This document summarizes the key aspects of the Medicinal and Toilet Preparation (excise duty) Act 1955 and Rules thereunder 1976 in India. It outlines the objectives of controlling alcohol use and ensuring uniform excise duties. Manufacturing can occur via bonded or non-bonded licenses, with strict rules for plant setup, record keeping, and excise officer oversight. Export of alcoholic medicines is allowed with duty rebates. Various offenses and penalties are also defined for non-compliance by licensees or officers.
Medicinal and toilatory preparation act 1955 Suvarta Maru
This document discusses the Medicinal and Toilet Preparation Act of 1955 and related rules from 1976 regarding the production and regulation of alcoholic preparations in India. It outlines key definitions including bonded and non-bonded manufactories. There are two modes of manufacturing preparations containing alcohol - in bond, using untaxed alcohol under excise supervision, or outside bond using taxed alcohol. The licensing process and ideal facility requirements are described. Responsibilities of excise officers who oversee the facilities and powers granted to them are also summarized.
There are two modes of manufacturing medical and toilet preparations containing alcohol: manufacturing in bond or non-bonded. Manufacturing in bond requires facilities like a spirit store, manufacturing rooms, storage rooms, and compliance with security measures. Alcohol is obtained from approved distilleries and stored in the bonded laboratory where it is measured and issued for production. Final products are stored and sampled before being issued, with duties paid based on alcohol content. Wastage is regulated and recovered alcohol can be reused or destroyed if unfit.
4 medicinal and toilet preparation act 1955Charudatta Jog
This document outlines the Medicinal & Toilet Preparation Act of 1955, which was passed to standardize excise duties across states in India. The key objectives of the act were to levy and collect duties on alcohol used in medicinal and toilet preparations and curb irregularities. The act established procedures for licensing the manufacture of preparations containing alcohol or narcotics. It also differentiated between manufacturing processes that took place within bonded laboratories versus outside of them, and outlined exemptions, duties, and responsibilities of excise officers in enforcing the act.
medicinal and toilet preparation act 1955.pptHarshadaa bafna
The Medicinal and Toilet Preparation Act of 1955 and Rules of 1976 provide for the levy and collection of excise duties on medicinal and toilet preparations containing alcohol, opium, or other narcotic drugs. It defines key terms and outlines rules for the licensed manufacture of such preparations in bonded or non-bonded facilities. The Act specifies procedures for obtaining alcohol, manufacturing, storing, transporting, and exporting goods. It also describes the powers, duties, and responsibilities of excise officers in implementing and enforcing the Act.
This document summarizes the key points of the Medicinal & Toilet preparations act of 1955 and rules thereunder from 1976 regarding the production of medicines and toiletries containing alcohol or other substances. It defines key terms, outlines the licensing process for bonded and non-bonded laboratories, and describes the requirements for facilities. Offenses and penalties are also specified for licensees, excise officers, and the public. The overall objective is to regulate the use of substances like alcohol in medical and personal care products through a licensing and inspection process, as well as by defining illegal activities and associated penalties.
The Medicinal and Toilet Preparation Act of 1955 was enacted to regulate and control the use of alcohol in medicinal and toilet preparations in India. The objectives of the Act were to provide uniform rules and rates of excise duties on preparations containing alcohol, drugs, or narcotics. It aimed to curb misuse of alcohol and ensure its transport, issue, and use were properly controlled. The Act defined key terms like "alcohol" and types of medicinal and toilet preparations. It also provided powers to excise officers to inspect premises, enter/search/seize items, suspend/revoke licenses, and prosecute violations. Manufacturers had to obtain licenses to produce items in bonded or non-bonded facilities depending on
The document summarizes the key aspects of the Prevention of Cruelty to Animals Act of 1960 in India. It outlines the objectives of preventing unnecessary pain or suffering to animals. It defines important terms like animals and cruelty. It describes the composition and functions of the Institutional Animal Ethics Committee, which approves animal experimentation protocols. It provides guidelines on breeding, stocking, and experimentation with animals. It discusses the requirements for transferring or acquiring animals, maintaining records, and the powers and penalties around suspending or revoking registrations of establishments that violate the act.
This document provides an overview of the administration of the Drugs and Cosmetics Act and Rules in India. It discusses the roles of various analytical, executive, and advisory bodies involved in drug regulation. It also outlines the qualifications, duties, and powers of key regulatory positions like Government Analysts, Drugs Inspectors, and the procedures they follow to inspect facilities, collect samples, test drugs, and take action if drugs are found to be substandard.
Medicinal and toilatory preparation act 1955 Suvarta Maru
This document discusses the Medicinal and Toilet Preparation Act of 1955 and related rules from 1976 regarding the production and regulation of alcoholic preparations in India. It outlines key definitions including bonded and non-bonded manufactories. There are two modes of manufacturing preparations containing alcohol - in bond, using untaxed alcohol under excise supervision, or outside bond using taxed alcohol. The licensing process and ideal facility requirements are described. Responsibilities of excise officers who oversee the facilities and powers granted to them are also summarized.
There are two modes of manufacturing medical and toilet preparations containing alcohol: manufacturing in bond or non-bonded. Manufacturing in bond requires facilities like a spirit store, manufacturing rooms, storage rooms, and compliance with security measures. Alcohol is obtained from approved distilleries and stored in the bonded laboratory where it is measured and issued for production. Final products are stored and sampled before being issued, with duties paid based on alcohol content. Wastage is regulated and recovered alcohol can be reused or destroyed if unfit.
4 medicinal and toilet preparation act 1955Charudatta Jog
This document outlines the Medicinal & Toilet Preparation Act of 1955, which was passed to standardize excise duties across states in India. The key objectives of the act were to levy and collect duties on alcohol used in medicinal and toilet preparations and curb irregularities. The act established procedures for licensing the manufacture of preparations containing alcohol or narcotics. It also differentiated between manufacturing processes that took place within bonded laboratories versus outside of them, and outlined exemptions, duties, and responsibilities of excise officers in enforcing the act.
medicinal and toilet preparation act 1955.pptHarshadaa bafna
The Medicinal and Toilet Preparation Act of 1955 and Rules of 1976 provide for the levy and collection of excise duties on medicinal and toilet preparations containing alcohol, opium, or other narcotic drugs. It defines key terms and outlines rules for the licensed manufacture of such preparations in bonded or non-bonded facilities. The Act specifies procedures for obtaining alcohol, manufacturing, storing, transporting, and exporting goods. It also describes the powers, duties, and responsibilities of excise officers in implementing and enforcing the Act.
