32A-6-302 (Repealed 07/01/11) - Operational restrictions. - Utah Statutes

State Codes and Statutes

Statutes > Utah > Title-32a > Chapter-06 > 32a-6-302-repealed-07-01-11

32A-6-302 (Repealed 07/01/11). Operational restrictions.
In addition to the restrictions, conditions, and requirements of Section 32A-6-105, eachindustrial or manufacturing use permit is subject to the following operating restrictions:
(1) An industrial or manufacturer permittee may produce for lawful use and sale thefollowing:
(a) vinegar;
(b) preserved nonintoxicating cider;
(c) food preparations;
(d) a United States Pharmacopoeia or national formulary preparation in conformity withTitle 58, Chapters 17b, 37, 37a, 37b, and 37c, if the preparation:
(i) conforms to standards established by:
(A) the Department of Agriculture and Food; and
(B) the Department of Health; and
(ii) contains no more alcohol than is necessary to preserve or extract the medicinal,flavoring, or perfumed properties of the treated substances; and
(e) wood and denatured alcohol if manufactured in compliance with the formulas andregulations under Title 27, Code of Federal Regulations, Parts 19, 20, and 21.
(2) (a) An industrial or manufacturer permittee that produces patent or proprietarymedicines containing alcohol may sell the medicines in the original and unbroken package if themedicine contains sufficient medication to prevent its use as an alcoholic beverage.
(b) An industrial or manufacturer permittee described in this Subsection (2) shall, uponrequest by the department, provide a sufficient sample of the medicine to enable the departmentto have the medicine analyzed for purposes of this section.

Repealed by Chapter 276, 2010 General Session
Amended by Chapter 284, 2007 General Session

State Codes and Statutes

Statutes > Utah > Title-32a > Chapter-06 > 32a-6-302-repealed-07-01-11

32A-6-302 (Repealed 07/01/11). Operational restrictions.
In addition to the restrictions, conditions, and requirements of Section 32A-6-105, eachindustrial or manufacturing use permit is subject to the following operating restrictions:
(1) An industrial or manufacturer permittee may produce for lawful use and sale thefollowing:
(a) vinegar;
(b) preserved nonintoxicating cider;
(c) food preparations;
(d) a United States Pharmacopoeia or national formulary preparation in conformity withTitle 58, Chapters 17b, 37, 37a, 37b, and 37c, if the preparation:
(i) conforms to standards established by:
(A) the Department of Agriculture and Food; and
(B) the Department of Health; and
(ii) contains no more alcohol than is necessary to preserve or extract the medicinal,flavoring, or perfumed properties of the treated substances; and
(e) wood and denatured alcohol if manufactured in compliance with the formulas andregulations under Title 27, Code of Federal Regulations, Parts 19, 20, and 21.
(2) (a) An industrial or manufacturer permittee that produces patent or proprietarymedicines containing alcohol may sell the medicines in the original and unbroken package if themedicine contains sufficient medication to prevent its use as an alcoholic beverage.
(b) An industrial or manufacturer permittee described in this Subsection (2) shall, uponrequest by the department, provide a sufficient sample of the medicine to enable the departmentto have the medicine analyzed for purposes of this section.

Repealed by Chapter 276, 2010 General Session
Amended by Chapter 284, 2007 General Session

State Codes and Statutes

Back To Homepage

State Codes and Statutes

Statutes > Utah > Title-32a > Chapter-06 > 32a-6-302-repealed-07-01-11

32A-6-302 (Repealed 07/01/11). Operational restrictions.
In addition to the restrictions, conditions, and requirements of Section 32A-6-105, eachindustrial or manufacturing use permit is subject to the following operating restrictions:
(1) An industrial or manufacturer permittee may produce for lawful use and sale thefollowing:
(a) vinegar;
(b) preserved nonintoxicating cider;
(c) food preparations;
(d) a United States Pharmacopoeia or national formulary preparation in conformity withTitle 58, Chapters 17b, 37, 37a, 37b, and 37c, if the preparation:
(i) conforms to standards established by:
(A) the Department of Agriculture and Food; and
(B) the Department of Health; and
(ii) contains no more alcohol than is necessary to preserve or extract the medicinal,flavoring, or perfumed properties of the treated substances; and
(e) wood and denatured alcohol if manufactured in compliance with the formulas andregulations under Title 27, Code of Federal Regulations, Parts 19, 20, and 21.
(2) (a) An industrial or manufacturer permittee that produces patent or proprietarymedicines containing alcohol may sell the medicines in the original and unbroken package if themedicine contains sufficient medication to prevent its use as an alcoholic beverage.
(b) An industrial or manufacturer permittee described in this Subsection (2) shall, uponrequest by the department, provide a sufficient sample of the medicine to enable the departmentto have the medicine analyzed for purposes of this section.

Repealed by Chapter 276, 2010 General Session
Amended by Chapter 284, 2007 General Session