Nrs: Chapter 585 - Food, Drugs And Cosmetics: Adulteration; Labels; Brands

Link to law: https://www.leg.state.nv.us/NRS/NRS-585.html
Published: 2015

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[Rev. 2/11/2015 11:28:55

AM--2014R2]

CHAPTER 585 - FOOD, DRUGS AND COSMETICS:

ADULTERATION; LABELS; BRANDS

GENERAL PROVISIONS

NRS 585.010           Short

title.

NRS 585.020           Definitions.

NRS 585.030           “Advertisement”

defined.

NRS 585.040           “Commissioner”

defined.

NRS 585.050           “Contaminated

with filth” defined.

NRS 585.060           “Cosmetic”

defined.

NRS 585.070           “Device”

defined.

NRS 585.080           “Drug”

defined.

NRS 585.090           “Federal

Act” defined.

NRS 585.100           “Food”

defined.

NRS 585.110           “Immediate

container” defined.

NRS 585.120           “Label”

defined.

NRS 585.130           “Labeling”

defined.

NRS 585.140           “New

drug” defined.

NRS 585.150           “Official

compendium” defined.

NRS 585.170           Factors

to be considered in determining whether label or advertisement is misleading.

NRS 585.180           Construction

of representation that drug is antiseptic.

NRS 585.190           Scope

of provisions regulating sales.

ADMINISTRATION

NRS 585.200           Appointment

of Commissioner of Food and Drugs.

NRS 585.210           Regulations.

NRS 585.220           Hearings.

NRS 585.230           Record

of adulterated, mislabeled or misbranded foods, drugs, devices and cosmetics;

biennial report of Commissioner; dissemination of information.

NRS 585.240           Inspection

of factories and vehicles: Purposes; examination of samples.

NRS 585.245           Licensing

of persons manufacturing, compounding, processing or packaging drugs, devices

or cosmetics: Regulations; fees; inspection.

NRS 585.250           Tagging

of articles believed to be dangerous to health: Contents of tag; unlawful

sales.

NRS 585.260           Removal

of tag or marking from detained or quarantined article; liability of person

removing tag or other marking.

NRS 585.270           Petition

for condemnation and destruction of adulterated or misbranded article.

NRS 585.280           Destruction

of article found to be adulterated or misbranded.

NRS 585.290           Correction

of defect by proper labeling or processing.

FOOD

NRS 585.300           Adulterated

food: Poisonous or insanitary ingredients.

NRS 585.310           Adulterated

food: Absence, substitution or addition of constituents.

NRS 585.320           Adulterated

food: Standards of purity, quality or strength.

NRS 585.330           Adulterated

food: Confectionery containing nonnutritive substance.

NRS 585.350           Misbranded

food.

NRS 585.355           Use

of “honey” in product label or designation restricted; “honey” defined.

NRS 585.360           Food

containing filthy, decomposed or putrid substance declared nuisance;

condemnation or destruction by Commissioner.

DRUGS AND DEVICES

NRS 585.370           Adulterated

drugs and devices: Poisonous or insanitary ingredients.

NRS 585.380           Adulterated

drugs and devices: Strength, quality or purity differing from official

compendium.

NRS 585.390           Adulterated

drugs and devices: Misrepresentation of strength, quality or purity if drug not

in compendium.

NRS 585.400           Adulterated

drugs and devices: Mixture with or substitution of another substance.

NRS 585.410           Misbranded

drugs and devices: False or misleading label.

NRS 585.420           Misbranded

drugs and devices: Contents of label on package.

NRS 585.430           Misbranded

drugs and devices: Habit-forming substances.

NRS 585.440           Misbranded

drugs and devices: Designation of drug by name not in compendium.

NRS 585.450           Misbranded

drugs and devices: Directions for use and warnings on label.

NRS 585.460           Misbranded

drugs and devices: Misleading container; imitation; offer for sale under

another name.

NRS 585.470           Misbranded

drugs and devices: Health-endangering when used as prescribed.

NRS 585.480           Misbranded

drugs and devices: Drug containing amidopyrine, barbituric acid, cinchophen,

dinitrophenol or sulfanilamide sold without prescription.

NRS 585.485           Restrictions

on sale of dimethyl sulfoxide; penalty.

NRS 585.490           Introduction

or delivery for introduction of new drug into intrastate commerce before

application is effective prohibited.

NRS 585.495           Licensing

of manufacture of amygdalin and procaine hydrochloride; duties and powers of

Commissioner; injunctive relief.

NRS 585.497           Assessment

on gross receipts from sale of amygdalin and procaine hydrochloride.

COSMETICS

NRS 585.500           Adulterated

cosmetics.

NRS 585.510           Misbranded

cosmetics.

PROHIBITED ACTS AND PENALTIES

NRS 585.520           Prohibited

acts.

NRS 585.530           When

advertisement deemed false.

NRS 585.535           Unlawful

to sell or offer to sell beverage container opened by detaching metal ring or

tab; exceptions; penalty.

NRS 585.540           Duties

of Attorney General and district attorneys; hearing by Commissioner before

institution of criminal proceedings.

NRS 585.550           Penalties.

_________

_________

 

GENERAL PROVISIONS

      NRS 585.010  Short title.  This

chapter may be cited as the Nevada Food, Drug and Cosmetic Act.

