any of its functions, constitute one or more sub-committees and may appoint to any such sub-committee, whether generally or for the consideration of any particular matter, any person (including a non-official) who is not a member of the Committee.
NATIONAL FUND FOR CONTROL OF DRUG ABUSE—
The Central Government may, by notification in the Official Gazette, constitute a Fund to be called the National Fund for Control of Drug Abuse.
the sale proceeds of any property forfeited under Chapter VA, any grants that may be made by any person or institution.
Drugs and Magic Remedies (Objectionable Advertisements), 1954 Act,1954 Sagar Savale
An Act to control the advertisement of drugs in certain cases, to prohibit the advertisement for certain purposes of remedies alleged to possess magic qualities and to provide for matters connected therewith. This act is not unconstitutional, because it does not interferes with private business and also it does not impose unreasonable restrictions.
Medicinal and toilet preparations act and rules,1955Ganesh Shevalkar
It is an Act with provision for levy and collection of excise duties on medicinal and toilet preparations containing alcohol, opium, Indian hemp (cannabis) or other narcotic drugs.
Prohibited Advertisements under the Drug & Magic remedies Act 1954:-
Prohibition of Advertisement of Certain Drugs for Treatment of Certain Diseases and Disorders:-
The procurement of miscarriage in women or prevention of conception in women; or
The maintenance or improvement of the capacity of human beings for sexual pleasure;
The correction of menstrual disorder in women; or
The diagnosis, cure, mitigation, treatment or prevention of any disease, disorder or condition specified in the Schedule, or any other disease, disorder or condition which may be specified in the rules made under this Act (Sch. J).
At the end of the 19th century and early 20 century use of Allopathy system increases
Drugs of natural origin: Veg, mineral oil and animals
At that time, profit became main motive than service
Overdose of quinine.A Central law to control drugs and pharmacy profession.
A presentation aimed at providing information with regards to the Pharmacy Act, 1948.
-INTRODUCTION
-HISTORY OF THE ACT
-PHARMACY COUNCIL OF INDIA
-STATE PHARMACY COUNCIL
-SPECIAL PROVISIONS OF THE ACT
-OFFENCES AND PENALTIES
-CONCLUSION
-REFERENCES
NARCOTIC DRUGS AND PSYCHOTROPIC SUBSTANCES ACT (NDPS), 1985 WITH RULE Sagar Savale
The Central Acts like Opium Act, 1857,the Opium Act ,1878 and the Dangerous Drugs Act,1930 were enacted a long time ago. With the changing circumstances and the developments in the field illicit drug traffic and drug abuse at national and international level ,many drawbacks have come to notice in the said Acts.
The Government of India has repealed these old Acts and passed “The Narcotic Drugs and Psychotropic Substances Act,1985’’.
These Acts established in 14 November 1985.
Drugs and Cosmatic Act,1940 and its rules 1945TameshSonkar
Objectives, Definitions, Legal definitions of schedules to the Act and Rules
Import of drugs Classes of drugs and cosmetics prohibited from import
,Import under license or permit. Offences and penalties.
Manufacture of drugs Prohibition of manufacture and sale of certain drugs
Conditions for grant of license and conditions of license for manufacture of
drugs, Manufacture of drugs for test, examination and analysis
,manufacture of new drug, loan license and repacking license.
The Prevention of Cruelty to Animals Act, 1960, authored by acclaimed dancer and animal lover, Rukmini Devi Arundale, is an Act of the Parliament of India enacted in 1960 to prevent the infliction of unnecessary pain or suffering on animals and to amend the laws relating to the prevention of cruelty to animals.
The prevention of cruelty to animals act 1960Shaik Rasheed
This presentation give the complete information regarding the The Prevention of Cruelty to Animals Act 1960 including the definitions, composition of IAEC, Breeding and stocking of animals, experiments, offences and penalties.
This is the pdf of NARCOTIC DRUGS AND PSYCHOTROPIC SUBSTANCES ACT-1985 AND RULES.
OBJECTIVE:-
The Narcotic Drugs and Psychotropic Substances Act, 1985, commonly referred to as the NDPS Act, is an Act of the Parliament of India that prohibits a person from the production, manufacturing, cultivation, possession, sale, purchasing, transport, storage, and consumption of any narcotic drug or psychotropic substance.