This document summarizes the key points of the Medicinal & Toilet preparations act of 1955 and rules thereunder from 1976 regarding the production of medicines and toiletries containing alcohol or other substances. It defines key terms, outlines the licensing process for bonded and non-bonded laboratories, and describes the requirements for facilities. Offenses and penalties are also specified for licensees, excise officers, and the public. The overall objective is to regulate the use of substances like alcohol in medical and personal care products through a licensing and inspection process, as well as by defining illegal activities and associated penalties.
The Medicinal and Toilet Preparation Act of 1955 was enacted to regulate and control the use of alcohol in medicinal and toilet preparations in India. The objectives of the Act were to provide uniform rules and rates of excise duties on preparations containing alcohol, drugs, or narcotics. It aimed to curb misuse of alcohol and ensure its transport, issue, and use were properly controlled. The Act defined key terms like "alcohol" and types of medicinal and toilet preparations. It also provided powers to excise officers to inspect premises, enter/search/seize items, suspend/revoke licenses, and prosecute violations. Manufacturers had to obtain licenses to produce items in bonded or non-bonded facilities depending on
The document summarizes the key aspects of the Prevention of Cruelty to Animals Act of 1960 in India. It outlines the objectives of preventing unnecessary pain or suffering to animals. It defines important terms like animals and cruelty. It describes the composition and functions of the Institutional Animal Ethics Committee, which approves animal experimentation protocols. It provides guidelines on breeding, stocking, and experimentation with animals. It discusses the requirements for transferring or acquiring animals, maintaining records, and the powers and penalties around suspending or revoking registrations of establishments that violate the act.
This document provides an overview of the administration of the Drugs and Cosmetics Act and Rules in India. It discusses the roles of various analytical, executive, and advisory bodies involved in drug regulation. It also outlines the qualifications, duties, and powers of key regulatory positions like Government Analysts, Drugs Inspectors, and the procedures they follow to inspect facilities, collect samples, test drugs, and take action if drugs are found to be substandard.
This document summarizes key aspects of the MR. G.A.SHETE MEDICINAL & TOILET PREPARATION Act, including definitions of terms like bonded and non-bonded laboratories, restricted and unrestricted preparations, and dutiable goods. It also outlines requirements for manufacturing medicinal preparations in bonded and non-bonded facilities, as well as various offenses and associated penalties under the Act. Manufacturing in bonded facilities requires an excise license and occurs under excise supervision, while non-bonded manufacturing requires the duty to already be paid. The document provides an overview of the regulatory framework for production and storage of medicinal and toilet preparations containing controlled substances in India.
Medicinal and toilet preparations act and rules,1955 (excise duties)Niveditha Shankar
The document summarizes the Medicinal and Toilet Preparations Act and Rules of 1955 in India. The key points are:
1) The Act provides for uniform excise duties on medicinal and toilet preparations containing alcohol, opium, cannabis, or other narcotics throughout India.
2) Manufacturing such preparations requires a license from excise authorities and following strict rules regarding facilities, storage, record keeping and excise oversight.
3) Excise duties are collected when preparations containing alcohol or narcotics are removed from licensed manufacturing premises, with some exemptions for charitable facilities. Penalties are prescribed for violations.
The document discusses the Medicinal and Toilet Preparations Act of 1955 and related rules from 1976. The Act provides for the collection of excise duties on medicinal and toilet preparations containing alcohol, cannabis, or narcotic drugs. It aims to provide uniform rules and rates of excise duties across India. The document outlines definitions, licensing procedures, and regulations for the manufacture of such preparations in bonded and non-bonded facilities. Strict rules are in place for procuring and storing alcohol and finished products in bonded laboratories.
This act gives an idea about the constitution and functions of PCI. Brief about Education Regulation in India. Registration procedure for the pharmacist in India.
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.
The document discusses various pharmaceutical legislations in India. It provides a brief history of pharmaceutical companies in India from the early 19th century. It then summarizes key committees that shaped drug regulations, including the Drugs Enquiry Committee headed by Col. R.N. Chopra in 1931. The Chopra Committee made recommendations that led to the Drugs Act of 1940, establishing drug control authorities and the regulation of drug manufacturing. Subsequent acts and amendments expanded regulations to areas like pharmacy education and advertising. The overall objective of pharmaceutical legislation in India is to ensure safe, effective and quality-tested drugs for public health.
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.
Non bonded Laboratory
It means the premises or any part of the premises approved & licensed for the manufacture & storage of medicinal & toilet preparations containing alcohol, opium, Indian hemp & other narcotic drugs or narcotics on which duty has been paid.
The document summarizes the key aspects of the Medicinal and Toilet Preparations Act and Rules, 1955 in India. The objectives of the act are to provide for excise duties on medicinal and toilet preparations containing alcohol, narcotics or drugs and to control their manufacture and misuse. The act defines relevant terms and outlines the licensing process and requirements for the manufacture of such preparations both within bonded premises and outside. It also describes the duties and powers of excise officers, search and seizure procedures, offenses and penalties. The schedule lists the categories of dutiable goods and applicable rates of duty.
The document summarizes the Prevention of Cruelty to Animals Act 1960 in India. It outlines the objectives of preventing unnecessary pain/suffering to animals. It defines key terms and outlines the roles and guidelines of Institutional Animal Ethics Committees and the Committee for the Control and Supervision of Experiments on Animals in regulating experiments and care of animals. Infractions are subject to penalties like fines or imprisonment. The overall aim is to ensure humane treatment of animals used in experiments and activities.
The document summarizes the constitution and functions of key organizations under the Drugs and Cosmetics Act of 1940 and Rules of 1945 in India. The Drugs Technical Advisory Board (DTAB) advises the central and state governments and consists of 18 ex-officio and nominated members. The Drugs Consultative Committee (DCC) advises on securing uniformity and consists of central and state government representatives. The Central Drugs Laboratory (CDL) in Kolkata analyzes drug and cosmetic samples sent by courts and customs and maintains reference standards.