      [1:177:1939; 1931 NCL § 6206]

      NRS 585.020  Definitions.  For

the purpose of this chapter, the words and terms defined in NRS 585.030 to 585.150,

inclusive, have the meanings ascribed to them in those sections.

      [Part 2:177:1939; 1931 NCL § 6206.01]—(NRS A 1985, 530)

      NRS 585.030  “Advertisement” defined.  “Advertisement”

means all representations disseminated in any manner or by any means, other

than by labeling, for the purpose of inducing, or which are likely to induce,

directly or indirectly, the purchase of food, drugs, devices or cosmetics.

      [Part 2:177:1939; 1931 NCL § 6206.01]

      NRS 585.040  “Commissioner” defined.  “Commissioner”

means the Commissioner of Food and Drugs.

      [Part 2:177:1939; 1931 NCL § 6206.01]

      NRS 585.050  “Contaminated with filth” defined.  “Contaminated

with filth” applies to any food, drug, device or cosmetic not securely

protected from dust, dirt and, as far as may be necessary by all reasonable

means, from all foreign or injurious contaminations.

      [Part 2:177:1939; 1931 NCL § 6206.01]

      NRS 585.060  “Cosmetic” defined.

      1.  “Cosmetic” means:

      (a) Articles intended to be rubbed, poured,

sprinkled or sprayed on, introduced into or otherwise applied to the human body

or any part thereof for cleansing, beautifying, promoting attractiveness or

altering the appearance, including wigs, hairpieces and postiches; and

      (b) Articles intended for use as a component of

any such articles.

      2.  “Cosmetic” shall not include soap.

      [Part 2:177:1939; 1931 NCL § 6206.01]—(NRS A 1969,

877)

      NRS 585.070  “Device” defined.  Except

when used in NRS 585.170, “device” means

instruments, apparatus and contrivances, including their components, parts and

accessories, intended:

      1.  For use in the diagnosis, cure,

mitigation, treatment or prevention of disease in humans or other animals; or

      2.  To affect the structure or any function

of the bodies of humans or other animals.

      [Part 2:177:1939; 1931 NCL § 6206.01]

      NRS 585.080  “Drug” defined.

      1.  “Drug” means:

      (a) Articles recognized in the official United

States Pharmacopoeia, official Homeopathic Pharmacopoeia of the United States

or official National Formulary, or any supplement to any of them;

      (b) Articles intended for use in the diagnosis,

cure, mitigation, treatment or prevention of disease in humans or other

animals;

      (c) Articles, other than food, intended to affect

the structure or any function of the bodies of humans or other animals; and

      (d) Articles intended for use as a component of

any article specified in paragraph (a), (b) or (c).

      2.  “Drug” does not include devices or

their components, parts or accessories.

      [Part 2:177:1939; 1931 NCL § 6206.01]

      NRS 585.090  “Federal Act” defined.  “Federal

Act” means the Federal Food, Drug, and Cosmetic Act, 21 U.S.C. §§ 301 et seq.,

as that act exists on June 30, 1983.

      [Part 2:177:1939; 1931 NCL § 6206.01]—(NRS A 1983, 189)

      NRS 585.100  “Food” defined.  “Food”

means:

      1.  Articles used for food or drink for

humans or other animals;

      2.  Chewing gum; and

      3.  Articles used for components of any

such article.

      [Part 2:177:1939; 1931 NCL § 6206.01]

      NRS 585.110  “Immediate container” defined.  “Immediate

container” does not include package liners.

      [Part 2:177:1939; 1931 NCL § 6206.01]

      NRS 585.120  “Label” defined.  “Label”

means a display of written, printed or graphic matter upon the immediate

container of any article; and a requirement made by or under authority of this

chapter that any word, statement or other information appear on the label shall

not be considered to be complied with unless such word, statement or other

information also appears on the outside container or wrapper, if there is any,

of the retail package of such article, or is easily legible through the outside

container or wrapper.

      [Part 2:177:1939; 1931 NCL § 6206.01]

      NRS 585.130  “Labeling” defined.  “Labeling”

means all labels and other written, printed or graphic matter:

      1.  Upon an article or any of its

containers or wrappers; or

      2.  Accompanying such article.

      [Part 2:177:1939; 1931 NCL § 6206.01]

      NRS 585.140  “New drug” defined.  “New

drug” means any drug the composition of which is such that the drug:

      1.  Is not generally recognized, among

experts qualified by scientific training and experience to evaluate the safety

and effectiveness of drugs, as safe and effective for use under the conditions

prescribed, recommended or suggested in the labeling thereof; or

      2.  As a result of investigations to

determine its safety and effectiveness for use under those conditions, has

become so recognized, but which has not, other than in the investigations, been

used to a material extent or for a material time under those conditions.

      [Part 2:177:1939; 1931 NCL § 6206.01]—(NRS A 1983, 189)

      NRS 585.150  “Official compendium” defined.  “Official

compendium” means the official United States Pharmacopoeia, official

Homeopathic Pharmacopoeia of the United States, official National Formulary or

any supplement to any of them.

