New Jersey § 24:1-1

§ 24:1-1.

As used in this Title: a. “ State department ,” “ department of health ” and “ department ” mean the “State Department of Health.” b. “ Council ” means the Public Health Council in the State Department of Health. c. “ Local board ” or “ local board of health ” means the board of health of any municipality, or the boards, bodies, or officers

in such municipality lawfully exercising the powers of a local board of health under

the laws governing such municipality, and includes any consolidated local board of

health or county local board of health created and established pursuant to law. d. “ Food ” means (1) articles used for food or drink for man or other animals (2) chewing gum

and (3) articles used for components of any such article. e. “ Drug ” means (1) 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; and (2) articles intended for use in the diagnosis,

cure, mitigation, treatment or prevention of disease in man or other animals; and

(3) articles (other than food) intended to affect the structure or any function of

the body of man or other animals; and (4) articles intended for use as a component

of any article specified in (1), (2), or (3) of this definition ; but does not include biological products, or devices or their components, parts,

or accessories. The term “drug” also does not include: hemp and hemp products cultivated, handled,

processed, transported, or sold pursuant to the “New Jersey Hemp Farming Act,” P.L.2019, c. 238 ( C.4:28-6 et al.); cannabis as defined in section 3 of P.L.2021, c. 16 ( C.24:6I-33 ) which is cultivated and produced for use in a cannabis item, as defined in that

section, in accordance with the “New Jersey Cannabis Regulatory, Enforcement Assistance,

and Marketplace Modernization Act,” P.L.2021, c. 16 ( C.24:6I-31 et al.); and cannabis resin as defined in that section 3 ( C.24:6I-33 ) which is extracted for use in a cannabis item, as defined in that section, in accordance

with that act. f. “ Package ” or “ container ” means wrapper, case, basket, hamper, can, bottle, jar, tube, cask, vessel, tub,

firkin, keg, jug, barrel, or other receptacles, but the word, “package” shall not

include open containers which permit a visual and physical inspection by the purchaser

at retail, nor bags and other receptacles which are filled in the presence of the

purchaser at retail. g. “ 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 man or other animals; or (2) to affect the structure

or any function of the body of man or other animals. h. “ Cosmetic ” means (1) 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, and (2) articles intended for

use as a component of any such articles; except that such term shall not include

soap. i. “ New drug ” means (1) any drug the composition of which is such that such drug is not generally

recognized, among experts qualified by scientific training and experience to evaluate

the safety of drugs, as safe for use under the conditions prescribed, recommended,

or suggested in the labeling thereof, and (2) any drug the composition of which is

such that such drug, as a result of investigations to determine its safety for use

under such conditions, has become so recognized, but which has not, otherwise than

in such investigations, been used to a material extent or for a material time under

such conditions. j. “ 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 subtitle 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 any there be, of the retail package of such

article, or is easily legible through the outside container or wrapper. The term “immediate container” does not include package liners. k. “ 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. l. “ 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. m. If an article is alleged to be misbranded because the labeling is misleading, then

in determining whether such labeling is misleading there shall be taken into account , among other things , not only representations made or suggested by statement, word, design, or any combination

thereof, but also the extent to which such labeling 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 such labeling relates under the conditions

of use prescribed in the labeling thereof or under such conditions of use as are customary

or usual. n. The representation of a drug 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. o. The provisions of this act regarding the selling of food, drugs, devices, or cosmetics,

shall be considered to include the manufacture, production, processing, packing, exposure,

offer, possession, and holding of any such article for sale; and the sale, dispensing,

and giving away of any such article and the supplying or applying of any such articles

in the conduct of any food, drug or cosmetic establishment. p. The term “ Federal Act ” means the Federal Food, Drug and Cosmetic Act ( Title 21, U.S.C. s.301 et seq. ; 52 Stat. 1040 et seq.).