AUTHORITIES AND OFFICERS:-
Officers of Central Government—
Without prejudice to the provisions of sub-section (3) of section 4, the Central Government shall appoint a Narcotics Commissioner and may also appoint such other officers with such designations as it thinks fit for this Act.
The Narcotics Commissioner shall, either by himself or through officers subordinate to him, exercise all powers and perform all functions relating to the superintendence of the cultivation of the opium poppy and production of opium and shall also exercise and perform such other powers and functions as may be entrusted to him by the Central Government.
The officers appointed under sub-section (1) shall be subject to the general control and direction of the Central Government, or, if so directed by that Government, also of the Board or any other authority or officer.
Officers of State Government:-
(1) The State Government may appoint such officers with such designations as it thinks fit for this Act.
(2) The officers appointed under sub-section (1) shall be subject to the general control and direction of the State Government, or, if so directed by that Government, also of any other authority or officer.
CONSTITUTION & FUNCTIONS OF NARCOTIC AND PSYCHOTROPIC CONSULTATIVE COMMITTEE:-
The Central Government may constitute, by notification in the Official Gazette, an advisory committee to be called “The Narcotic Drugs and Psychotropic Substances Consultative Committee ” to advise the Central Government on such matters relating to the administration of this Act as are referred to it by that Government from time to time.
The Committee shall consist of a Chairman and such other members, not exceeding twenty, as may be appointed by the Central Government.
The Committee shall meet when required to do so by the Central Government and shall have the power to regulate its procedure.
The Committee may if it deems it necessary so to do for the efficient discharge of any of its functions, constitute one or more sub-committees and may appoint to any such sub-committee, whether generally or for the consideration of any particular matter, any person (including a non-official) who is not a member of the Committee.
NATIONAL FUND FOR CONTROL OF DRUG ABUSE—
The Central Government may, by notification in the Official Gazette, constitute a Fund to be called the National Fund for Control of Drug Abuse.
the sale proceeds of any property forfeited under Chapter VA, any grants that may be made by any person or institution.
Drugs and Magic Remedies (Objectionable Advertisements), 1954 Act,1954 Sagar Savale
An Act to control the advertisement of drugs in certain cases, to prohibit the advertisement for certain purposes of remedies alleged to possess magic qualities and to provide for matters connected therewith. This act is not unconstitutional, because it does not interferes with private business and also it does not impose unreasonable restrictions.
The Drugs and Magic Remedies (Objectionable Advertisements) Act is an Act No. 21 of 1954, which came in force on 1st of April 1955.
AIM: To control the Ad. Of drugs in certain cases, to prohibit the ads. For certain purposes for remedies alleged to possess magic qualities & to provide for related matters
Drug and magic remedies (objectionable advertisement) act 1954 and rules 1955Dr. Ambekar Abdul Wahid
Definitions, Class of Prohibitions Advertisement - Section 3, Classes of exempted advertisements, Powers of entry, search etc., Offenses and penalties, Scrutiny of misleading advertisements relating to drugs, Manner in which advertisements may be sent confidentially, Case Studies.
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The Importance of Community Nursing Care.pdfAD Healthcare
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The dimensions of healthcare quality refer to various attributes or aspects that define the standard of healthcare services. These dimensions are used to evaluate, measure, and improve the quality of care provided to patients. A comprehensive understanding of these dimensions ensures that healthcare systems can address various aspects of patient care effectively and holistically. Dimensions of Healthcare Quality and Performance of care include the following; Appropriateness, Availability, Competence, Continuity, Effectiveness, Efficiency, Efficacy, Prevention, Respect and Care, Safety as well as Timeliness.
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Explore our infographic on 'Essential Metrics for Palliative Care Management' which highlights key performance indicators crucial for enhancing the quality and efficiency of palliative care services.
This visual guide breaks down important metrics across four categories: Patient-Centered Metrics, Care Efficiency Metrics, Quality of Life Metrics, and Staff Metrics. Each section is designed to help healthcare professionals monitor and improve care delivery for patients facing serious illnesses. Understand how to implement these metrics in your palliative care practices for better outcomes and higher satisfaction levels.