      [Part 2:177:1939; 1931 NCL § 6206.01]

      NRS 585.170  Factors to be considered in determining whether label or

advertisement is misleading.  If an

article is alleged to be misbranded because the labeling is misleading, or if

an advertisement is alleged to be false because it is misleading, then, in

determining whether the labeling or advertisement is misleading, there shall be

taken into account, among other things, not only representations made or

suggested by statement, word, design, device, sound or in any combination

thereof, but also the extent to which the labeling or advertisement fails to

reveal facts material in the light of such representations or material with

respect to consequences which may result from the use of the article to which

the labeling or advertisement relates under the conditions of use prescribed in

the labeling or advertisement thereof or under such conditions of use as are

customary or usual.

      [Part 2:177:1939; 1931 NCL § 6206.01]

      NRS 585.180  Construction of representation that drug is antiseptic.  The representation of a drug, in its labeling

or advertisement, as an antiseptic shall be considered to be a representation

that it is a germicide, except in the case of a drug purporting to be, or

represented as, an antiseptic for inhibitory use as a wet dressing, ointment,

dusting powder, or such other use as involves prolonged contact with the body.

      [Part 2:177:1939; 1931 NCL § 6206.01]

      NRS 585.190  Scope of provisions regulating sales.

      1.  The provisions of this chapter

regarding the selling of foods, drugs, devices or cosmetics shall be considered

to include:

      (a) The manufacture, production, processing,

packing, exposure, offer, possession and holding of any such article for sale;

      (b) The sale, dispensing and giving of any such

article; and

      (c) The supplying or applying of any such

articles in the conduct of any food, drug or cosmetic establishment.

      2.  The provisions of this chapter do not

apply to the operation of any official establishment as defined in NRS 583.375.

      [Part 2:177:1939; 1931 NCL § 6206.01]—(NRS A 1969,

991)

ADMINISTRATION

      NRS 585.200  Appointment of Commissioner of Food and Drugs.  The Administrator of the Division of Public

and Behavioral Health of the Department of Health and Human Services shall

designate and appoint, for the enforcement of this chapter, a Commissioner and

such other agents as he or she may deem necessary.

      [14:177:1939; 1931 NCL § 6206.13]—(NRS A 1959, 616;

1963, 972; 1967, 1178; 1969, 616)

      NRS 585.210  Regulations.

      1.  The authority to promulgate regulations

for the efficient enforcement of this chapter is hereby vested in the Commissioner.

      2.  The Commissioner is hereby authorized

to make the regulations promulgated under this chapter conform, insofar as

practicable, with those promulgated under the Federal Act.

      [Part 15:177:1939; 1931 NCL § 6206.14]

      NRS 585.220  Hearings.  Hearings

authorized or required by this chapter shall be conducted by the Commissioner

or such officer, agent or employee as the Commissioner may designate for the

purpose.

      [Part 15:177:1939; 1931 NCL § 6206.14]

      NRS 585.230  Record of adulterated, mislabeled or misbranded foods, drugs,

devices and cosmetics; biennial report of Commissioner; dissemination of

information.

      1.  The Commissioner shall keep a record of

adulterated, mislabeled or misbranded foods, drugs, devices and cosmetics, in

which record shall be included a list of cases examined and violations found

and a list of the articles found adulterated, mislabeled or misbranded and the

names of the manufacturers, producers, jobbers and sellers.

      2.  The record, or any parts thereof, may,

in the discretion of the Commissioner, be included in the biennial report which

the Commissioner is authorized to make to the State Board of Health.

      3.  The Commissioner may also cause to be

disseminated such information regarding foods, drugs, devices and cosmetics as

the Commissioner deems necessary in the interest of public health and the

protection of the consumer against fraud.

      [17:177:1939; 1931 NCL § 6206.16]—(NRS A 1959, 617)

      NRS 585.240  Inspection of factories and vehicles: Purposes; examination of

samples.

      1.  The Commissioner or the Commissioner’s

duly authorized agent is entitled to free access at all reasonable hours to any

factory, warehouse or establishment in which foods are manufactured, processed,

packed or held for introduction into commerce, or may enter any vehicle being

used to transport or hold such foods in commerce, for the purpose of:

      (a) Inspecting such factory, warehouse,

establishment or vehicle to determine whether any of the provisions of this

chapter is being violated; and

      (b) Securing samples or specimens of any food

after paying or offering to pay for such sample.

      2.  The Commissioner shall make, or cause

to be made, examinations of samples secured under the provisions of this

section to determine whether any provision of this chapter is being violated.

      [16:177:1939; 1931 NCL § 6206.15]—(NRS A 1979, 1192)

      NRS 585.245  Licensing of persons manufacturing, compounding, processing or

packaging drugs, devices or cosmetics: Regulations; fees; inspection.

      1.  The Commissioner shall adopt

regulations for the licensing of every person who manufactures, compounds,

processes or packages drugs, devices or cosmetics in a factory, warehouse,

laboratory or other location in this State. The regulations must set forth the

requirements for issuance and renewal of a license. Only a person who complies

with the requirements of this chapter is entitled to a license. A license is

not transferable from person to person or from place to place. The regulations

must prescribe the length of term for which a license is issued and must set

forth grounds and procedures for the revocation, suspension or nonrenewal of a

license.

      2.  A valid license is required for the

manufacturing, compounding, processing or packaging of drugs, devices or

cosmetics in any factory, warehouse, laboratory or other location in this

State. Licensed pharmacies compounding or packaging prescriptions are exempt

from this provision.

      3.  The Commissioner shall establish and

collect fees for the purpose of paying the costs of inspecting, testing and

other functions required under the provisions of this chapter with respect to

any drug, device or cosmetic. Failure to pay any fee imposed pursuant to this

subsection is a ground for revocation, suspension or nonrenewal of a license.