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 document summarizes key aspects of the Drug and Cosmetic Act and Rules in India, including:
- The Acts and Rules regulate the import, manufacture, distribution and sale of drugs and cosmetics in India.
- Important definitions are provided for terms like "drug", "cosmetic", "manufacture" and others.
- Drugs and cosmetics can be deemed "misbranded", "adulterated" or "spurious" if they do not meet certain standards.
- The Rules contain 18 parts and 26 schedules providing detailed requirements and guidelines for drugs and cosmetics.
- Key agencies like the Drugs Technical Advisory Board help administer the Acts and
Medicinal & toilet preparation act as per pciShital Kasale
1) The document discusses the Medicinal & Toilet Preparation (Excise Duties) Act of 1955 and rules regarding the manufacture and storage of medicinal and toilet preparations containing alcohol or other substances.
2) It provides definitions for key terms under the act such as alcohol, dutiable goods, medicinal preparations, and outlines licensing procedures and requirements for bonded and non-bonded manufactories.
3) The rules cover obtaining and storing alcohol and finished products, classification of preparations, warehousing, export, and penalties for violations. The goal is to control the use of alcohol for medicinal purposes and prevent misuse.
The application for Registration and import can be made to the Licensing Authority under the Act i.e. to the Drugs Controller General at CDSCO. Drug and Cosmetic Act 1945: It Contains provisions for classification of drugs under given schedules. Guidelines for the storage,sale,display and prescription of each schedule.
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.
Schedule M outlines Good Manufacturing Practices (GMP) that must be followed by pharmaceutical manufacturing units in India. It contains requirements for factory premises, plants, equipment, and quality assurance to ensure products are consistently manufactured and controlled to quality standards. Schedule M has two parts - Part 1 covers GMP for premises and materials, and Part 2 covers specific plant and material requirements. It provides detailed guidelines for facilities, equipment, sanitation, personnel, documentation, manufacturing, quality control, distribution, and more to help ensure therapeutic goods produced meet the required quality standards.
Bonded laboratories are suitable for large-scale manufacture of goods and require supervision from excise staff. They must have four distinct compartments and pay excise duty when goods are removed. Non-bonded laboratories are suitable for small-scale manufacture without excise staff oversight. They require three compartments and pay excise duty upon purchase of raw spirits. Advance security money is needed for bonded laboratories but not for non-bonded ones, though state governments can relax infrastructure requirements for low alcohol production.
This presentation consists of information related to Schedule M, a topic under #Drug_and_Cosmetics_Act. This presentation could be beneficial for the sake of the seminar in #Pharmaceutical_Jurisprudence for pharmacy students.
1) The Medicinal and Toilet Preparation Act of 1955 provides for the collection of excise duties on medicinal and toilet preparations containing alcohol, drugs, or narcotics.
2) It aims to provide uniform excise duty rules and rates throughout India, control the misuse of alcohol, and prevent irregularities seen under the previous Act.
3) Manufacturing of such preparations can be done either in bonded facilities under excise supervision or outside of bonds after payment of duties. Strict rules govern the construction and operation of manufacturing facilities.
This document summarizes key aspects of the MR. G.A.SHETE MEDICINAL & TOILET PREPARATION Act, including definitions of terms like bonded and non-bonded laboratories, restricted and unrestricted preparations, and dutiable goods. It also outlines requirements for manufacturing medicinal preparations in bonded and non-bonded facilities, as well as various offenses and associated penalties under the Act. Manufacturing in bonded facilities requires an excise license and occurs under excise supervision, while non-bonded manufacturing requires the duty to already be paid. The document provides an overview of the regulatory framework for production and storage of medicinal and toilet preparations containing controlled substances in India.
Medicinal and toilet preparations act and rules,1955 (excise duties)Niveditha Shankar
The document summarizes the Medicinal and Toilet Preparations Act and Rules of 1955 in India. The key points are:
1) The Act provides for uniform excise duties on medicinal and toilet preparations containing alcohol, opium, cannabis, or other narcotics throughout India.
2) Manufacturing such preparations requires a license from excise authorities and following strict rules regarding facilities, storage, record keeping and excise oversight.
3) Excise duties are collected when preparations containing alcohol or narcotics are removed from licensed manufacturing premises, with some exemptions for charitable facilities. Penalties are prescribed for violations.
The document discusses the Medicinal and Toilet Preparations Act of 1955 and related rules from 1976. The Act provides for the collection of excise duties on medicinal and toilet preparations containing alcohol, cannabis, or narcotic drugs. It aims to provide uniform rules and rates of excise duties across India. The document outlines definitions, licensing procedures, and regulations for the manufacture of such preparations in bonded and non-bonded facilities. Strict rules are in place for procuring and storing alcohol and finished products in bonded laboratories.
This act gives an idea about the constitution and functions of PCI. Brief about Education Regulation in India. Registration procedure for the pharmacist in India.
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.
The document discusses various pharmaceutical legislations in India. It provides a brief history of pharmaceutical companies in India from the early 19th century. It then summarizes key committees that shaped drug regulations, including the Drugs Enquiry Committee headed by Col. R.N. Chopra in 1931. The Chopra Committee made recommendations that led to the Drugs Act of 1940, establishing drug control authorities and the regulation of drug manufacturing. Subsequent acts and amendments expanded regulations to areas like pharmacy education and advertising. The overall objective of pharmaceutical legislation in India is to ensure safe, effective and quality-tested drugs for public health.
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.
Non bonded Laboratory
It means the premises or any part of the premises approved & licensed for the manufacture & storage of medicinal & toilet preparations containing alcohol, opium, Indian hemp & other narcotic drugs or narcotics on which duty has been paid.
The document summarizes the key aspects of the Medicinal and Toilet Preparations Act and Rules, 1955 in India. The objectives of the act are to provide for excise duties on medicinal and toilet preparations containing alcohol, narcotics or drugs and to control their manufacture and misuse. The act defines relevant terms and outlines the licensing process and requirements for the manufacture of such preparations both within bonded premises and outside. It also describes the duties and powers of excise officers, search and seizure procedures, offenses and penalties. The schedule lists the categories of dutiable goods and applicable rates of duty.