Medical Technology Tackles New Health Care Demand - Research Report - March 2...pchutichetpong
M Capital Group (“MCG”) predicts that with, against, despite, and even without the global pandemic, the medical technology (MedTech) industry shows signs of continuous healthy growth, driven by smaller, faster, and cheaper devices, growing demand for home-based applications, technological innovation, strategic acquisitions, investments, and SPAC listings. MCG predicts that this should reflects itself in annual growth of over 6%, well beyond 2028.
According to Chris Mouchabhani, Managing Partner at M Capital Group, “Despite all economic scenarios that one may consider, beyond overall economic shocks, medical technology should remain one of the most promising and robust sectors over the short to medium term and well beyond 2028.”
There is a movement towards home-based care for the elderly, next generation scanning and MRI devices, wearable technology, artificial intelligence incorporation, and online connectivity. Experts also see a focus on predictive, preventive, personalized, participatory, and precision medicine, with rising levels of integration of home care and technological innovation.
The average cost of treatment has been rising across the board, creating additional financial burdens to governments, healthcare providers and insurance companies. According to MCG, cost-per-inpatient-stay in the United States alone rose on average annually by over 13% between 2014 to 2021, leading MedTech to focus research efforts on optimized medical equipment at lower price points, whilst emphasizing portability and ease of use. Namely, 46% of the 1,008 medical technology companies in the 2021 MedTech Innovator (“MTI”) database are focusing on prevention, wellness, detection, or diagnosis, signaling a clear push for preventive care to also tackle costs.
In addition, there has also been a lasting impact on consumer and medical demand for home care, supported by the pandemic. Lockdowns, closure of care facilities, and healthcare systems subjected to capacity pressure, accelerated demand away from traditional inpatient care. Now, outpatient care solutions are driving industry production, with nearly 70% of recent diagnostics start-up companies producing products in areas such as ambulatory clinics, at-home care, and self-administered diagnostics.
Defecation
Normal defecation begins with movement in the left colon, moving stool toward the anus. When stool reaches the rectum, the distention causes relaxation of the internal sphincter and an awareness of the need to defecate. At the time of defecation, the external sphincter relaxes, and abdominal muscles contract, increasing intrarectal pressure and forcing the stool out
The Valsalva maneuver exerts pressure to expel faeces through a voluntary contraction of the abdominal muscles while maintaining forced expiration against a closed airway. Patients with cardiovascular disease, glaucoma, increased intracranial pressure, or a new surgical wound are at greater risk for cardiac dysrhythmias and elevated blood pressure with the Valsalva maneuver and need to avoid straining to pass the stool.
Normal defecation is painless, resulting in passage of soft, formed stool
CONSTIPATION
Constipation is a symptom, not a disease. Improper diet, reduced fluid intake, lack of exercise, and certain medications can cause constipation. For example, patients receiving opiates for pain after surgery often require a stool softener or laxative to prevent constipation. The signs of constipation include infrequent bowel movements (less than every 3 days), difficulty passing stools, excessive straining, inability to defecate at will, and hard feaces
IMPACTION
Fecal impaction results from unrelieved constipation. It is a collection of hardened feces wedged in the rectum that a person cannot expel. In cases of severe impaction the mass extends up into the sigmoid colon.
DIARRHEA
Diarrhea is an increase in the number of stools and the passage of liquid, unformed feces. It is associated with disorders affecting digestion, absorption, and secretion in the GI tract. Intestinal contents pass through the small and large intestine too quickly to allow for the usual absorption of fluid and nutrients. Irritation within the colon results in increased mucus secretion. As a result, feces become watery, and the patient is unable to control the urge to defecate. Normally an anal bag is safe and effective in long-term treatment of patients with fecal incontinence at home, in hospice, or in the hospital. Fecal incontinence is expensive and a potentially dangerous condition in terms of contamination and risk of skin ulceration
HEMORRHOIDS
Hemorrhoids are dilated, engorged veins in the lining of the rectum. They are either external or internal.
