New Jersey Revised Statutes
Title 24 - Food and Drugs
Section 24:6I-7.1 - Acceptance, processing of applications.

24:6I-7.1 Acceptance, processing of applications.
11. a. The commission shall, no later than 90 days after the effective date of P.L.2019, c.153 (C.24:6I-5.1 et al.) or upon adoption of rules and regulations as provided in subsection c. of section 18 of P.L.2009, c.307 (C.24:6I-16), whichever occurs later, begin accepting and processing applications for new medical cannabis cultivator, medical cannabis manufacturer, and medical cannabis dispensary permits. Notwithstanding the provisions of subsubparagraph (i) of subparagraph (a) of paragraph (2) of subsection a. of section 7 of P.L.2009, c.307 (C.24:6I-7), the first three alternative treatment center permits issued by the commission pursuant to an application submitted on or after the effective date of P.L.2019, c.153 (C.24:6I-5.1 et al.) and up to four alternative treatment centers permits issued by the commission after the effective date of P.L.2019, c.153 (C.24:6I-5.1 et al.) pursuant to an application submitted pursuant to a request for applications published in the New Jersey Register prior to the effective date of P.L.2019, c.153 (C.24:6I-5.1 et al.) shall be deemed to concurrently hold a medical cannabis cultivator permit, a medical cannabis manufacturer permit, and a medical cannabis dispensary permit; of these permits, one permit shall be issued to an applicant located in the northern region of the State, one permit shall be issued to an applicant located in the central region of the State, and one permit shall be issued to an applicant located in the southern region of the State. Any permits issued by the commission thereafter shall be subject to the provisions of subsubparagraph (i) of subparagraph (a) of paragraph (2) of subsection a. of section 7 of P.L.2009, c.307 (C.24:6I-7), and the requirements of subsection d. of this section concerning conditional permits.
b. The commission may establish nonrefundable application fees for permit applications and conditional permit applications, and permit and conditional permit fees for successful applicants.
c. (1) The commission shall make a determination as to any permit application, other than an application for a conditional permit submitted pursuant to subsection d. of this section, no later than 90 days after receiving the application, which may include a determination that the commission reasonably requires more time to adequately review the application.
(2) The commission shall issue a permit, other than a conditional permit, to an approved applicant at such time as the commission completes the application review process and any mandatory inspections, and determines that the applicant is in compliance with and is implementing the plans, procedures, protocols, actions, or other measures set forth in the applicant's permit application submitted pursuant to section 12 of P.L.2019, c.153 (C.24:6I-7.2), did maintain compliance with the terms, conditions, or restrictions of a conditional permit issued to the applicant, if applicable, and is otherwise in compliance with the requirements of P.L.2009, c.307 (C.24:6I-1 et al.).
d. (1) The commission shall ensure that at least one third of the total permits issued for each type of medical cannabis permit are conditional permits, which one-third figure shall include any conditional permit issued to an applicant which is subsequently converted by the commission into a full permit pursuant to paragraph (4) of this subsection and any conditional permit, including a converted permit, issued to a microbusiness pursuant to subsection e. of this section. The requirements of this subsection shall not apply to permits issued to clinical registrants or to permits issued to the three alternative treatment centers issued a permit pursuant to subsection a. of this section that are expressly exempt from the provisions of subsubparagraph (i) of subparagraph (a) of paragraph (2) of subsection a. of section 7 of P.L.2009, c.307 (C.24:6I-7).
(2) An application for a conditional permit shall include:
(a) documentation that the applicant entity includes at least one significantly involved person who has resided in this State for at least two years as of the date of the application;
(b) a list of all owners, officers, directors, and employees of, and significantly involved persons in, the proposed medical cannabis entity, including their names, addresses, dates of birth, resumes, and a photocopy of their driver's licenses or other government-issued form of identification;
(c) a criminal history record background check completed pursuant to subsection d. of section 7 of P.L.2009, c.307 (C.24:6I-7) for each owner, officer, director, and employee of, and each significantly involved person in, the proposed medical cannabis entity, provided that a conditional permit may be issued pending the results of a criminal history record background check;
(d) documentation that each significantly involved person in the proposed medical cannabis entity has, for the immediately preceding taxable year, an adjusted gross income of no more than $200,000 or no more than $400,000 if filing jointly with another;
(e) a certification that each significantly involved person in the proposed medical cannabis entity does not have any financial interest in an entity applying for any other medical cannabis permit, or in an entity that currently holds a permit issued pursuant to section 7 of P.L.2009, c.307 (C.24:6I-7);
(f) the federal and State tax identification numbers for the proposed medical cannabis entity, and proof of business registration with the Division of Revenue in the Department of the Treasury;
(g) information about the proposed medical cannabis entity, including its legal name, any registered alternate name under which it may conduct business, and a copy of its articles of organization and bylaws;
(h) the business plan and management operation profile for the proposed medical cannabis entity;
(i) the plan by which the applicant intends to obtain appropriate liability insurance coverage for the proposed medical cannabis entity; and
(j) any other requirements established by the commission pursuant to regulation.