The document summarizes the Prevention of Cruelty to Animals Act 1960 in India. It outlines the objectives of preventing unnecessary pain/suffering to animals. It defines key terms and outlines the roles and guidelines of Institutional Animal Ethics Committees and the Committee for the Control and Supervision of Experiments on Animals in regulating experiments and care of animals. Infractions are subject to penalties like fines or imprisonment. The overall aim is to ensure humane treatment of animals used in experiments and activities.
The document summarizes the constitution and functions of key organizations under the Drugs and Cosmetics Act of 1940 and Rules of 1945 in India. The Drugs Technical Advisory Board (DTAB) advises the central and state governments and consists of 18 ex-officio and nominated members. The Drugs Consultative Committee (DCC) advises on securing uniformity and consists of central and state government representatives. The Central Drugs Laboratory (CDL) in Kolkata analyzes drug and cosmetic samples sent by courts and customs and maintains reference standards.
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 document summarizes key aspects of the Drug and Cosmetic Act and Rules in India, including:
- The Acts and Rules regulate the import, manufacture, distribution and sale of drugs and cosmetics in India.
- Important definitions are provided for terms like "drug", "cosmetic", "manufacture" and others.
- Drugs and cosmetics can be deemed "misbranded", "adulterated" or "spurious" if they do not meet certain standards.
- The Rules contain 18 parts and 26 schedules providing detailed requirements and guidelines for drugs and cosmetics.
- Key agencies like the Drugs Technical Advisory Board help administer the Acts and
Medicinal & toilet preparation act as per pciShital Kasale
1) The document discusses the Medicinal & Toilet Preparation (Excise Duties) Act of 1955 and rules regarding the manufacture and storage of medicinal and toilet preparations containing alcohol or other substances.
2) It provides definitions for key terms under the act such as alcohol, dutiable goods, medicinal preparations, and outlines licensing procedures and requirements for bonded and non-bonded manufactories.
3) The rules cover obtaining and storing alcohol and finished products, classification of preparations, warehousing, export, and penalties for violations. The goal is to control the use of alcohol for medicinal purposes and prevent misuse.
The application for Registration and import can be made to the Licensing Authority under the Act i.e. to the Drugs Controller General at CDSCO. Drug and Cosmetic Act 1945: It Contains provisions for classification of drugs under given schedules. Guidelines for the storage,sale,display and prescription of each schedule.
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.
Schedule M outlines Good Manufacturing Practices (GMP) that must be followed by pharmaceutical manufacturing units in India. It contains requirements for factory premises, plants, equipment, and quality assurance to ensure products are consistently manufactured and controlled to quality standards. Schedule M has two parts - Part 1 covers GMP for premises and materials, and Part 2 covers specific plant and material requirements. It provides detailed guidelines for facilities, equipment, sanitation, personnel, documentation, manufacturing, quality control, distribution, and more to help ensure therapeutic goods produced meet the required quality standards.
Bonded laboratories are suitable for large-scale manufacture of goods and require supervision from excise staff. They must have four distinct compartments and pay excise duty when goods are removed. Non-bonded laboratories are suitable for small-scale manufacture without excise staff oversight. They require three compartments and pay excise duty upon purchase of raw spirits. Advance security money is needed for bonded laboratories but not for non-bonded ones, though state governments can relax infrastructure requirements for low alcohol production.
This presentation consists of information related to Schedule M, a topic under #Drug_and_Cosmetics_Act. This presentation could be beneficial for the sake of the seminar in #Pharmaceutical_Jurisprudence for pharmacy students.
1) The Medicinal and Toilet Preparation Act of 1955 provides for the collection of excise duties on medicinal and toilet preparations containing alcohol, drugs, or narcotics.
2) It aims to provide uniform excise duty rules and rates throughout India, control the misuse of alcohol, and prevent irregularities seen under the previous Act.
3) Manufacturing of such preparations can be done either in bonded facilities under excise supervision or outside of bonds after payment of duties. Strict rules govern the construction and operation of manufacturing facilities.
Medicinal and Toilet Preparations (Excise Duties).pptxDeeptiBhagchandani
This document provides definitions and guidelines related to the Medicinal and Toilet Preparations (Excise Duties) Act, 1955 and rules thereunder in India. It discusses how alcohol is used to manufacture medicines and toilet preparations and the need to control its distribution to prevent misuse. The key objectives of the act are to levy and collect duties on preparations containing alcohol, opium, cannabis, or other narcotic drugs. Manufacturers must obtain licenses and adhere to requirements for bonded or non-bonded facilities regarding building layout, storage, record keeping and more. Rectified spirit is obtained through approved channels and duties may be waived in some cases of bona fide loss.
Medicinal and toilet preparation act (Excise duty actChaitaliAgrawal6
The document provides an overview of the Medicinal and Toilet Preparation Act (Excise Duties) Act. Key points include:
- The act aims to provide uniform rules and rates of excise duties on medicinal and toilet preparations containing alcohol or narcotics across India.
- It defines key terms like alcohol, dutiable goods, medicinal preparations, bonded and non-bonded manufactories.
- The objectives are to provide for collection of excise duties and appointment of officers to oversee manufacturing.
- Manufacturing can only be done under license and involves procurement, storage, and accounting of alcohol as well as sampling and export of finished goods.
- There are penalties for non-compliance with
The document provides an overview of the Medicinal and Toilet Preparation Act (Excise Duties) Act. Key points include:
- The act aims to provide uniform rules and rates of excise duties on medicinal and toilet preparations containing alcohol or narcotics across India.
- It defines key terms like alcohol, dutiable goods, medicinal preparations, and bonded and non-bonded manufactories.
- Manufacturing of such preparations requires a license and can only be done in licensed premises, with duties paid on products removed from bonded facilities.
- The act establishes standards for bonded laboratories and procedures for procuring and storing alcohol, manufacturing and storing products, and exporting goods.
- It also covers
This document outlines the key provisions of the Medicinal and Toilet Preparation (Excise Duties) Act. Some key points:
1. The act was passed in 1955 to standardize excise duties on medicinal and toilet preparations containing alcohol or narcotic drugs across states, preventing interstate smuggling.
