Prefilled nontherapeutic nicotine device definition

Prefilled nontherapeutic nicotine device means the same as that term is defined in Section 76-10-101.
Prefilled nontherapeutic nicotine device means a nontherapeutic nicotine device that is sold prefilled with a nontherapeutic nicotine device substance.
Prefilled nontherapeutic nicotine device means the same as that term is defined 1358 in Section 76-10-101. 1359 [(11)] (22) "Retailer" means a person that: 1360 (a) sells or distributes a cigarette, an electronic cigarette product, or a nicotine product 1361 to a consumer in the state; or 1362 (b) intends to sell or distribute a cigarette, an electronic cigarette product, or a nicotine 1363 product to a consumer in the state. 1364 [(12)] (23) "Stamp" means the indicia required to be placed on a cigarette package that 1365 evidences payment of the tax on cigarettes required by Section 59-14-205. 1366 [(13)] (24) (a) "Tobacco product" means a product made of, or containing, tobacco. 1367 (b) "Tobacco product" includes: 1368 (i) a cigarette produced from a cigarette rolling machine; 1369 (ii) a little cigar; or 1370 (iii) moist snuff. 1371 (c) "Tobacco product" does not include a cigarette. 1372 [(14)] (25) "Tribal lands" means land held by the United States in trust for a federally 1373 recognized Indian tribe. 1374 Section 28. Section 59-14-104 is enacted to read: 1375 59-14-104. Rate reduction for modified risk tobacco products. 1376 (1) Beginning July 1, 2021, the tax imposed under this chapter is reduced in 1377 accordance with Subsection (2): 1378 (a) on the first day of a calendar quarter; and 1379 (b) after a 90-day period beginning on the day on which the commission receives a 1380 notice from the manufacturer of a product that has received a modified risk tobacco product 1381 order from the United States Food and Drug Administration. 1382 (2) The tax imposed under this chapter is reduced by: 1383 (a) 50% for any product that is issued a modified risk tobacco product order under 21 1384 U.S.C. Sec. 387k(g)(1); and 1385 (b) 25% for any product that is issued a modified risk tobacco product order under 21 1386 U.S.C. Sec. 387k(g)(2). 1387 Section 29. Section 59-14-302 is amended to read:

More Definitions of Prefilled nontherapeutic nicotine device

Prefilled nontherapeutic nicotine device means the same as that term is defined
Prefilled nontherapeutic nicotine device means {a nontherapeutic nicotine device that is sold prefilled with a nontherapeutic nicotine device substance}the same as that term is defined in Section 76-10-101.

Related to Prefilled nontherapeutic nicotine device

  • Nicotine product means a product that contains nicotine and is not any of the following:

  • Biological Samples means any physical samples obtained from Study Participants in accordance with the Protocol for the purposes of the Study.

  • Marihuana-infused product means a topical formulation, tincture, beverage, edible substance, or similar product containing marihuana and other ingredients and that is intended for human consumption.

  • Aerosol coating product means a pressurized coating product containing pigments or resins that dispenses product ingredients by means of a propellant, and is packaged in a disposable can for hand-held application, or for use in specialized equipment for ground traffic/marking applications.

  • Biological product means a virus, therapeutic serum, toxin, antitoxin, vaccine, blood, blood component or derivative, allergenic product, protein other than a chemically synthesized polypeptide, or analogous product, or arsphenamine or any derivative of arsphenamine or any other trivalent organic arsenic compound, applicable to the prevention, treatment, or cure of a disease or condition of human beings.

  • Diagnostic Product means In Vitro Diagnostics, In Vivo Diagnostic Agents and any product used for Diagnosis.

  • Anti-Static Product means a product that is labeled to eliminate, prevent, or inhibit the accumulation of static electricity. “Anti-Static Product” does not include “Electronic Cleaner,” “Floor Polish or Wax,” “Floor Coating,” and products that meet the definition of “Aerosol Coating Product” or “Architectural Coating.”

