6-12A-3
stamping agent, or distributor shall have 30 days from receipt of notice from the department
regarding the change in the directory to sell the brand family that is delisted. No delisted
brand family may be sold after the 30 day period. (4) Every wholesaler and distributor shall
provide and update as necessary an electronic mail address to the commissioner for the purpose
of receiving any notifications as may be required by this chapter. (c) Prohibition against
stamping, sale, or import of cigarettes not in the directory. It shall be unlawful for any
person to do either of the following: (1) Affix a stamp to a package or other container of
cigarettes of a tobacco product manufacturer or brand family not included in the directory.
(2) Sell, offer, or possess for sale in this state, or import for personal consumption
in this state, cigarettes of a tobacco product manufacturer or brand family not included in
the directory. (Act 2003-372, p. 1049, §2; Act 2014-341, p. 1266, §1.)...
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2-26-2
Section 2-26-2 Powers and duties of commissioner generally. It shall be the duty of the Commissioner
of Agriculture and Industries, who may act individually or through his authorized agents to:
(1) Inspect, sample, make analyses of and test agricultural, vegetable, herb, tree, shrub
and flower seeds transported, sold, offered or exposed for sale or distributed within this
state for sowing or planting purposes, at such time and place and to such extent as he may
deem necessary to determine whether said seeds are in compliance with the provisions of this
article and notify promptly the person who transported, sold, offered or exposed the seed
for sale of any violation; (2) Enter upon any public or private premises during regular business
hours in order to have access to seeds subject to this article and the rules and regulations
thereunder; (3) Issue and enforce a written or printed "stop-sale," "suspension
from sale" or "nonuse" order to the owner or custodian of any lot of...
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22-6-122
Section 22-6-122 Medicaid Pharmacy and Therapeutics Committee - Classification and recommendation
of drugs; assurance of quality patient care; review of pharmaceutical products. (a) The Medicaid
Pharmacy and Therapeutics Committee shall review and recommend classes of drugs to the Medicaid
Commissioner for inclusion in the Medicaid Preferred Drug Plan. Class means a therapeutic
group of pharmaceutical agents approved by the FDA as defined by the American Hospital Formulary
Service. The classes of anti-retroviral and anti-psychotic drugs shall not be included in
the Medicaid Preferred Drug Plan. (b) The Medicaid Pharmacy and Therapeutics Committee shall
develop its preferred drug list recommendations by considering the clinical efficacy, safety,
and cost effectiveness of a product. Within each covered class, the committee shall review
and recommend drugs to the Medicaid Commissioner for inclusion on a preferred drug list. Generics
and over the counter drugs covered by Medicaid may be...
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8-17-82
Section 8-17-82 Labeling requirement. (a) Each person selling, offering for sale, storing or
using in the state any petroleum product must label, or cause to be labeled, each tank car,
tank, barrel, pump, or other container in which such petroleum product is contained or marketed
with the words "guaranteed legal standards" and with an additional word or words
denoting the precise character of the petroleum product in the container so labeled. Each
word in such label shall be legibly printed in letters not less than one-half inch in height.
(b) An alternate manner for container and other labeling information as required under subsection
(a) of this section may be prescribed by the Board of Agriculture and Industries pursuant
to rules and regulations which shall be consistent with the evident intent and purposes of
this section. (c) In addition to the requirements of subsections (a) and (b) of this section
each person selling, offering for sale, storing or using in the state any...
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8-33-7
Section 8-33-7 Form and contents of warranty. (a) Every vehicle protection product warranty
in its entirety shall be written, printed, or typed in eight point type size or larger and
shall not be sold or offered for sale in this state unless the warranty: (1) States that the
obligations of the warrantor to the warranty holder are guaranteed under a warranty reimbursement
insurance policy if the warrantor elects to meet its financial responsibility obligations
under subsection (b) of Section 8-33-5 or states that the obligations of the warrantor under
the warranty are backed by the full faith and credit of the warrantor if the warrantor elects
to meet its financial responsibility obligations under subsection (c) of Section 8-33-5. (2)
States that in the event a warranty holder must make a claim against a party other than the
warranty reimbursement insurance policy issuer, the warranty holder is entitled to make a
direct claim against the insurer upon the failure of the warrantor to pay...