2. It defines terms like alcohol, dutiable goods, medicinal preparations, toilet preparations and sets rules for licensing the manufacture of such preparations.
3. Manufacture is allowed either in bonded premises using untaxed alcohol under excise supervision, or outside bonded premises after paying duties. Strict record keeping and security measures are mandated.
Medicinal and toilet preparations (excise duties) act, 1995 and rules, 1956Ravish Yadav
The all the content in this profile is completed by the teachers, students as well as other health care peoples.
thank you, all the respected peoples, for giving the information to complete this presentation.
this information is free to use by anyone.
This document provides an overview of the Medicinal and Toilet Preparation Act of 1955 in India. It discusses how the Act regulates the manufacture and storage of medicinal and toilet preparations containing alcohol. Key points include that preparations can be manufactured in bonded facilities using alcohol without duty or in non-bonded facilities using alcohol with duty paid. Bonded facilities require licenses and must meet certain ideal requirements. The duties of excise officers are also outlined, such as checking qualifications, visiting premises, and countersigning alcohol indents. Powers and responsibilities under the Act are also summarized.
Medicinal and toilet preparation (excise duties)Keerthana Ramesh
The Medicinal and Toilet Preparation Act was passed in 1955 to regulate the production and sale of medicinal and toilet preparations containing alcohol, narcotic drugs, or narcotics. Prior to this act, different states had varying rules for spirituous medicinal preparations, leading to inter-state smuggling. The act established uniform rules across states regarding excise duties and licensing requirements for the manufacture of such preparations. It aimed to control the availability and affordability of alcohol for medicinal and non-medicinal uses.
This document discusses the Medicinal and Toilet Preparations Act of 1955 which established uniform rules and rates for excise duties on preparations containing alcohol across India. It summarizes key aspects of the act including definitions of terms, licensing procedures for manufactories, regulations around production and storage of alcoholic preparations, export procedures, and classifications of ayurvedic, homeopathic, and proprietary preparations. A standing committee is also established to advise the central government on technical administration of the act.
This document summarizes the Medicinal and Toilet Preparation Act of 1955, which was passed to establish uniform excise duties across Indian states. It outlines the licensing procedures and requirements for manufacturing alcoholic preparations both inside and outside of bonded laboratories. Key points include applying for licenses, payment of fees, obtaining and storing alcohol, manufacturing and storage procedures, warehousing of unfinished goods, transport and export rules, and the powers and responsibilities of excise officers in enforcing the act. The overall aim was to regulate the production and distribution of medicines and toiletries containing alcohol.
The Medicinal and Toilet Preparation Act was passed in 1955 to regulate the manufacture and storage of medicinal and toilet preparations containing alcohol or narcotic drugs. The Act has 11 chapters and 21 sections. It defines key terms like alcohol, dutiable goods, and medicinal preparations. It outlines licensing procedures for bonded and non-bonded manufacturing facilities. The Act grants powers to excise officers to inspect premises, search, seize items, and make rules. Manufacturing can take place in bonded facilities without payment of duty. The Act also specifies offenses and penalties for violations like failure to furnish export proof or maintaining false stock accounts.
Legislation in respect of Homeopathic PharmacyRamJyothis
The document summarizes key legislation related to homeopathic pharmacy in India. It discusses the origin of pharmaceutical legislation beginning in 1927 and the recommendations of committees that helped form acts like the Drugs and Cosmetics Act of 1940. The act established standards for importing, manufacturing, and selling drugs and set up licensing for pharmacists. It also covers laws specific to homeopathic medicines regarding licensing of sellers and manufacturers, conditions of licenses, labeling, and restrictions on packaging and alcohol content. The document traces the evolution of drug policy and regulation in India.
This document discusses the Excise Duties Act of 1955 and related rules from 1976 regarding the manufacture and transport of medicinal and toiletry preparations containing alcohol in India. It outlines the licensing requirements, fees, and procedures for manufacturing alcoholic preparations both within bonded laboratories and outside of bonded facilities. The document also addresses warehousing, inter-state transport, export procedures, offenses and penalties defined by the Act, and references several textbooks on pharmaceutical jurisprudence.
Definition of cosmetics.
Regulation provision relating to manufacture of cosmetics
a. How to obtain license
b. Conditions of license
c. Regulatory provision on sale of cosmetics
d. Loan license
Offences and Penalties
The document discusses regulatory provisions for cosmetics in India. Cosmetics are regulated under the Drugs and Cosmetics Act of 1940 and Rules of 1945. The act defines cosmetics and outlines labeling requirements including the name, address, ingredients, directions for use, and batch number. Imports of cosmetics must meet quality standards and cannot contain prohibited ingredients. Manufacturers must obtain licenses from state authorities by meeting facility and equipment requirements. Products must also meet standards set by the Bureau of Indian Standards.
Regulatory provision related to manufacture of cosmeticManish Rajput
cosmetic, regulatory provision, schedule M, condition of licence, schedule U, prohibition of certain cosmetics, misbranded and spurious cosmetics, loan licence, offences and penalties,
Similar to medicinal and toilet preparation act 1995.pptx (20)
This document discusses various inorganic antioxidants. It defines antioxidants as agents that inhibit oxidation and are commonly used to prevent rancidity in oils and fats or deterioration of other materials. It then describes the key properties and uses of several important inorganic antioxidants, including hypo-phosphorous acid, sulphur dioxide, sodium bisulphite, sodium metabisulphite, sodium thiosulphate, nitrogen, and sodium nitrite. For each antioxidant, it provides the chemical formula, how it is obtained, physical and chemical properties, and common applications. The overall document serves as a reference on important inorganic antioxidants used in pharmaceutical and food products.
This document provides an overview of medical terminology for pharmacists. It defines key terms like medicine, disease, and discusses the importance of understanding medical terminology. It also covers classifications of terminology, common word elements like prefixes and suffixes, dosage forms, pharmacological terms and their meanings, and common Latin terms used in medicine. The document aims to familiarize pharmacists with the terminology they will encounter in diagnosing and treating diseases.