All such fees collected by the Commissioner must be deposited with the State

Treasurer for credit to the State General Fund.

      4.  As a condition for entertaining the

application of any applicant for any license authorized under this chapter, and

as a further condition for the issuance of any such license, the Commissioner

or the Commissioner’s authorized agent is entitled to free access at all

reasonable hours to any factory, warehouse or other location in which drugs,

devices or cosmetics are manufactured, compounded, processed or packaged or

held for introduction into commerce, and may enter any vehicle being used to

transport or hold such drugs, devices or cosmetics in commerce, for the

purposes of:

      (a) Inspecting the factory, warehouse, other

location or vehicle to determine whether any of the provisions of this chapter

is being violated; and

      (b) Securing samples or specimens of any drug,

device or cosmetic after paying or offering to pay therefor.

      5.  The Commissioner shall make, or cause

to be made, examinations of samples and specimens secured under the provisions

of this section to determine whether any of the provisions of this chapter is

being violated.

      (Added to NRS by 1979, 1191)

      NRS 585.250  Tagging of articles believed to be dangerous to health: Contents

of tag; unlawful sales.

      1.  Whenever the Commissioner, any of the

Commissioner’s authorized agents, or any member or inspector of the State Board

of Pharmacy finds, or has probable cause to believe, that any food, drug,

device or cosmetic is adulterated, or so misbranded as to be dangerous or

fraudulent, within the meaning of this chapter, he or she shall affix to such

article a tag or other appropriate marking, giving notice that such article is,

or is suspected of being, adulterated or misbranded and has been quarantined,

and warning all persons not to remove or dispose of such article by sale or

otherwise until permission for removal or disposal is given by such agent or

the court.

      2.  It shall be unlawful for any person to

remove or dispose of such quarantined article by sale or otherwise without such

permission.

      [Part 4:177:1939; 1931 NCL § 6206.03]—(NRS A 1967,

1665)

      NRS 585.260  Removal of tag or marking from detained or quarantined article;

liability of person removing tag or other marking.

      1.  When the Commissioner, the

Commissioner’s authorized agent, or a member or inspector of the State Board of

Pharmacy has found that an article so quarantined is not adulterated or

misbranded, he or she shall remove the tag or other marking.

      2.  In any proceeding against the

Commissioner, the Commissioner’s authorized agent, or a member or inspector of

the State Board of Pharmacy because of such quarantine, the Commissioner, the

Commissioner’s authorized agent, or member or inspector of the State Board of

Pharmacy shall not be held liable if the court shall find that there was

probable cause for such quarantine.

      [Part 4:177:1939; 1931 NCL § 6206.03]—(NRS A 1967,

1666)

      NRS 585.270  Petition for condemnation and destruction of adulterated or

misbranded article.  When an

article quarantined under NRS 585.250 has been

found by the Commissioner, the Commissioner’s authorized agent, or a member or

inspector of the State Board of Pharmacy to be adulterated or misbranded, the

Commissioner, the Commissioner’s agent, or such member or inspector shall

petition the judge of the district court in whose jurisdiction the article is

quarantined for the condemnation and destruction of such article.

      [Part 4:177:1939; 1931 NCL § 6206.03]—(NRS A 1967,

1666)

      NRS 585.280  Destruction of article found to be adulterated or misbranded.  If the court finds that a quarantined article

is adulterated or misbranded, such article shall, after entry of the decree, be

destroyed under the supervision of the Commissioner, the Commissioner’s

authorized agent, or a member or inspector of the State Board of Pharmacy.

      [Part 4:177:1939; 1931 NCL § 6206.03]—(NRS A 1967,

1666)

      NRS 585.290  Correction of defect by proper labeling or processing.  When the adulteration or misbranding can be

corrected by proper labeling or processing of the article to the satisfaction

of the Commissioner, the Commissioner’s authorized agent, or a member or

inspector of the State Board of Pharmacy, the court, after entry of the decree,

may by order direct that such article be delivered to the owner or defender

thereof for such labeling or processing under the supervision of the

Commissioner, the Commissioner’s authorized agent, or a member or inspector of

the State Board of Pharmacy.

      [Part 4:177:1939; 1931 NCL § 6206.03]—(NRS A 1967,

1666)

FOOD

      NRS 585.300  Adulterated food: Poisonous or insanitary ingredients.  A food shall be deemed to be adulterated if:

      1.  It bears or contains any poisonous or

deleterious substance which may render it injurious to health unless the

substance is not an added substance and the quantity of the substance does not

ordinarily render it injurious to health;

      2.  It consists in whole or in part of a

diseased, contaminated, filthy or decomposed substance, or if it is otherwise

unfit for food;

      3.  It has been produced, prepared, packed

or held under insanitary conditions whereby it may have become contaminated

with filth or rendered diseased, unwholesome or injurious to health;

      4.  It is the product of an animal which

was diseased, died otherwise than by slaughter or was fed upon the uncooked

offal from a slaughterhouse;

      5.  Its container is composed, in whole or

in part, of any poisonous or deleterious substance which may render the

contents injurious to health; or

      6.  It bears or contains any color additive

which is unsafe within the meaning of the Federal Act.