(3) The commission shall make a determination on an application for a conditional permit within 30 days after the date the application is received. A determination made pursuant to this paragraph may include a determination that the commission requires more time to adequately review the application. The commission shall approve a permit application that meets the requirements of this subsection unless the commission finds by clear and convincing evidence that the applicant would be manifestly unsuitable to perform the activities authorized for the permit sought by the applicant. The commission shall deny a conditional permit to any applicant who fails to provide information, documentation, and assurances as required by this subsection; who fails to reveal any fact material to qualification; or who supplies information that is untrue or misleading as to a material fact pertaining to the qualification criteria for issuance of a conditional permit. If the application is denied, the commission shall notify the applicant in writing of the specific reason for its denial and provide the applicant with the opportunity for a hearing in accordance with the "Administrative Procedure Act," P.L.1968, c.410 (C.52:14B-1 et seq.).
(4) The commission shall furnish to each entity issued a conditional permit a list of the requirements that the entity will be required to comply with within 120 days after issuance of the conditional permit. If the commission subsequently determines that, during the 120-day period, the conditional permit holder is in compliance with all applicable conditions and is implementing the plans, procedures, protocols, actions, or other measures set forth in its application, the commission shall convert the conditional permit into a full permit, which will expire one year from its date of issuance and be subject to annual renewal; if the commission determines that the conditional permit holder is not in compliance with all applicable conditions or not implementing the plans, procedures, protocols, actions, or other measures set forth in its application, the conditional permit shall automatically expire at the end of the 120-day period, or, at the discretion of the commission, may be revoked prior to the end of the 120-day period.
(5) A conditional permit issued pursuant this subsection may not be sold or transferred.
e. (1) The commission shall ensure that at least 10 percent of the total permits issued for each medical cannabis permit type, other than a clinical registrant permit, are designated for and only issued to microbusinesses, and that at least 25 percent of the total permits issued be issued to microbusinesses. A microbusiness may be issued a full annual permit pursuant to section 7 of P.L.2009, c.307 (C.24:6I-7) or a conditional permit pursuant to subsection d. of this section. The maximum fee assessed by the commission for issuance or renewal of a permit issued to a microbusiness shall be no more than half the fee applicable to a permit of the same type issued to a person or entity that is not a microbusiness. A permit issued to a microbusiness shall be valid for one year and may be renewed annually.
(2) A microbusiness shall meet the following requirements:
(a) 100 percent of the ownership interest in the microbusiness shall be held by current New Jersey residents who have resided in the State for at least the past two consecutive years;
(b) at least 51 percent of the owners, directors, officers, and employees of the microbusiness shall be residents of the municipality in which the microbusiness is or will be located, or a municipality bordering the municipality in which the microbusiness is or will be located;
(c) the microbusiness shall employ no more than 10 employees at one time, inclusive of any owners, officers, and directors of the microbusiness;
(d) the microbusiness shall not exceed the following size and capacity restrictions:
(i) the entire microbusiness facility shall occupy an area of no more than 2,500 square feet;
(ii) in the case of a microbusiness that is a medical cannabis cultivator, the total medical cannabis grow area shall not exceed 2,500 square feet, measured on a horizontal plane, shall grow no higher than 24 feet above that plane, and shall possess a total of no more than 1,000 plants, including mature and immature medical cannabis plants, but not including seedlings;
(iii) in the case of a microbusiness that is a medical cannabis manufacturer, the manufacturer shall acquire and process no more than 1,000 pounds of medical cannabis in dried form each month; and
(iv) in the case of a microbusiness that is a medical cannabis dispensary, the dispensary shall acquire no more than 1,000 pounds of medical cannabis in dried form, or the equivalent amount in any other form, or any combination thereof, for dispensing to or on behalf of registered qualifying patients each month; and
(e) the microbusiness shall comply with such other requirements as may be established by the commission by regulation.
(3) The requirements of this subsection shall not apply to permits issued pursuant to an application submitted pursuant to a request for applications published in the New Jersey Register prior to the effective date of P.L.2019, c.153 (C.24:6I-5.1 et al.).
f. The commission shall have the authority to review any services agreement submitted pursuant to subsection l. of section 12 of P.L.2019, c.153 (C.24:6I-7.2), and any agreement established under subsubparagraph (ii) of subparagraph (d) of paragraph (2) of subsection a. of section 7 of P.L.2009, c.307 (C.24:6I-7) to provide significant financial or technical assistance or the significant use of intellectual property to an applicant, to determine whether the terms of the agreement, including interest rates, returns, and fees, are commercially reasonable and consistent with the fair market value for the terms generally applicable to agreements of a comparable nature. In the event the commission determines the terms of an agreement are not commercially reasonable or consistent with the fair market value generally applicable to the services to be provided under the agreement, the commission shall have the authority to withhold approval of the permit application until the parties renegotiate a new agreement that, as determined by the commission, is commercially reasonable and consistent with the fair market value for the terms generally applicable to agreements of a comparable nature. The parties to the agreement may request that the commission provide guidance as to what terms it would find to be commercially reasonable and consistent with the fair market value generally applicable to agreements of a comparable nature. Nothing in this subsection shall be construed to require the commission to award a permit to an applicant if the commission determines the applicant does not otherwise meet the requirements for issuance of the permit.
L.2019, c.153, s.11; amended 2021, c.252, s.2.