This document discusses drug distribution systems in hospitals. It covers both outpatient and inpatient distribution. For outpatients, drugs are dispensed from a pharmacy near the outpatient area. For inpatients, common distribution systems include individual prescriptions, floor stock systems, unit dose systems, and satellite pharmacies located on hospital floors. The goal is to efficiently provide needed drugs to patients while minimizing errors.
This document provides an overview of non-sterile manufacturing processes. It discusses the manufacture of tablets, capsules, liquid orals, and external preparations. The key requirements for the manufacturing area include controlled temperature, humidity, air filtration, cleaning and sanitization. Tablet manufacturing involves mixing, granulation, drying, compression and coating. Capsule manufacturing uses filling machines. Liquid oral production requires mixing tanks, filtration and bottling equipment. External preparations are made using mixing tanks, mills and filling equipment.
This document summarizes the key aspects of sterile manufacture of parenteral products. It describes the types of parenteral preparations, facility requirements including layout and laminar air flow, additives used in formulations, production planning such as cleaning, filling, and sealing processes. It also discusses the quality control tests including sterility, pyrogen, clarity, and leakage tests to ensure the sterile products are free of microorganisms and safe for patient use.
The document discusses various aspects of hospital pharmacy including its definition, functions, objectives, location and layout, requirements and the role of the Pharmacy and Therapeutics Committee. The functions of a hospital pharmacy include purchasing, storage, dispensing, manufacturing, sterile supply, drug information services and records. The objectives are to provide effective pharmacy services and ensure rational and optimal drug therapy for patients. Hospital pharmacies require qualified staff, adequate floor space and equipment to fulfill their roles properly.
This document provides a summary of key information about hospitals, including their definition, functions, classifications, organization, and the health delivery system in India. It defines a hospital as an organization that takes care of people's health and treats diseases using equipment and trained professionals. Hospitals function to treat patients, prevent diseases, train health professionals, conduct medical research, and support public health. They can be classified based on size, ownership, treatment approach, clinical focus, length of stay, and costs. The document also outlines the organizational structure of hospitals and their departments, as well as India's primary, secondary, and tertiary levels of health care delivery.
The document describes the structure and function of key components of the cell, including the cell membrane, cytoplasm, organelles, and nucleus. The cell membrane forms the outer boundary of the cell and regulates the internal environment using a phospholipid bilayer structure. The cytoplasm contains cytosol and various organelles that carry out important functions. Organelles such as mitochondria generate energy, ribosomes synthesize proteins, and the endoplasmic reticulum and Golgi bodies process and transport molecules. The nucleus houses the cell's genetic material and controls cell processes.
hospital instrument and health accessories (5).pdfPriyayannawar4
This document provides an overview of surgical instruments, hospital equipment, diagnostic tools, and health accessories. It discusses the classification of hospital instruments into diagnostic, therapeutic, and operative categories. Diagnostic instruments include endoscopes, CT scans, and biopsy tools. Therapeutic instruments encompass sterilization equipment, sutures, gloves, drains, splints, lasers, and tourniquets. Operative instruments consist of scalpels, scissors, cutters, forceps, and clamps. The document also outlines various health accessories such as hospital beds, wheelchairs, canes, urological supplies, and oxygen therapy equipment.
The document defines various terms related to drug information services, including drug information service (DIS), drug information center (DIC), drug information network (DIN), and drug information bulletin (DIB). It provides examples of each term and discusses the objectives and importance of DICs, which provide drug information to healthcare professionals and patients. Key sources of drug information for DICs are described, including primary sources like research articles and secondary sources like review articles and pharmacopoeias.
clinical pharmacy and modern dispensing practice. ...docxPriyayannawar4
Clinical pharmacy involves providing care and advice to patients regarding their medication therapy to promote health and prevent disease. The clinical pharmacist plays an important role in various areas like making decisions about drug therapy, counseling patients, and ensuring compliance. Some key responsibilities of a clinical pharmacist include taking medication histories, educating patients, monitoring drug therapy, and participating in research. Proper patient counseling and compliance are important to achieve the desired outcomes of medication therapy.
The document defines and describes the respiratory system. It outlines the organs involved like the nose, pharynx, larynx, trachea, lungs and their functions. The document also explains the process of respiration from breathing to gas exchange in the lungs and tissues, and defines various lung volumes like tidal volume, inspiratory reserve volume, vital capacity and more.
The Drug and Magic Remedies Act of 1954 was passed to regulate advertisements of drugs and magic remedies in India by prohibiting advertisements that promote self-medication or treatment of certain diseases, as well as those that mislead people about drugs. The Act defines key terms like advertisement and drug, outlines classes of prohibited and exempted advertisements, and establishes penalties for violations, with increased punishment for repeat offenses. The objective is to control advertisements related to drugs and prohibit misleading advertisements of magic remedies that falsely claim to cure diseases.
This document summarizes the Drug (Price Control) Order of 1995 in India. It establishes schedules that list bulk drugs and formulations subject to price controls. The order's objectives are to ensure adequate production and equitable distribution of drugs, maintain drug supplies, and make drugs available at fair prices. It defines key terms and establishes the formula used to calculate the retail price of scheduled formulations based on material and manufacturing costs. The government has the power to exempt manufacturers from price controls after considering factors like number of employees, capital invested, products made, sales, and production of new drugs. Penalties are established for non-compliance.
The document discusses the Narcotic Drugs and Psychotropic Substances Act of 1985 in India. It provides definitions of key terms like cannabis, opium, and manufactured drugs. It outlines the objectives of the act to consolidate laws around narcotics and prevent illicit trafficking. Authorities and officers responsible for enforcement are mentioned, along with offenses and penalties. The document also discusses amendments to the act in 1988, 2001, and 2014. Rules related to schedules of narcotic and psychotropic substances are provided.
These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Kat...rightmanforbloodline
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TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
TEST BANK For Basic and Clinical Pharmacology, 14th Edition by Bertram G. Katzung, Verified Chapters 1 - 66, Complete Newest Version.
Integrating Ayurveda into Parkinson’s Management: A Holistic ApproachAyurveda ForAll
Explore the benefits of combining Ayurveda with conventional Parkinson's treatments. Learn how a holistic approach can manage symptoms, enhance well-being, and balance body energies. Discover the steps to safely integrate Ayurvedic practices into your Parkinson’s care plan, including expert guidance on diet, herbal remedies, and lifestyle modifications.