      [Part 6:177:1939; 1931 NCL § 6206.05]—(NRS A 1983, 190)

      NRS 585.310  Adulterated food: Absence, substitution or addition of

constituents.  A food shall be

deemed to be adulterated:

      1.  If any valuable constituent has been in

whole or in part omitted or abstracted therefrom;

      2.  If any substance has been substituted

wholly or in part therefor;

      3.  If damage or inferiority has been

concealed in any manner; or

      4.  If any substance has been added thereto

or mixed or packed therewith so as to increase its bulk or weight, or reduce

its quality or strength, or make it appear better or of greater value than it

is.

      [Part 6:177:1939; 1931 NCL § 6206.05]

      NRS 585.320  Adulterated food: Standards of purity, quality or strength.  A food shall be deemed to be adulterated if it

falls below the standard of purity, quality or strength which it purports or is

represented to possess.

      [Part 6:177:1939; 1931 NCL § 6206.05]

      NRS 585.330  Adulterated food: Confectionery containing nonnutritive

substance.

      1.  A food shall be deemed to be

adulterated if it is confectionery and it bears or contains any nonnutritive

article or substance except harmless coloring, harmless flavoring, harmless

resinous glaze not in excess of four-tenths of 1 percent, harmless natural wax

not in excess of four-tenths of 1 percent, harmless natural gum and pectin.

      2.  This section does not apply to any

confectionery by reason of its containing less than 4 percent alcohol by

weight, or to any chewing gum by reason of its containing harmless nonnutritive

masticatory substances.

      [Part 6:177:1939; 1931 NCL § 6206.05]—(NRS A 1981, 908)

      NRS 585.350  Misbranded food.  A

food shall be deemed to be misbranded:

      1.  If its labeling is false or misleading

in any particular.

      2.  If it is offered for sale under the

name of another food.

      3.  If it is an imitation of another food,

unless its label bears, in type of uniform size and prominence, the word

“Imitation,” and immediately thereafter the name of the food imitated.

      4.  If its container is so made, formed or

filled as to be misleading.

      5.  If it is not labeled as required by NRS 583.045.

      6.  If in package form, unless it bears a

label containing:

      (a) The name and place of business of the

manufacturer, packer or distributor.

      (b) An accurate statement of the quantity of the

contents in terms of weight, measure or numerical count; but under this

paragraph reasonable variations shall be permitted, and exemptions as to small

packages shall be established by regulation prescribed by the Commissioner.

      7.  If it purports to be or is represented

as a food for which a definition and standard of identity, quality and fill of

container has been prescribed, unless it conforms to such standards of

identity, quality and fill.

      8.  If it purports to be or is represented

for special dietary uses, unless its label bears such information concerning

its vitamin, mineral and other dietary properties as the Commissioner

determines to be, and by regulations prescribes as, necessary in order to

inform purchasers fully as to its value for such uses.

      9.  If it bears or contains any artificial

flavoring, artificial coloring, or chemical preservative, unless it bears

labeling stating that fact; but the provisions of this subsection with respect

to artificial color shall not apply in the case of butter, cheese or ice cream.

      [7:177:1939; 1931 NCL § 6206.06]—(NRS A 1965, 433)

      NRS 585.355  Use of “honey” in product label or designation restricted;

“honey” defined.  A person shall

not prepare, package, deliver for shipment, ship, transport or sell:

      1.  Any food product which is labeled or

designated by the term “honey” alone if such food product consists partly or

entirely of ingredients other than honey.

      2.  Any food product, except a honeydew

melon, designated by any combination of words which include the word “honey” in

the label or brand name unless such food product contains honey as an

ingredient and the other ingredients are disclosed.

Ê As used in

this section, “honey” means the natural product of honeybees, drawn from the

nectar of flowers, transformed by the bees and stored in a honeycomb and later

marketed in the honeycomb or taken from it and marketed in a liquid, candied or

granulated condition.

      (Added to NRS by 1975, 813)

      NRS 585.360  Food containing filthy, decomposed or putrid substance declared

nuisance; condemnation or destruction by Commissioner.  Whenever

the Commissioner or any of the Commissioner’s authorized agents shall find in

any room, building or other structure, or vehicle of transportation, any meat,

seafood, poultry, vegetable, fruit or other perishable articles which are

unsound, or contain any filthy, decomposed or putrid substance, or that may be

poisonous or deleterious to health or otherwise unsafe, the same being hereby

declared to be a nuisance, the Commissioner or the Commissioner’s authorized

agents shall forthwith condemn or destroy the same, or in any other manner render

the same unsalable as human food.

      [Part 4:177:1939; 1931 NCL § 6206.03]

DRUGS AND DEVICES

      NRS 585.370  Adulterated drugs and devices: Poisonous or insanitary

ingredients.  A drug or device

shall be deemed to be adulterated if:

      1.  It consists in whole or in part of any

filthy or decomposed substance;

      2.  It has been produced, prepared, packed

or held under insanitary conditions whereby it may have been rendered injurious

to health;

      3.  It is a drug and its container is

composed, in whole or in part, of any poisonous or deleterious substance which

may render the contents injurious to health; or

      4.  It is a drug and it bears or contains,

for coloring only, a color additive which is unsafe within the meaning of the

Federal Act.

      [Part 8:177:1939; 1931 NCL § 6206.07]—(NRS A 1983, 190)

      NRS 585.380  Adulterated drugs and devices: Strength, quality or purity

differing from official compendium.