Structure New Jersey Revised Statutes

New Jersey Revised Statutes

Title 24 - Food and Drugs

Section 24:1-1 - Definitions.

Section 24:1-1.1 - Honey, raw, unprocessed.

Section 24:1-2 - Certain books as evidence

Section 24:1-3 - Responsibility for acts of officers and agents

Section 24:1-4 - Foods, drugs, etc., complying with Federal regulations

Section 24:2-1 - Enforcement by state departments; rules and regulations

Section 24:2-2 - Enforcement by local board

Section 24:2-3 - Appointment of analysts, chemists, specialists, chief inspectors, etc.

Section 24:2-4 - Designation of registered environmental health specialists to perform certain duties.

Section 24:2-5 - Powers, duties of registered environmental health specialist.

Section 24:2-6 - Interference with officials; penalties

Section 24:2-7 - Consolidated certificate of operation; multiple regulated businesses owned operated upon same premises; suspension or revocation

Section 24:2-8 - Fee

Section 24:2-9 - Fees for issuance of "Certificate of Free Sale."

Section 24:3-1 - Right of entry; opening packages; inspection

Section 24:3-2 - Procuring sample of food or drug

Section 24:3-3 - Taking sample without consent of owner

Section 24:3-4 - Preservation of sample

Section 24:3-5 - Proof of analysis as evidence

Section 24:3-6 - Proof of analysis on purchase by other than representative of department

Section 24:3-9 - Composite sample of milk seized in transit

Section 24:4-1 - Confiscation; summary proceeding

Section 24:4-2 - Jurisdiction

Section 24:4-5 - Issuance of warrant

Section 24:4-8 - Claims under oath

Section 24:4-9 - Sale or destruction of condemned article

Section 24:4-10 - Return of goods; bond

Section 24:4-11 - Summary destruction of perishable food

Section 24:4-12 - Adulterated or misbranded foods, drugs, etc.; marking; detaining

Section 24:4A-1 - Short title

Section 24:4A-2 - Definitions.

Section 24:4A-3 - Nonliability for food donated.

Section 24:4A-3.1 - Immunity from liability.

Section 24:4A-4 - Food banks; licenses; fee; regulation

Section 24:4A-4.1 - Online portal to facilitate surplus food donations.

Section 24:4A-5 - Rules and regulations

Section 24:4A-6 - "Healthy Small Food Retailer Act"

Section 24:4A-7 - Findings and declarations relative to small food retailers

Section 24:4A-8 - Definitions relative to small food retailers

Section 24:4A-9, - Implementation of "Healthy Corner Store Program"

Section 24:4A-10 - "Healthy Small Food Retailer Fund" established

Section 24:4A-11 - Grantee report

Section 24:4A-12 - "Jersey Fresh" website expansion

Section 24:4A-13 - Rules, regulations

Section 24:5-1 - Sale, distribution or manufacture of adulterated or misbranded articles

Section 24:5-2 - Certain dealers excepted from operation of pure food and drug law; guaranty of seller

Section 24:5-3 - Content of guaranty; liability of resident seller

Section 24:5-4 - Guaranty by nonresident

Section 24:5-5 - Extent of protection of dealer

Section 24:5-6 - Article for foreign market

Section 24:5-7 - Sale of patent medicines not authorized

Section 24:5-8 - General food adulterations

Section 24:5-9 - Confectionery adulterations

Section 24:5-9.1 - Confectionery with more than 1/2 of 1% alcohol rendered unfit for beverage purposes; sale to person under legal age; label; sign in place of sale; violations; penalty

Section 24:5-10 - General drug or device adulterations

Section 24:5-11 - Exceptions to drug adulterations

Section 24:5-11.1 - General cosmetic adulterations

Section 24:5-13 - Use of wood or methyl alcohol prohibited; penalty

Section 24:5-14 - Meat and meat products

Section 24:5-16 - "Misbranded" defined

Section 24:5-17 - Food misbrandings

Section 24:5-18 - Drug or device misbrandings.

Section 24:5-18.1 - Cosmetic misbrandings

Section 24:5-18.2 - Exemptions from labeling and packaging requirements

Section 24:5-19 - Drugs dispensed by physicians, etc., or on written prescription

Section 24:5-22 - Defacement or removal of label

Section 24:5-23 - Permit to process, manufacture product with hemp, transportation.

Section 24:5A-1 - Short title

Section 24:5A-2 - Definitions

Section 24:5A-3 - Hazardous substance; limitation

Section 24:5A-4 - Application of Federal Hazardous Substances Labeling Act

Section 24:5A-5 - Commissioner; powers

Section 24:5A-6 - Prohibited acts

Section 24:5A-7 - Exceptions

Section 24:5A-8 - Enforcement of act; penalties

Section 24:5A-9 - Action to restrain violations

Section 24:6-1 - Establishment of standards

Section 24:6-2 - Publication: time of taking effect

Section 24:6-3 - Sale or manufacture of nonstandard articles prohibited

Section 24:6A-1 - New drugs; introduction into interstate commerce; application; effective date of application; refusal of application; application of chapter

Section 24:6B-1 - Registration statement, issuance of registration.

Section 24:6B-2 - Registration statement, signature, verification; form and contents.