8 Surprising Reasons To Meditate 40 Minutes A Day That Can Change Your Life.pptxHolistified Wellness
We’re talking about Vedic Meditation, a form of meditation that has been around for at least 5,000 years. Back then, the people who lived in the Indus Valley, now known as India and Pakistan, practised meditation as a fundamental part of daily life. This knowledge that has given us yoga and Ayurveda, was known as Veda, hence the name Vedic. And though there are some written records, the practice has been passed down verbally from generation to generation.
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Muktapishti is a traditional Ayurvedic preparation made from Shoditha Mukta (Purified Pearl), is believed to help regulate thyroid function and reduce symptoms of hyperthyroidism due to its cooling and balancing properties. Clinical evidence on its efficacy remains limited, necessitating further research to validate its therapeutic benefits.
share - Lions, tigers, AI and health misinformation, oh my!.pptxTina Purnat
• Pitfalls and pivots needed to use AI effectively in public health
• Evidence-based strategies to address health misinformation effectively
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A proprietary approach developed by bringing together the best of learning theories from Psychology, design principles from the world of visualization, and pedagogical methods from over a decade of training experience, that enables you to: Learn better, faster!
TEST BANK For An Introduction to Brain and Behavior, 7th Edition by Bryan Kol...rightmanforbloodline
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TEST BANK For An Introduction to Brain and Behavior, 7th Edition by Bryan Kolb, Ian Q. Whishaw, Verified Chapters 1 - 16, Complete Newest Version
3. • Introduction
Alcohol is an important solvent excellent preservative and therapeutic agent but it is misused and it could
be a drug of addiction
Alcohol obtained at lower rate of duty may be misused for drinking purpose and hence it is necessary to
control the issue and transport of alcohol
In the absence of uniform excise policy, the price structure of alcohol containing medicine was varying
from state to state within country. In order to overcome this difficulty and to ensure uniform structure of
excise duty for alcohol product this act is passed.
These act providing legal binding on use of alcohol.
This act is effectively implement in India from 15 april,1957
Act has 11 chapter and 21 section.
4. • OBJECTIVE
This act provide levy and collection of duties of excise on medicinal and toilet preparation
containing alcohol, opium, Indian hemp, or other narcotic drugs.
To provide rules and provision to cover all types of preparation containing alcohol and
narcotic drugs.
5. • DEFINATIONS
Definitions comes under the act
Alcohol- alcohol means ethyl alcohol of any strength and purity having chemical
composition C2H5OH
Dutiable goods- it includes the medicinal and toilet preparation specified in the schedule as
being subject to duties of excise levied under this act.
Medicinal preparation- it includes the drugs used as remedy or prescription prepared for
internal or external use of human beings or animals.
6. Continue..
Bonded manufactory :means the premises or any part of the premises approved and licensed
for the manufacture and storage of medicinal and toilet preparations containing alcohol, opium,
Indian hemp and other narcotic drugs or narcotics on which duty has not been paid;
Non bonded manufactory; means the premises or any part of the premises approved and
licensed for the manufacture and storage of medicinal and toilet preparations containing
alcohol, opium Indian hemp and other narcotic drugs or narcotics on which duty has been paid;
Denatured spirit or denatured alcohol: means alcohol of any strength which has been rendered
unfit for human consumption by the addition of substances approved by the Central
Government
7. Continue..
spirit store- means that portion of the bonded or non-bonded manufactory which is set apart
for the storages of alcohol opium, Indian hemp and other narcotic drugs or narcotic purchased
free of duty or at prescribed rates of duty specified in the schedule to the Act;
Restricted preparation: these are medicinal preparation which are considered as capable of
being misused as ordinary alcohol beverages.
Unrestricted preparation; these are medicinal preparation which are considered to be not
capable of being misused as ordinary alcohol beverages.
Substandard preparation; it includes,
The pharmacopeia preparation in which amount of any of the various ingredient is below the
minimum.
8. • manufacture
There are 2 modes of manufacture of medicinal and toilet preparation
containing alcohol,
Manufacture in bond( use alcohol on which duty has not been paid)
Manufacture outside bond( use alcohol on which duty has been already paid)
It covers manufacturing of homeopathic, unani, and ayurvedic preparation
containing alcohol.
9. licensing
Central government give notification in official gazette, they provide it at
specific date,
no person shall engage in the production or manufacture of any dutiable goods
or other ingredient except under the authority and in accordance with the
terms and in accordance with the terms and conditions of license under this act.
Every license shall be granted for specific area with the conditions and
restrictions.
10. • Conditions of license
The license for alcoholic medicinal is given only when it is issued under drug and
cosmetic act ( DCA) and permission is taken by excise commissioner if the
formulation containing alcohol are being manufactured.
The license on payment of specified fee can be obtained under particular
conditions for manufacture in bond and outside bond of medicinal and toilet
preparation, ayurvedic, homeopathic, unani medicine .
11. • Procedure for license
A. Manufacture in bond : from the excise commissioner
B. Manufacture outside bond: from the state government authorised officer.
1. The application of grant of license submit in prescribed manner with fee
2. And reach to licensing authority at least 2 months before the proposed date of
manufacture.
12. • Details in application:
1. Name and address of applicant
2. If application is firm then name and address of partner.
3. If application is for company then name and address of directors, managers, and managing agents and
registration no. of company.
4. Name and address of place and site of bonded / non bonded manufactory.
5. Amount of capital proposed to be invested.
6. Number and full description of vats, stills and other apparatus and machinery which the applicant
wishes to set up.
7. Approximate date of starting production.
13. Continue..
8. In case of bonded laboratory : statement is necessary indicating that excise officer required full
time or part time.
9. The kind and no. of license held by applicant as per DCA.
10. In case of firm, true copy of partnership deed.
11. In case of company, list of directors, managers, copies of memorandum of association and latest
balance sheet.
12. A list of all preparation, that the license proposes to manufacture showing,
13. % or proportion of alcohol in preparation containing alcohol
14. The quantity of opium, Indian hemp, or other narcotic drugs in terms of weight in preparation
containing these substance.