FLATULENCE
As gas accumulates in the lumen of the intestines, the bowel wall stretches and distends (flatulence). It is a common cause of abdominal fullness, pain, and cramping. Normally intestinal gas escapes through the mouth (belching) or the anus (passing of flatus)
FECAL INCONTINENCE
Fecal incontinence is the inability to control passage of feces and gas from the anus. Incontinence harms a patient’s body image
PREPARATION AND GIVING OF LAXATIVESACCORDING TO POTTER AND PERRY,
An enema is the instillation of a solution into the rectum and sig
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1. DRUG AND MAGIC REMEDIES
ACT [1954]
-PRESENTED BY,
THARANI.R,
MHA-I Yr,
Dr.N.G.P.ASC.
2. DRUGS & MAGIC REMEDIES ACT (OBJECTIONABLE ADVERTISEMENT) ACT
(1954):
Citation : Act NO. 21 of 1954
Territorial Extend : India (expect) Jammu & Kashmir
Date of Commenced : 1 April 1955
Bill published on : 30 April 1954
This act controls the advertisement of drugs and remedies that claim to have medical
properties and makes doing so as a cognizable offence.
3. This act prohibits the advertisement of products that claim have medical or magical properties.(eg.:
talisman, mantra, amulet)
TALISMAN MANTRA AMULET
4. The law prohibits advertising of drugs and remedies for,
Including miscarriage and prevention of conception in women.
Improving or maintaining the capacity of sexual pleasure.
Correction of menstural disorders.
Curing, diagnosing and preventing any disease
( a list of 54 diseases is included in the law)
5. SECTION 1: SHORT TITLE, EXTENT AND COMMENCEMENT
This Act may be called the Drugs and Magic Remedies (Objectionable
Advertisements) Act, 1954.
It extends to the whole of India except the State of Jammu and Kashmir, and
applies also to persons domiciled in the territories to which this Act extends who
are outside the said territories.
It shall come into force on such date as the Central Government may, be
notification in the Official Gazette, appoint.
6. SECTION 2: DEFINITIONS
'advertisement' includes any notice, circular, label, wrapper, or other document, and any
announcement made orally or by any means of producing or transmitting light, sound or
smoke.
'drug' includes-a medicine for the internal or external use of human beings or animals.
'magic remedy' includes a talisman, mantra, amulet, and any other charm of any kind
which is alleged to possess miraculous powers .
'taking any part in the publication of any advertisement’ – printing of advertisement.
'venereal disease' includes syphilis, gonorrhoea, soft chancre, venereal granuloma and
lympho granuloma.
7. SECTION 3: PROHIBITION OF ADVERTISEMENT OF CERTAIN
DRUGS FOR TREATMENT OF CERTAIN DISEASES AND
DISORDERS
the procurement of miscarriage in women or prevention of conception in
women;
the maintenance or improvement of the capacity of human beings for sexual
pleasure;
the correction of menstrual disorder in women;
the diagnosis, cure, mitigation, treatment or prevention of any venereal disease
or any other disease or condition which may be specified in rules made under
this Act.
8. SECTION 4:PROHIBITION OF MISLEADING ADVERTISEMENTS
RELATING TO DRUGS
directly or indirectly gives a false impression regarding the true character of the
drug;
makes a false claim for the drug;
is otherwise false or misleading in any material particular.
9. SECTION 5:PROHIBITION OFADVERTISEMENT OF MAGIC
REMEDIES FOR TREATMENT OF CERTAIN DISEASES AND
DISORDERS
No person carrying on or purporting to carry on the profession of administering
magic remedies shall take any part in the publication of any advertisement
referring to any magic remedy which directly which directly or indirectly claims
to be efficacious for any of the purposes specified in section 3.
10. SECTION 6:PROHIBITION OF IMPORT INTO, AND EXPORT FROM,
INDIA OF CERTAIN
advertisements - No person shall import into, or export from, the territories to
which this Act extends any document containing an advertisement of the nature
referred to in section 3, or section 4, or section 5, and any documents containing
any such advertisements shall be deemed to be the goods of which the import or
export has been prohibited under section 19 of the Sea Customs Act, 1878 (VIII of
1878) and all the provisions of the Act shall have effect accordingly, except that
section 183 thereof shall have effect as if for the word 'shall' therein the word 'may'
were substituted.