Section 24:6B-3 - Time for filing

Section 24:6B-4 - Fee

Section 24:6B-5 - Change of address; notice; fee

Section 24:6B-6 - Cleanliness of premises

Section 24:6B-7 - Cleanliness of equipment and machinery

Section 24:6B-8 - Washroom and toilet facilities

Section 24:6B-9 - Adulteration or misbranding of drug; examination of records

Section 24:6B-10 - Order to correct violation

Section 24:6B-11 - Penalties.

Section 24:6B-12 - Definitions.

Section 24:6B-13 - Appropriation

Section 24:6B-14 - Definitions relative to pharmaceutical wholesale distributors.

Section 24:6B-15 - Licensure required for pharmaceutical wholesale distributors.

Section 24:6B-16 - Criminal history record background check for applicants, designated representatives, persons enumerated.

Section 24:6B-17 - Establishment, maintenance of list of authorized distributors.

Section 24:6B-18 - Determination of eligibility for licensure renewal.

Section 24:6B-19 - Additional requirements for designated representatives.

Section 24:6B-20 - Requirements for facilities used for wholesale prescription drug distribution.

Section 24:6B-21 - Provision of pedigree, certification prior to sale, return of prescription drug.

Section 24:6B-22 - Annual report to the Legislature on tracking system.

Section 24:6B-23 - Authentication of distribution of prescription drug.

Section 24:6B-24 - Examination of shipping container.

Section 24:6B-25 - Criteria for return of prescription drug to wholesale distributor.

Section 24:6B-26 - Requirements for wholesale distributor.

Section 24:6B-27 - Maintenance of document, record relative to pedigree, certification.

Section 24:6B-28 - Adherence to written policies, procedures by wholesale distributors.

Section 24:6B-29 - Violations, gradation of offenses.

Section 24:6B-30 - Noncompliance with orders, penalties.

Section 24:6B-31 - Real, personal property, certain, subject to forfeiture.

Section 24:6B-32 - Wholesale Drug Distribution Advisory Council.

Section 24:6B-33 - Rules, regulations.

Section 24:6D-1 - Definitions

Section 24:6D-2 - Offenses

Section 24:6D-3 - Enforcement

Section 24:6E-1 - Short title

Section 24:6E-2 - Advertisement of prescription drugs; rules and regulations

Section 24:6E-3 - Restraint on prescription drug price information to public

Section 24:6E-4 - Definitions.

Section 24:6E-6 - List of interchangeable drug products.

Section 24:6E-7 - Prescriptions; dispensation of lowest cost interchangeable drug product; exceptions; notice of substitution

Section 24:6E-8 - Prescriptions; dispensation of substitute drug for drug not on latest list of interchangeable drug products; reasons; approval of prescriber

Section 24:6E-9 - Dispensation of nonbrand name drug product; label.

Section 24:6E-10 - Signs, information to be disclosed relative to drugs, biological products to be dispensed.

Section 24:6E-11 - Violations; penalties; collection and enforcement; validity of prescription on unauthorized form

Section 24:6E-12 - Inapplicability of act to dispensation of drug permits under institutional permits

Section 24:6E-13 - Severability

Section 24:6F-1 - Prescribing, administering or dispensing amygdalin (laetrile); immunity of physician; written informed request; form

Section 24:6F-2 - Pharmacist; dispensing; immunity from penalty or disciplinary action; affixation of label to container

Section 24:6F-3 - Health care facility or its employee; restriction of use; prohibition; administration or dispensing on prescription; immunity from disciplinary action or penalty

Section 24:6F-4 - Manufacture, introduction or delivery; immunity from liability for civil or criminal penalty

Section 24:6F-5 - Records on use; periodic studies

Section 24:6G-1 - Control or possession without written permit; prohibition; exceptions

Section 24:6G-2 - Sale of nitrous oxide for nonmedical use

Section 24:6G-3 - Record of sale; duration of retention; contents; inspection

Section 24:6G-4 - Permits; purposes authorized

Section 24:6G-5 - Administration and enforcement; rules

Section 24:6G-6 - Violations; penalties; recovery and enforcement

Section 24:6H-1 - Distribution of ephedrine alkaloids to minor, disorderly person; exceptions.

Section 24:6H-2 - Label required on ephedrine alkaloid products.

Section 24:6H-3 - Rules, regulations.

Section 24:6I-1 - Short title.

Section 24:6I-2 - Findings, declarations relative to the medical use of cannabis.

Section 24:6I-3 - Definitions relative to the medical use of cannabis.

Section 24:6I-4 - Registry of qualifying patients, designated, institutional caregivers.

Section 24:6I-5.1 - Authorization process for dispensation.

Section 24:6I-5.2 - Health care practitioner, regulations affecting.

Section 24:6I-5.3 - Qualifying patient from another state, jurisdiction.

Section 24:6I-6 - Applicability of N.J.S.2C:35-18.

Section 24:6I-6.1 - Adverse employment action unlawful.

Section 24:6I-7 - Applications for permits.

Section 24:6I-7.1 - Acceptance, processing of applications.

Section 24:6I-7.2 - Submission of applications to commission.

Section 24:6I-7.3 - Clinical registrant permits.