  • Edible cannabis product means cannabis product that is intended to be used, in whole or in part, for human consumption, including, but not limited to, chewing gum, but excluding products set forth in Division 15 (commencing with Section 32501) of the Food and Agricultural Code. An edible cannabis product is not considered food, as defined by Section 109935 of the Health and Safety Code, or a drug, as defined by Section 109925 of the Health and Safety Code.

  • Spray buff product means a product designed to restore a worn floor finish in conjunction with a floor buffing machine and special pad.

  • Therapeutic diet means meals served that are soft, low-fat, low-sodium or controlled calorie.

  • Marijuana-infused products means products that contain marijuana or marijuana extracts and are intended for human use. The term "marijuana-infused products" does not include useable marijuana.

  • Alternative nicotine product means any vaping product, whether or not it includes nicotine, including electronic smoking devices, that can be ingested into the body by chewing, smoking, absorbing, dissolving, inhaling, or by any other means. ‘Alternative nicotine product’ does not include:

  • Combination Product means (a) a product containing a Licensed Product together with one or more other active ingredients that have independent biologic or chemical activity when present alone that are sold as a single unit, or (b) a Licensed Product together with one or more products, devices, pieces of equipment or components thereof, that are sold as a single package at a single price.

  • Aerosol product means a pressurized spray system that dispenses product ingredients by means of a propellant contained in a product or a product's container, or by means of a mechanically induced force. “Aerosol Product” does not include “Pump Spray.”

  • Orthotic device means a custom-fitted or custom-fabricated medical device that is applied to a part of the human body to correct a deformity, improve function, or relieve symptoms of a disease.

  • Product means any deliverable under the Contract, which may include commodities, services, technology or software.

  • Recycled product means a product containing recovered material, or post-consumer recovered material, or both.

  • medicinal product means any substance or combination of substances presented for treating or preventing disease in human beings or animals and any substance or combination of substances which may be administered to human beings or animals with a view to making a medical diagnosis or to restoring, correcting or modifying physiological functions in humans or in animals;

  • Cannabis product means cannabis that has undergone a process whereby the plant material has been transformed into a concentrate, including, but not limited to, concentrated cannabis, or an edible or topical product containing cannabis or concentrated cannabis and other ingredients.

  • Reference biological product means the single biological product licensed pursuant to 42 U.S.C.

  • Fluoroscopic imaging assembly means a subsystem in which X-ray photons produce a visual image. It includes the image receptor(s) such as the image intensifier and spot-film device, electrical interlocks, if any, and structural material providing linkage between the image receptor and diagnostic source assembly.

  • Tobacco product means any substance containing tobacco leaf, including but not limited to, cigarettes, cigars, pipe tobacco, hookah tobacco, snuff, chewing tobacco, dipping tobacco, bidis, blunts, clove cigarettes, or any other preparation of tobacco; and any product or formulation of matter containing biologically active amounts of nicotine that is manufactured, sold, offered for sale, or otherwise distributed with the expectation that the product or matter will be introduced into the human body by inhalation; but does not include any cessation product specifically approved by the U.S. Food and Drug Administration for use in treating nicotine or tobacco dependence.

  • Active Pharmaceutical Ingredient or “API” shall mean one or more of the following active pharmaceutical ingredients: tenofovir alafenamide (“TAF”), tenofovir disoproxil fumarate (“TDF”), elvitegravir (“EVG”), and cobicistat (“COBI”).

  • Vapor product means any:

  • Marijuana product means marijuana as defined in 50-32-101 and marijuana-infused products

  • Therapeutically equivalent drug products means drug products that contain the same active ingredients and are identical in strength or concentration, dosage form, and route of administration and that are classified as being therapeutically equivalent by the U.S. Food and Drug Administration pursuant to the definition of "therapeutically equivalent drug products" set forth in the most recent edition of the Approved Drug Products with Therapeutic Equivalence Evaluations, otherwise known as the "Orange Book."