      1.  A drug shall be deemed to be

adulterated if it is represented as a drug, the name of which is recognized in

an official compendium, and its strength differs from, or its quality or purity

falls below, the standard set forth in the compendium. The determination as to

strength, quality or purity must be made in accordance with the tests or

methods of assay set forth in the compendium or, in the absence of or

inadequacy of those tests or methods of assay, those prescribed pursuant to the

Federal Act.

      2.  A drug which is defined in an official

compendium shall not be deemed to be adulterated under this section because it

differs from the standard of strength, quality or purity set forth in the

compendium if that difference is plainly stated on its label.

      [Part 8:177:1939; 1931 NCL § 6206.07]—(NRS A 1983, 190)

      NRS 585.390  Adulterated drugs and devices: Misrepresentation of strength,

quality or purity if drug not in compendium.  A

drug or device shall be deemed to be adulterated if it is not subject to the

provisions of NRS 585.380 and its strength differs

from, or its purity or quality falls below, that which it purports or is

represented to possess.

      [Part 8:177:1939; 1931 NCL § 6206.07]

      NRS 585.400  Adulterated drugs and devices: Mixture with or substitution of

another substance.  A drug or

device shall be deemed to be adulterated if it is a drug and any substance has

been:

      1.  Mixed or packed therewith so as to

reduce its quality or strength; or

      2.  Substituted wholly or in part therefor.

      [Part 8:177:1939; 1931 NCL § 6206.07]

      NRS 585.410  Misbranded drugs and devices: False or misleading label.  A drug or device shall be deemed to be

misbranded if its labeling is false or misleading in any particular.

      [Part 9:177:1939; 1931 NCL § 6206.08]

      NRS 585.420  Misbranded drugs and devices: Contents of label on package.

      1.  Except as provided in subsections 2 and

3, a drug or device shall be deemed to be misbranded if in package form unless

it bears a label containing:

      (a) The name and place of business of the

manufacturer, packer or distributor; and

      (b) An accurate statement of the quantity of the

contents in terms of weight, measure or numerical count.

      2.  The label affixed to a container which

contains a prescription drug intended for use by a human being shall include:

      (a) The name and place of business of the

manufacturer; and

      (b) If different, the name and place of business

of the packer or distributor,

Ê of the drug

in its final dosage form.

      3.  A label affixed to a container by a

pharmacist is not required to include the name and place of business of the

manufacturer, packer or distributor.

      4.  Under paragraph (b) of subsection 1,

reasonable variations shall be permitted, and exemptions as to small packages

shall be established, by regulations prescribed by the Commissioner.

      [Part 9:177:1939; 1931 NCL § 6206.08]—(NRS A 1977, 632)

      NRS 585.430  Misbranded drugs and devices: Habit-forming substances.  A drug or device shall be deemed to be

misbranded if it is for use by humans and contains any quantity of narcotic or

hypnotic substances or any chemical derivative thereof, unless its label bears

the name and quantity or proportion of such substance or derivative and, in

juxtaposition therewith, the statement “Warning—May be habit forming.”

      [Part 9:177:1939; 1931 NCL § 6206.08]

      NRS 585.440  Misbranded drugs and devices: Designation of drug by name not in

compendium.

      1.  A drug or device shall be deemed to be

misbranded if it is a drug and is not designated solely by a name recognized in

an official compendium unless its label bears:

      (a) The common or usual name of the drug, if such

there be; and

      (b) In case it is fabricated from two or more

ingredients, the common or usual name of each active ingredient, including the

kind and quantity or proportion of any alcohol, and also including, whether

active or not, the name and quantity or proportion of any bromide, ether,

chloroform, acetanilid, acetophenetidin, amidopyrine, antipyrine, atropine,

hyoscine, hyoscyamine, arsenic, digitalis, digitalis glucosides, mercury,

ouabain, strophanthin, strychnine, thyroid, or any derivative or preparation of

any such substances contained therein.

      2.  To the extent that compliance with the

requirements of paragraph (b) of subsection 1 is impracticable, exemptions

shall be established by regulations promulgated by the Commissioner.

      [Part 9:177:1939; 1931 NCL § 6206.08]

      NRS 585.450  Misbranded drugs and devices: Directions for use and warnings on

label.

      1.  A drug or device shall be deemed to be

misbranded unless its label bears:

      (a) Adequate directions for use; and

      (b) Such adequate warnings against use in those

pathological conditions or by children where its use may be dangerous to

health, or against unsafe dosage or methods or duration or administration or

application, in such manner and form as are necessary for the protection of

users.

      2.  Where any requirement of paragraph (a)

of subsection 1, as applied to any drug or device, is not necessary for the

protection of the public health, the Commissioner shall promulgate regulations

exempting such drug or device from such requirements.

      [Part 9:177:1939; 1931 NCL § 6206.08]

      NRS 585.460  Misbranded drugs and devices: Misleading container; imitation;

offer for sale under another name.  A

drug or device shall be deemed to be misbranded:

      1.  If it is a drug and its container is so

made, formed or filled as to be misleading;

      2.  If it is an imitation of another drug;

or

      3.  If it is offered for sale under the

name of another drug.