Section 24:6I-7.4 - Feasibility study for establishing a cannabis research and development permit type.

Section 24:6I-7.5 - Medical advisory board.

Section 24:6I-7.6 - Ineligibility for certain economic incentives.

Section 24:6I-8 - Inapplicability.

Section 24:6I-9 - Falsification of registration card, degree of crime.

Section 24:6I-10 - Written instructions to registered qualifying patient, designated, institutional caregiver.

Section 24:6I-11 - Grants, contributions, use of fees.

Section 24:6I-12 - Reports to Governor, Legislature.

Section 24:6I-13 - Exchange of data, information.

Section 24:6I-14 - Construction of act.

Section 24:6I-15 - Additional immunity.

Section 24:6I-16 - Rules, regulations.

Section 24:6I-17 - Testing of cannabis.

Section 24:6I-18 - Licensing of testing laboratories.

Section 24:6I-19 - Standardized requirements, procedures for testing.

Section 24:6I-20 - Medical cannabis handler certification.

Section 24:6I-21 - Municipalities may authorize consumption areas.

Section 24:6I-22 - System for tracking, cultivating, manufacturing, transfer, dispensing, delivery.

Section 24:6I-23 - Requirements waived by commission.

Section 24:6I-24 - Cannabis Regulatory Commission.

Section 24:6I-25 - Office of Minority, Disabled Veterans, and Women Cannabis Business Development.

Section 24:6I-26 - Criteria for eligibility as employee.

Section 24:6I-27 - Applicability of C.52:13D-12 et seq.; Code of Ethics.

Section 24:6I-28 - Restrictions for commission members, employees.

Section 24:6I-29 - Certain persons prohibited from association with medical cannabis.

Section 24:6I-30 - Severability.

Section 24:6I-31 - Short title.

Section 24:6I-32 - Findings, declarations relative to the regulation and use of cannabis.

Section 24:6I-33 - Definitions relative to the regulation and use of cannabis.

Section 24:6I-34 - Commission activities associated with the personal use of cannabis.

Section 24:6I-35 - Regulation of cannabis.

Section 24:6I-36 - Application for license of conditional license.

Section 24:6I-37 - Class I Cannabis Cultivator license.

Section 24:6I-38 - Grow canopies for licensed cannabis cultivators.

Section 24:6I-39 - Class 2 cannabis manufacturer license.

Section 24:6I-40 - Class 3 cannabis wholesaler license.

Section 24:6I-41 - Class 4 cannabis distributor license.

Section 24:6I-42 - Class 5 cannabis retailer license.

Section 24:6I-43 - Class 6 cannabis delivery license.

Section 24:6I-44 - Personal use cannabis handlers, transportation and delivery of cannabis and cannabis items.

Section 24:6I-45 - Municipal regulations or ordinances.

Section 24:6I-46 - Marketplace regulation.

Section 24:6I-47 - Medical cannabis provisions.

Section 24:6I-48 - Medical cannabis - additional regulatory requirements.

Section 24:6I-49 - Business treatment of cannabis establishments, distributors, and delivery services.

Section 24:6I-50 - Cannabis regulatory, enforcement assistance, and marketplace modernization fund.

Section 24:6I-51 - Licensee and consumer protections.

Section 24:6I-52 - Employers, driving, minors and control of property.

Section 24:6I-53 - Contract enforceability.

Section 24:6I-54 - Federal and interstate relations.

Section 24:6I-55 - Limitations.

Section 24:6I-56 - Severability.

Section 24:6J-1 - Short title.

Section 24:6J-2 - Findings, declarations relative to overdose prevention.

Section 24:6J-3 - Definitions relative to overdose prevention.

Section 24:6J-4 - Immunity from liability for certain prescribers, practitioners, dispensers.

Section 24:6J-5 - Overdose prevention information.

Section 24:6J-5.1 - Provision of certain information to victims of opioid overdoses; definitions.

Section 24:6J-6 - Awarding of grants.

Section 24:6J-7 - Opioid antidotes, recognized place of public access.

Section 24:6K-1 - Definitions relative to dispensing certain biological products.

Section 24:6K-2 - Link to current lists of all biological products.

Section 24:6K-3 - Conditions for substitution.

Section 24:6K-4 - Rules, regulations.

Section 24:6L-1 - Short title.

Section 24:6L-2 - Findings, declarations relative to epinephrine auto-injectors.

Section 24:6L-3 - Definitions relative to epinephrine auto-injectors.

Section 24:6L-4 - Authorization to administer.

Section 24:6L-5 - Written standards, application procedures.

Section 24:6L-6 - Immunity from civil liability, disciplinary action.

Section 24:6L-7 - Construction of act.

Section 24:6M-1 - Findings, declarations relative to drug donation.

Section 24:6M-2 - Definitions relative to drug donation.

Section 24:6M-3 - Establishment, maintenance of drug donation program.

Section 24:6M-4 - Conditions relative to program.

Section 24:6M-5 - Immunity from liability.

Section 24:6M-6 - Construction of act.

Section 24:6M-7 - Rules, regulations.

Section 24:6M-8 - Tax credit for donor.

Section 24:6M-9 - Tax credit for donor.