11. SECTION 7:PENALTY
Whoever contravenes any of the provisions of this Act shall, on conviction, be
punishable
In the case of a first conviction, with imprisonment which may extend to six
months, or with fine, or with both;
In the case of subsequent conviction, with imprisonment which may extend to
one year or with fine, or with both.
12. SECTION 8:CONFISCATION OF DOCUMENTS, ETC., CONTAINING
ADVERTISEMENTS PROHIBITED BY THIS ACT
Any person authorised by the State Government in this behalf may, at any time,
seize and detain any document, article or thing which such person has reason to
believe contains any advertisement which contravenes any of the provisions of
this Act and the court trying such contravention may direct that such document
(including all copies thereof), article or thing shall be forfeited to the
Government.
13. SECTION 9:OFFENCES BY COMPANIES
If the person contravening any of the provisions of this Act is a company, the company
shall be deemed to be guilty of the contravention and shall be liable to be proceeded
against and punished accordingly.
Notwithstanding anything contained in sub-section (1) where an offence under this Act
has been committed by a company and it is proved that the offence was committed with
the officer of the company shall also be deemed to be guilty of that offence and shall be
liable to be proceeded against and punished accordingly.
14. SECTION 10:JURDISCTION TO TRY OFFENCES
No court inferior to that of a presidency magistrate or a magistrate of the first
class shall try any offence punishable under this Act.
SECTION 11:OFFICERS TO BE DEEMED TO THE PUBLIC
SERVANTS
Every person authorised under Section 8 shall be deemed to be a public servant
within the meaning of section 21 of the Indian Penal Code (Act XLV of 1860).
15. SECTION 12:INDEMNITY
No suit, prosecution or other legal proceeding shall lie against any person for
anything which is in good faith done or intended to be done under this Act.
SECTION 13:OTHER LAWS NOT AFFECTED
The provisions of this Act are in addition to , and not in derogation of the
provisions of any other law for the time being in force.
16. SECTION 14:SAVINGS
(1) Nothing in this Act shall apply to
(a) any sign board or notice displayed by a registered medical practitioner or his
premises indicating that treatment for any of the diseases or disorders specified in
section 3 is undertaken in those premises; or
(b) any treatise or book dealing with any of the matters specified in section 3 from
a bona fide scientific or social standpoint.
17. SECTION 15:POWER TO EXEMPT FROM APPLICATION OF ACT
If in the opinion of the Central Government public interest requires that the
advertisement of any specified drug or class of drugs should be permitted, it may ,
by notification in the Official Gazette, direct that the provisions of sections 3,4,5
and 6 or any one of such provisions shall not apply or shall apply subject to such
conditions as may be specified in the notification to or in relation to the
advertisement of any such drugs or class of drugs.
18. SECTION 16:POWER TO MAKE RULES
(1) The Central Government may, by notification in the Official Gazette, make rule
for carrying out the purposes of this Act.
(2) In particular and without prejudice to the generality of the foregoing power,
such rules may-
(a) specify any disease or condition to which the provisions of section 3 shall
apply;
(b) prescribe the manner in which advertisements of articles or things referred to in
clause (c) of sub-section (1) of section 14 may be sent confidentially.
19. MD of Kunnath Pharmaceuticals convicted for violation of Magic Remedies
Act
The case against the company was charged by the Ernakulam zonal office of the
Department of Ayurveda Drugs Control, Government of Kerala in 2009.
The Additional Chief Judicial Magistrate Court (EO) at Eranakulam in Kerala
convicted the Proprietor and Licencee of ‘Musli Power Xtra’, a herbal
aphrodisiac, manufactured by Kunnath Pharmaceuticals in Kerala for violation of
provisions of Drugs and Magic Remedies (Objectionable Advertisement) Act,
1954.
The Court has imposed a penalty of Rs.50,000 and also imposed jail sentence of
four months on the Proprietor, KC Abraham. In default of payment of the
amount, Abraham will have to undergo rigorous imprisonment of a period of
three months more, the judgement says.