14. • Enquiries by licensing authorities
1. Qualification and experience of the technical persons.
2. The equipment in bonded/ non bonded laboratory.
3. Suitability of the proposed building for the establishment of a laboratory.
After satisfying that the applicant is eligible for the issue of licence, the licensing
authorities shall issue a licence and approve plan of building is submitted along with the
application.
15. • bonded manufactory or manufacture in bond
Without payment of duty, rectified spirit is issued with sufficient security and bond.
Bonded laboratory ideal requirement.
1. Spirit store
2. Room for manufacturing of medicinal preparation
3. Rooms for storage of finished preparation
4. Room for manufacturing and storage of toilet preparation.
5. Every room in bonded laboratory should bear a board indicating the room and serial
number.
16. Continue..
6. Sinks and wash basin connected to the general drainage of laboratory
7. Gas and electric supply should be arranged so that they can be easily cut at end of the day.
8. Windows of the bonded lab should be made up of iron rods of prescribed dimension and
should covered inside with strong wire netting.
9. Only one entrance to bonded laboratory and one door to each of the compartment.
10. All the doors are secured with excise ticket locks in the absence of officer in charge.
11. No alteration in the bonded premises shall be made without excise commissioner permission.
12. All the vessels containing medicinal and toilet preparation on which duty has not been paid
should bear excise ticket locks.
17. Continue..
I. Obtaining the rectified spirit from warehouse
II. Verification and storage of spirit received
III. Issue of rectified spirit from store to manufacturer
IV. Storage of finished products
V. Issue of preparation from bonded lab
18. • Non bonded laboratory:
Manufacture and sale should be conducted between sunrise and sunset only
And only on those days and hours which is fixed by excise commissioner.
1. building arrangement
2. Obtaining the rectified spirit duty paid
3. Manufacture and storage of preparation.
19. 1.Buliding arrangement
1. Separate facility for spirit store, laboratory, and finished goods.
2. One entrance to each department
3. All the pipes from sinks and wash basins inside the laboratory should be connected with general
drainage
4. Arrangement of gas and electric supply should be connected with general drainage.
5. Separate spirit store for spirit purchased at different rates of duty.
20. 2.Obtaning the Rectified Spirit Duty Paid
1. Licensee should send the indent along with treasury challan ( evidence of duty payable) to the
officer in-charge of distillery.
2. The cost of such rectified spirit shall be paid by the licensee to the distillery.
3. After confirmation about correct amount is paid, officer incharge of distillery, order the issue
of rectified spirit required along with the permit covering the issue.
4. After making entry in proper register, obtained spirit transferred to the spirit store.
21. 3. Manufacture and storage of preparation
1. Manufacturing should be carried out in licensed premises only.
2. Registered each manufacturing preparation along with its batch.
3. Transferred finished preparation to the finished store and arrange so that they
can easily be checked from account register.
4. Finished product prepared from alcohol with different duties need to be stored
separately.
5. Bulk preparation should be transferred into the vessel of 28 ml capacity and
sealed.
22. • Exemption from duty
1. Government hospitals and dispensary
2. Charitable hospitals and dispensaries
3. Government medical stores
4. Institution certified by district medical officer supplying medicine free to poor.
5. Anything in public interest.
23. Classification of medicinal and toilet preparation
containing alcohol
Allopathic preparation homeopathic preparation Ayurveda preparation
Official preparation are made
according to official books
formulae like IP, BP,BPC, USP, NF
American, British and general
pharmacopoeia are used as
standard for this preparation.
1.Self generated alcohol containing
substance:
Ex. Asavas and arista's
2.sub.preapared by distillation or to which
alcohol is added at any stage of
manufacture.
Non official preparation are
made according to allopathic
system
24. Export of medicinal and toilet preparation ( alcoholic
preparation)
No duty shall be paid on alcoholic preparation which are exported from India.
It is of 2 types:
Export of duty paid goods (non bonded) under claim of rebate of duty
Export of non- duty paid goods.(under bond)
25. 1.Export of Duty Paid Goods
1. Should be export under claim of rebate of duty
2. Minimum 48 hours notice to be given to excise officer
3. Manufacturer should present the consignment to be exported to the concerning officer who send that
samples to the chemical examiner for analysis.
4. chemical examiner gives the report in duplicate
5. Based on alcoholic content excise duty rebated.
26. Continue.
The officer incharge verify the application for following details
1. Name and address of consignee
2. Total quantity of goods packed
3. Description of the goods
4. Gross weight of each package
After verifying the application the officer incharge:
1. Seal each pack with his official seal
2. Returns duplicate copy to consigner
3. On arrival of the goods at place of export, should be presented to customs collector for examination with
application
27. 2.Export of non duty paid goods:
1. The exporter should present an application in triplicate to excise officer in charge of the bonded laboratory
2. Mention the way of transport (by sea / air/ by parcel post)
3. Package should be marked with inks with particular serial number, owners names, alcoholic strength.
4. Officer incharge verify the application for details provided
5. Seal all packages with his official seal.
6. Then the packages then exported by same way as that of duty paid goods.
28. Power of excise officer:
Inspection
Entry, search and seizure
Detention of person
Notices
Disposal of seized articles/ arrested persons
Power of arrest
Power of make rules
29. Duties of excise officer
1. Checking the qualification and experience of technical staff, equipment, suitability of building and applicants
financial position.
2. Visit premises at regular interval's
Responsibility of excise officer
1. Correct collection of duty and penalty
2. Articles seized should be disposed speedily
3. Persons arrested should be forwarded without delay to excise officer
30. Offences and penalties
Offences Penalties
By licensee
Contravention of any of the provision
Failure to pay any duty of excise payable under this act
Failure to supply required information
Imprisonment: 6 month or fine rs.2000/- or both
Failure to furnish proof of export fine rs.2000/- extent to twice the amount of duty
Obstruction to the officer from performing his duty fine rs.500/-
Maintaining false accounts of stocks fine rs.2000/-
Illegal sale of dutiable goods fine rs.1000/-
Warehousing related offences Fine up to 2000/-
31. Offences and penalties
offences penalties
By excise officer
Discloser of information Fine up to 1000/-
Refusal to perform duties Imprisonment up to 3 months or fine up
to 3 month pay