Section 24:6N-1 - Current wholesale acquisition cost information provided quarterly; non-compliance, penalties; definitions.

Section 24:8-1 - "Caustic acids" and "caustic alkalies" enumerated

Section 24:8-2 - Labeling containers of caustic acids and alkalies intended for household use

Section 24:9-21 - Definitions

Section 24:9-22 - Application for license for refrigerated warehouse or locker plant

Section 24:9-23 - License fees; suspension or revocation of license

Section 24:9-24 - Reports to commissioner

Section 24:9-25 - Notice of insanitary condition of warehouse or locker plant

Section 24:9-26 - Duration of storage period; extension

Section 24:9-27 - Disposition and sale of articles in refrigerated warehouse longer than two years without extension

Section 24:9-28 - Restorage after release from storage prohibited

Section 24:9-29 - Transfer between refrigerators

Section 24:9-30 - Requirements for storage

Section 24:9-31 - Lot numbers for identification

Section 24:9-32 - Marking and tagging of articles placed in storage

Section 24:9-33 - Alteration, mutilation or destruction of tags or marks prohibited

Section 24:9-34 - Penalties for violations

Section 24:9-35 - Enforcement of provisions

Section 24:9-36 - Plaintiff entitled to penalties

Section 24:9-37 - Repeal

Section 24:10-57.1 - Definitions

Section 24:10-57.2 - Permit to operate milk plant or as bulk milk hauler; necessity; transferability; expiration

Section 24:10-57.3 - Restrictions in permits

Section 24:10-57.4 - Temporary or emergency permits

Section 24:10-57.5 - Annual fee; amounts

Section 24:10-57.6 - Preliminary findings

Section 24:10-57.7 - Forms; establishment by state department

Section 24:10-57.8 - Revocation of permit; grounds; renewal; suspension pending hearing

Section 24:10-57.9 - Maintenance of records; inspection

Section 24:10-57.10 - Powers of local board of health

Section 24:10-57.11 - Inconsistent ordinances, rules or regulations

Section 24:10-57.12 - Notification of violations; prohibition of distribution and sale

Section 24:10-57.13 - Inspections; authorized inspectors

Section 24:10-57.14 - Place of inspection

Section 24:10-57.15 - Inability of local board to make inspections

Section 24:10-57.16 - Bacteriological and other tests; methods, techniques, personnel, etc.

Section 24:10-57.17 - Pasteurization required

Section 24:10-57.18 - Milk and fluid milk products; pasteurization

Section 24:10-57.19 - Enforcement; failure of local board to act; procedure by state department

Section 24:10-57.20 - Rules and regulations

Section 24:10-57.21 - Sanitary conditions; health and habits of personnel

Section 24:10-57.22 - Use of apparatus, containers, equipment, etc., for other purposes prohibited

Section 24:10-57.23 - Container regulations

Section 24:10-57.24 - Cans, packages and other containers enclosing milk, milk products or fluid milk products; labelling

Section 24:10-57.24a - Use of or reference to fluid milk product or dairy farm by imitation product; prohibition

Section 24:10-57.24b - Additional rules and regulations for milk products and their imitations

Section 24:10-57.26 - Failure of milk or milk products to meet minimum requirements

Section 24:10-57.27 - Milk and milk products of violators barred from state

Section 24:10-57.28 - Contamination of milk

Section 24:10-57.29 - Severability

Section 24:10-57.30 - Repeals

Section 24:10-73.1 - Rules and regulations of department of health; establishment of standards of identity and definitions

Section 24:10-73.1a - Compliance with rules and regulations; extensions of time

Section 24:10-73.2 - "Frozen desserts" ; definition

Section 24:10-73.5 - Definitions.

Section 24:10-73.6 - Sale of adulterated frozen desserts prohibited

Section 24:10-73.7 - When frozen desserts deemed adulterated

Section 24:10-73.10 - License to sell, distribute frozen desserts.

Section 24:10-73.11 - Form of application; affidavit

Section 24:10-73.12 - Issuance of license; expiration

Section 24:10-73.13 - Revocation or suspension of license; renewal

Section 24:10-73.14 - Illegal sale and distribution of frozen dessert

Section 24:10-73.15 - Use of license moneys for enforcement

Section 24:10-73.16 - Inspection; fee

Section 24:10-73.17 - Partial invalidity

Section 24:10-73.18 - Repeals

Section 24:10A-1 - Straws, tubes and other devices for drinking

Section 24:10A-2 - Rules and regulations

Section 24:10A-3 - Penalty

Section 24:10A-4 - Effective date

Section 24:11-1 - License; expiration

Section 24:11-2 - Revocation of license

Section 24:11-3 - Eggs unfit for food

Section 24:11-4 - Labeling "rots" and "spots"

Section 24:11-5 - Denatured eggs; labeling

Section 24:11-6 - Inspection of egg establishments

Section 24:11-7 - Distribution, sale, etc., of eggs removed from incubators

Section 24:11-8 - Penalty for violation

Section 24:11-9 - Enforcement of act

Section 24:11A-1 - Short title

Section 24:11A-2 - Declaration of purpose

Section 24:11A-3 - Definitions

Section 24:11A-4 - Flour; vitamin and mineral content; minimum standards

Section 24:11A-5 - Bread and rolls; vitamin and mineral content; minimum standards