      [Part 9:177:1939; 1931 NCL § 6206.08]

      NRS 585.470  Misbranded drugs and devices: Health-endangering when used as

prescribed.  A drug or device shall

be deemed to be misbranded if it is dangerous to health when used in the dosage

or with the frequency or duration prescribed, recommended or suggested in the

labeling thereof.

      [Part 9:177:1939; 1931 NCL § 6206.08]

      NRS 585.480  Misbranded drugs and devices: Drug containing amidopyrine,

barbituric acid, cinchophen, dinitrophenol or sulfanilamide sold without

prescription.  A drug or device

shall be deemed to be misbranded if it is a drug sold at retail for use by

humans, and contains any quantity of amidopyrine, barbituric acid, cinchophen,

dinitrophenol or sulfanilamide, unless it is sold on a written prescription

signed by a member of the medical, dental or veterinary profession who is

licensed by law to administer such drug, and its label bears the name and place

of business of the seller, the serial number and date of such prescription, and

the name of such member of the medical, dental or veterinary profession.

      [Part 9:177:1939; 1931 NCL § 6206.08]

      NRS 585.485  Restrictions on sale of dimethyl sulfoxide; penalty.

      1.  Dimethyl sulfoxide may be sold, whether

by wholesalers or retailers, in quantities of 1 gallon or more.

      2.  Dimethyl sulfoxide may be sold,

prescribed or dispensed in quantities of less than 1 gallon only:

      (a) Pursuant to prescription by a dentist,

podiatric physician or veterinarian licensed to practice such profession in

this State or by a licensed physician; or

      (b) To a purchaser who gives an affidavit

declaring that the dimethyl sulfoxide being purchased:

             (1) Will not be used for medicinal

treatment of any human being; or

             (2) Will not be resold and will be used

for industrial or commercial purposes in a laboratory or business which is

licensed by the state or a local government.

      3.  A prescription for dimethyl sulfoxide

may be filled only with a grade and quality of that substance which meets the

requirements of the United States Food and Drug Administration.

      4.  Any person who gives a false affidavit

for the purpose of obtaining dimethyl sulfoxide pursuant to paragraph (b) of

subsection 2 is guilty of a misdemeanor.

      (Added to NRS by 1981, 1696; A 1993, 2237)

      NRS 585.490  Introduction or delivery for introduction of new drug into

intrastate commerce before application is effective prohibited.  No person shall introduce or deliver for

introduction into intrastate commerce any new drug which is subject to section

505 of the Federal Act (21 U.S.C. § 355), unless an application with respect to

such drug has become effective thereunder.

      [10:177:1939; 1931 NCL § 6206.09]

      NRS 585.495  Licensing of manufacture of amygdalin and procaine

hydrochloride; duties and powers of Commissioner; injunctive relief.

      1.  The State Board of Health shall license

amygdalin (laetrile) and procaine hydrochloride with preservatives and

stabilizers (Gerovital H3) for manufacture in this state. Such licensing is not

a representation that either substance has any therapeutic effect.

      2.  The Commissioner shall:

      (a) Adopt regulations which prescribe minimum

standards for manufacturers in preparing, compounding, processing and packaging

each substance.

      (b) Make periodic tests and inspections of both

the facilities for manufacture and samples of the substances to ascertain the

purity, quality and identity of the substance and to determine that the

substance meets the standards prescribed pursuant to paragraph (a).

      (c) Before acting upon an application for a

license, collect the fees necessary to pay the cost of investigating the

applicant. A license shall not be issued until the applicant has paid all

actual costs for the initial testing, inspection, investigation and hearings.

      3.  The Commissioner may, after notice and

hearing, revoke, suspend or refuse to renew the license of any person who:

      (a) Fails to maintain the standards required by

paragraph (b) of subsection 2.

      (b) Violates any regulation adopted by the

Commissioner.

      (c) Fails to pay any assessment prescribed in

paragraph (c) of subsection 2 within a reasonable time.

      4.  The Attorney General shall, at the

request of the Commissioner seek injunctive relief for any violation of the

regulations adopted by the Commissioner.

      (Added to NRS by 1977, 1646; A 1979, 1193; 1983, 224)

      NRS 585.497  Assessment on gross receipts from sale of amygdalin and procaine

hydrochloride.

      1.  An assessment of 10 percent, payable

quarterly to the Department of Taxation, is imposed upon the gross receipts of

a manufacturer from the sale of each substance licensed for manufacture

pursuant to NRS 585.495.

      2.  The Nevada Tax Commission shall

prescribe by regulation appropriate forms for reporting such gross receipts,

and shall when appropriate recompute the assessment and collect any deficiency

in the manner provided for taxes required to be paid pursuant to title 32 of

NRS. Each manufacturer shall report the sales and pay the assessment during the

months of January, April, July and October for the respective preceding

calendar quarters.

      3.  As used in this section:

      (a) “Gross receipts” means the total amount of

the sale of each substance, valued in money, whether received in money or

otherwise, without deduction for any of the following:

             (1) The cost of the substance sold.

             (2) The cost of the materials used, labor

or service, any interest paid or any losses or other expense.

             (3) The cost of marketing the substance.

             (4) The cost of transporting the substance

before its sale to the purchaser.

      (b) “Sale” includes any transfer of title or

possession, exchange or barter, whether conditional or otherwise, of a

substance for a consideration.

      (c) “Total amount of the sale” includes:

             (1) Any services that are a part of the

sale; and

             (2) All receipts, cash, credits and

property of any kind.