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16-25A-18
Section 16-25A-18 Generic equivalent medications. As a condition of participation in the Public
Education Employees Health Insurance Programs (PEEHIP), a pharmacist shall dispense a generic
equivalent medication to fill a prescription for a patient covered by PEEHIP when one is available
unless the physician indicates in longhand writing on the prescription, indicates by mark
or signature in the appropriate place on the prescription, or indicates in an electronic prescription,
the following: "medically necessary" or "dispense as written" or "do
not substitute". The generic equivalent drug product dispensed shall be pharmaceutically
and therapeutically equivalent and contain the same active ingredient or ingredients, and
shall be of the same dosage, form, and strength. (Act 2002-266, p. 549, §1; Act 2016-304,
§1.)...
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20-1-51
Section 20-1-51 When cosmetics deemed adulterated. (a) A cosmetic shall be deemed adulterated:
(1) If it bears or contains any poisonous or deleterious substance which may render it injurious
to users under the conditions of use prescribed in the labeling thereof or under such conditions
of use as are customary and usual; (2) If it consists in whole or in part of any filthy, putrid,
or decomposed substance; (3) If it has been prepared, packed, or held under unsanitary conditions
whereby it may have become contaminated with filth or rendered injurious to health; (4) If
its container is composed in whole or in part of any poisonous or deleterious substance which
may render the contents injurious to health; or (5) If it is not a hair dye and it bears or
contains a coal-tar color other than one from a batch that has been certified in accordance
with regulations promulgated under the federal Food, Drug and Cosmetic Act. (b) The provisions
of subdivision (1) of subsection (a) of this section...
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22-20-11
Section 22-20-11 Restrictions on retail sales of certain poisons. (a) It shall be unlawful
for any person to retail any poisons enumerated in Schedules "A" and "B"
which are as follows, except upon the conditions named in this section: (1) Schedule "A"
- biniodide of mercury, cyanide of potassium, carbolic acid, hydrocyanic acid, strychnine,
arsenate and its preparations and all other poisonous alkaloids and their salts and the essential
oil of bitter almonds. (2) Schedule "B" - acenite, belladonna, colchium, conium,
nux vomica, henbane, savin, ergot, cotton root, cantharides, creosote, veratrium, digitalis
and their pharmaceutical preparations, croton oil, chloroform, sulphate of zinc, corrosive
sublimate, red precipitate, white precipitate, mineral acids and oxalic acid. (b) Any of the
poisons included in Schedule "A" may be legally sold by any registered pharmacist,
but he shall, before delivering the same to the purchaser, cause an entry to be made in a
book kept for that purpose,...
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36-29-18
Section 36-29-18 Generic equivalent medications. As a condition of participation in an insurance
policy of the State Employees Insurance Board (SEIB) a pharmacist shall dispense a generic
equivalent medication to fill a prescription for a patient covered by SEIB when one is available
unless the physician indicates in longhand writing on the prescription "medically Necessary"
or "dispense as written" or "do not substitute". The generic equivalent
drug product dispensed shall be pharmaceutically and therapeutically equivalent and contain
the same active ingredient, or ingredients, and shall be of the same dosage, form, and strength.
(Act 2002-266, p. 549, §1.)...
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20-1-22
Section 20-1-22 When articles deemed adulterated - Food generally. An article shall be deemed
adulterated in the case of food: (1) If any substance has been mixed and packed with it so
as to reduce or lower or injuriously affect its quality or strength; (2) If any substance
has been substituted wholly or in part for the article; (3) If any valuable constituent of
the article has been wholly or in part abstracted; (4) If it is mixed, colored, powdered,
coated, stained, or otherwise treated in a manner whereby damage or inferiority is concealed
or in a manner whereby the appearance of said article is improved; provided, that this subdivision
shall not apply to the precoloring or processing of fruits where such precoloring or processing
does not conceal damage or inferiority; (5) If it contains any poisonous or deleterious ingredient
which may render such article injurious to health; (6) If it consists in whole or in part
of a filthy, decomposed, or putrid animal or vegetable substance or...
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