Section 24:11A-6 - Enrichment; ingredients

Section 24:11A-7 - Modification of vitamin and mineral requirements; interstate commerce; authority of department

Section 24:11A-8 - Shortage of vitamins and minerals; temporary suspension of minimum standards; authority of department

Section 24:11A-9 - Enforcement of act; investigations and inspections

Section 24:11A-10 - Violations; penalties; recovery; disposition

Section 24:11A-11 - Separate violations

Section 24:11A-12 - Actions to restrain violations

Section 24:11A-13 - Repeal of conflicting acts; saving clause

Section 24:11A-14 - Effective date

Section 24:12-1 - "Nonalcoholic drink" defined

Section 24:12-2 - Prohibited adulterations; drinks containing water treated with fluorides

Section 24:12-4 - False advertising

Section 24:12-5 - Licensing of wholesale bottlers

Section 24:12-6 - Issuance of license; period of

Section 24:12-7 - Revocation or suspension of license

Section 24:12-8 - Definitions

Section 24:12-9 - State regulations, standards for bottled water.

Section 24:12-10 - Periodic testing

Section 24:12-11 - Potability test results to Department of Health; annual report to legislative committees

Section 24:12-12 - Procedures, rules, regulations

Section 24:12-13 - Powers of commissioner

Section 24:12-14 - Violations; penalties

Section 24:14A-1 - Use on toys, furniture or accessible surfaces of dwelling; prohibition

Section 24:14A-2 - Toys or furniture; sale or transfer for profit or knowingly transfer or exchange; prohibition

Section 24:14A-3 - Violations; disorderly persons

Section 24:14A-4 - Definitions

Section 24:14A-5 - Lead paint upon interior of building or exterior surface accessible to children; public nuisance

Section 24:14A-6 - Responsibilities of board; enforcement, reports.

Section 24:14A-7 - Order for remediation, disposition of lead-based paint hazard.

Section 24:14A-8 - Notification to owner of hazard, contents.

Section 24:14A-8.1 - Eviction of occupants to avoid corrective maintenance

Section 24:14A-9 - Failure of owner to obey notice or order to abate; removal of nuisance; payment of expenses by owner; action to collect; lien

Section 24:14A-10 - Nonenforcement by board; enforcement by department

Section 24:14A-11 - Rules and regulations by department

Section 24:14B-1 - Sale of paint or coating removal product containing methylene chloride; conditions, violations, penalties.

Section 24:15-1 - Definitions

Section 24:15-2 - Cleanliness, lighting, plumbing and ventilation

Section 24:15-3 - Construction of walls and floors

Section 24:15-4 - Cleanliness of walls, floors, furniture and machinery; use of hydrocyanic acids or salts; running water; multi-use utensils

Section 24:15-5 - Protection of food, drugs or cosmetics from contamination; removal of refuse

Section 24:15-6 - Clothing of employees to be kept clean

Section 24:15-7 - Toilet facilities for and personal cleanliness of employees

Section 24:15-8 - Expectoration prohibited

Section 24:15-9 - Sleeping in rooms of food establishment

Section 24:15-10 - Persons affected with communicable disease

Section 24:15-11 - Order to abate violation in lieu of prosecution

Section 24:15-12 - Furnishing and posting abstract of law

Section 24:15-13 - License; necessity; fee; exemptions

Section 24:15-14 - Fee for license or inspection.

Section 24:15A-1 - Equipment of lead, cadmium, or metallic substance; formation of dangerous compounds; unwholesome, dangerous or detrimental

Section 24:15A-2 - Penalties; recovery and enforcement

Section 24:15A-3 - Packaging of meat

Section 24:15A-4 - Applicability of act; enforcement

Section 24:16B-1 - Short title

Section 24:16B-2 - Declaration of policy

Section 24:16B-3 - Definitions

Section 24:16B-4 - Transfer of authority from Department of Health to Department of Agriculture; general power of Department of Agriculture

Section 24:16B-5 - General power of the board; rules and regulations

Section 24:16B-6 - General powers of the secretary

Section 24:16B-7 - Enforcement by municipalities

Section 24:16B-8 - State inspectors, analysts and employees; continuation of former practices and procedures for a period not in excess of 1 year

Section 24:16B-10 - Powers and duties of local inspectors

Section 24:16B-17 - Inspections

Section 24:16B-18 - Disposition of dead animals

Section 24:16B-19 - Diseased or physically impaired animals

Section 24:16B-20 - Antemortem inspections

Section 24:16B-21 - Unauthorized entry of uninspected animals prohibited

Section 24:16B-22 - Separate slaughter of animals found to show symptoms of disease

Section 24:16B-23 - Separate slaughter and preparation of horsemeat

Section 24:16B-24 - Postmortem inspection

Section 24:16B-25 - Inspection mark required before processing

Section 24:16B-26 - Inspection during processing or preparation

Section 24:16B-27 - Inspection required before packaging or shipment

Section 24:16B-28 - Condemnation; disposition

Section 24:16B-29 - Disposition of by-products

Section 24:16B-30 - Actions authorized

Section 24:16B-31 - Handling, transporting and storing

Section 24:16B-32 - Packaging

Section 24:16B-33 - Contents of labels

Section 24:16B-34 - Registration of labels, marks

Section 24:16B-35 - Sale or shipment of mislabeled packages prohibited

Section 24:16B-36 - Sale or shipment of unwholesome meat prohibited

Section 24:16B-37 - Acceptance by handler-distributor of unwholesome meat prohibited