      (Added to NRS by 1983, 223)

COSMETICS

      NRS 585.500  Adulterated cosmetics.  A

cosmetic shall be deemed to be 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 or advertisement thereof, or under

such conditions of use as are customary or usual; but this provision shall not

apply to coal tar hair dye, the label of which bears the following legend

conspicuously displayed thereon: “Caution—This product contains ingredients

which may cause irritation on certain individuals and a preliminary test

according to accompanying directions should first be made. This product must

not be used for dyeing the eyelashes or eyebrows; to do so may cause

blindness.”, and the labeling of which bears adequate directions for such

preliminary testing. For the purposes of this subsection and subsection 5 the

term “hair dye” shall not include eyelash or eyebrow dyes.

      2.  If it consists in whole or in part of

any filthy, putrid or decomposed substance.

      3.  If it has been produced, prepared,

packed or held under insanitary conditions whereby it may have become

contaminated with filth, or whereby it may have been 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.

      5.  If it is not a hair dye and it bears or

contains a coal tar color other than one from a batch which has been certified

by the United States Department of Agriculture.

      [11:177:1939; 1931 NCL § 6206.10]

      NRS 585.510  Misbranded cosmetics.  A

cosmetic shall be deemed to be misbranded:

      1.  If its labeling is false or misleading

in any particular.

      2.  If in package form unless it bears a

label containing:

      (a) The name and place of business of the manufacturer,

packer or distributor; and

      (b) An accurate statement of the quantity of the

contents in terms of weight, measure or numerical count. Under this paragraph,

reasonable variations shall be permitted, and exemptions as to small packages

shall be established by regulations prescribed by the Commissioner.

      3.  If its container is so made, formed or

filled as to be misleading.

      [12:177:1939; 1931 NCL § 6206.11]

PROHIBITED ACTS AND PENALTIES

      NRS 585.520  Prohibited acts.  The

following acts and the causing thereof within the State of Nevada are hereby

prohibited:

      1.  The manufacture, sale or delivery,

holding or offering for sale of any food, drug, device or cosmetic that is

adulterated or misbranded.

      2.  The adulteration or misbranding of any

food, drug, device or cosmetic.

      3.  The sale, delivery for sale, holding

for sale or offering for sale of any article in violation of NRS 585.490.

      4.  The dissemination of any false

advertisement.

      5.  The refusal to permit entry or

inspection, or to permit the taking of a sample, as authorized by NRS 585.240 or 585.245.

      6.  The giving of a guaranty or

undertaking, which guaranty or undertaking is false, except by a person who

relied on a guaranty or undertaking to the same effect signed by and containing

the name and address of the person residing in the State of Nevada from whom he

or she received in good faith the food, drug, device or cosmetic.

      7.  The removal or disposal of a detained

or embargoed article in violation of NRS 585.250.

      8.  The alteration, mutilation,

destruction, obliteration or removal of the whole or any part of the labeling

of or the doing of any other act with respect to a food, drug, device or

cosmetic, if such act is done while such article is held for sale and results

in such article being misbranded.

      [3:177:1939; 1931 NCL § 6206.02]—(NRS A 1979, 1193)

      NRS 585.530  When advertisement deemed false.  An

advertisement of a food, drug, device or cosmetic shall be deemed to be false

if it is false or misleading in any particular.

      [13:177:1939; 1931 NCL § 6206.12]

      NRS 585.535  Unlawful to sell or offer to sell beverage container opened by

detaching metal ring or tab; exceptions; penalty.

      1.  Except as otherwise provided in

subsection 2, it is unlawful for a person to sell or offer for sale at retail a

metal beverage container so designed and constructed that it is opened by

detaching a metal ring or tab.

      2.  This section does not prohibit the sale

of a beverage container which:

      (a) Is sealed with laminated tape, foil or other

soft material that is detachable; or

      (b) Contains milk-based, soy-based or similar

products which require heat and pressure in the canning process.

      3.  A person who violates the provisions of

subsection 1 shall be punished by a fine of not more than $500 for each

violation. Each day of violation constitutes a separate offense.

      (Added to NRS by 1989, 277)

      NRS 585.540  Duties of Attorney General and district attorneys; hearing by

Commissioner before institution of criminal proceedings.

      1.  The Attorney General or any district

attorney to whom the Commissioner or any of the Commissioner’s authorized

agents shall report any violation of this chapter shall cause appropriate

proceedings to be instituted in the proper court without delay and to be

prosecuted in the manner required by law.

      2.  Before any violation of this chapter is

reported to the Attorney General or a district attorney for the institution of

a criminal proceeding, the person against whom such proceeding is contemplated

shall be given appropriate notice and an opportunity to present his or her

views before the Commissioner or the Commissioner’s designated agent, either

orally or in writing, in person or by attorney, with regard to such

contemplated proceeding.

      [5:177:1939; 1931 NCL § 6206.04]

      NRS 585.550  Penalties.

      1.  A person who manufactures, compounds,

processes or packages any drug in a factory, warehouse, laboratory or other

location in this state without a license required by NRS

585.245 is guilty of a category D felony and shall be punished as provided

in NRS 193.130.

      2.  A person who violates any other

provision of this chapter is guilty of a gross misdemeanor.

      [18:177:1939; 1931 NCL § 6206.17]—(NRS A 1967, 619; 1979, 1194; 1995, 1306)