Section 24:16B-38 - Sale or shipment of horsemeat prohibited

Section 24:16B-39 - Vehicle permits

Section 24:16B-40 - Display of vehicle permits required

Section 24:16B-41 - Other applications of this act

Section 24:16B-42 - Exemption from inspection

Section 24:16B-43 - Removal of inspectors

Section 24:16B-44 - Engaging in business prohibited after removal of inspectors

Section 24:16B-45 - Acts of agents, servants and employees

Section 24:16B-46 - Books and records; rights of entry, inspection of premises

Section 24:16B-47 - Reports of licensee

Section 24:16B-48 - Proceedings before the secretary

Section 24:16B-49 - Hearing procedures

Section 24:16B-50 - Issuance of subpoenas

Section 24:16B-51 - Service of subpoenas; fees and mileage

Section 24:16B-52 - Refusal to obey subpoena or testify; contempt

Section 24:16B-53 - Oaths

Section 24:16B-54 - Grounds for denying license

Section 24:16B-55 - Informal hearings on violations; adjustment

Section 24:16B-56 - Orders of the secretary; service

Section 24:16B-57 - Records of the secretary; reports to the Attorney General

Section 24:16B-58 - Disposition of license fees, penalties, fines and costs

Section 24:16B-59 - Review by Superior Court

Section 24:16B-60 - Violations

Section 24:16B-61 - Actions to restrain violations

Section 24:16B-62 - Co-operation with United States Government

Section 24:16B-63 - Agreements with other agencies

Section 24:16B-64 - Grant of specific powers not to impair general powers

Section 24:16B-65 - Foreign or interstate commerce

Section 24:16B-66 - Authority of department of health not abrogated or affected except as authorized by this act

Section 24:16B-67 - Authority of the division of weights and measures not abrogated or affected

Section 24:16B-68 - Liberal construction

Section 24:16B-69 - Inconsistent acts and rules and regulations superseded

Section 24:16B-70 - Partial invalidity

Section 24:16B-71 - Repeal

Section 24:17-1 - Penalties

Section 24:17-2 - Different places or days as separate violations

Section 24:17-3 - Payment of penalty equivalent to conviction

Section 24:17-4 - Action to restrain violation

Section 24:17-5 - Recovery of penalties; enforcement

Section 24:17-8 - Disposition of penalties collected

Section 24:21-1 - Short title

Section 24:2I-2 - Definitions.

Section 24:21-3 - Authority to control.

Section 24:21-4 - Schedules of controlled substances

Section 24:21-5 - Schedule I.

Section 24:21-6 - Schedule II.

Section 24:21-7 - Schedule III.

Section 24:21-8 - Schedule IV.

Section 24:21-8.1 - Schedule V.

Section 24:21-9 - Rules and regulations.

Section 24:21-10 - Registration requirements.

Section 24:21-11 - Registration.

Section 24:21-12 - Denial, revocation, or suspension of registration.

Section 24:21-13 - Records of registrants.

Section 24:21-14 - Order forms.

Section 24:21-15 - Prescriptions.

Section 24:21-15.1 - Prescriber to discuss risks of dependence on certain drugs with certain patients.

Section 24:21-15.2 - Limitation on amount of opioid initially prescribed under certain circumstances.

Section 24:21-15.3 - Rules, regulations.

Section 24:21-16 - Form of label on containers of manufacturers and wholesalers; altering or removing label.

Section 24:21-17 - Form of label to be used by pharmacists; altering or removing label.

Section 24:21-21 - Prohibited acts C.--Records and order forms of registered manufacturers and distributors--Penalties

Section 24:21-22 - Prohibited acts D.--Fraud or misrepresentation by registered manufacturers or distributors--penalties.

Section 24:21-23 - General penalty

Section 24:21-24 - Attempt, endeavor and conspiracy

Section 24:21-25 - Additional penalties

Section 24:21-29 - Second or subsequent offenses

Section 24:21-31 - Powers of enforcement personnel.

Section 24:21-32 - Administrative inspections and warrants.

Section 24:21-33 - Injunctions

Section 24:21-34 - Cooperative arrangements.

Section 24:21-35 - Nuisances

Section 24:21-36 - Reports of convictions of manufacturers and practitioners.

Section 24:21-37 - Burden of proof; liabilities; immunity

Section 24:21-38 - Judicial review.

Section 24:21-40 - Pending proceedings

Section 24:21-42 - Uniformity of interpretation

Section 24:21-43 - Severability

Section 24:21-44 - Study of penalties relating to use and possession of marihuana

Section 24:21-45 - Repealer

Section 24:21-52 - Seizure in violation of act

Section 24:21-53 - Severability

Section 24:21-54 - "Controlled Dangerous Substances Administration and Enforcement Fund."

Section 24:21-55 - "Project Medicine Drop" program.

Section 24:21-56 - Rules, regulations.