ARC 35K - State Compliance

ARC 35K | Built for North Carolina Compliance

Session Law 2024-31 PMTA Registry Information

✓ State Confirmation

What is ARC 35K?

ARC 35K is a non-nicotine device designed for today's evolving regulatory landscape. Built to deliver a familiar experience without using nicotine or tobacco-derived ingredients, ARC provides a forward-thinking alternative for retailers and consumers alike.

Instead of nicotine, ARC utilizes Hypertine, a proprietary compound not derived from tobacco or traditional nicotine sources. This positions ARC within a different category than conventional nicotine products, making it a strong option in markets with increasing regulatory pressure.

Regulatory Overview

ARC does not contain nicotine and is not derived from tobacco. As a result, it falls outside of the definitions that typically trigger nicotine-based regulatory requirements under current North Carolina law.

North Carolina regulates vapor products through Session Law 2024-31, which establishes a PMTA registry system governing which nicotine-containing products may be sold in the state. This framework is focused on products that contain nicotine and require FDA authorization, PMTA submission, or inclusion in the state registry.

Product classification (particularly nicotine content) plays a central role in determining how products are regulated.

What Changes

North Carolina's implementation of a PMTA registry represents a shift toward stricter control of nicotine-containing vapor products. Retailers and distributors must ensure that applicable products are listed within the registry to remain compliant.

As enforcement increases, non-compliant nicotine products are being removed from shelves, and retailers are shifting toward more stable and compliant inventory options.

Products like ARC, which do not contain nicotine, are generally positioned outside traditional nicotine classifications.

✔ Allowed Products

  • PMTA-authorized or pending products listed in the registry
  • Products under appeal or with a stay
  • Non-nicotine vapor products
  • Products not derived from tobacco
  • Hardware (devices without nicotine)

ARC falls within the non-nicotine category described above.

Why This Matters for Retailers

  • North Carolina's registry system has significantly narrowed the range of nicotine products that can be legally sold in the state.
  • Retailers must ensure their inventory aligns with current registry requirements to avoid disruption.
  • ARC is built for this shift, offering retailers a more reliable option in an increasingly regulated market.

Stay Ahead of Compliance Changes

Stock products designed for where the market is going, not where it's been. Carry with confidence. Sell with certainty.

This content is for informational purposes only and does not constitute legal advice. Regulations and enforcement may vary and are subject to change.

ARC 35K | Built for Mississippi Compliance

Mississippi Regulatory Compliance Information

✓ State Confirmation

What is ARC 35K?

ARC 35K is a non-nicotine device designed for today's evolving regulatory landscape. Built to deliver a familiar experience without using nicotine or tobacco-derived ingredients, ARC provides a forward-thinking alternative for retailers and consumers alike.

Instead of nicotine, ARC utilizes Hypertine, a proprietary compound not derived from tobacco or traditional nicotine sources. This positions ARC within a different category than conventional nicotine products, making it a strong option in markets with increasing regulatory pressure.

Regulatory Overview

ARC does not contain nicotine and is not derived from tobacco. As a result, it falls outside of the definitions that typically trigger nicotine-based regulatory requirements under current Mississippi law.

Mississippi regulates vapor products based on whether they contain nicotine or are derived from tobacco. Products classified as Electronic Nicotine Delivery Systems (ENDS) are subject to certification and regulatory requirements tied to nicotine content and federal authorization standards.

Product classification (particularly nicotine content) plays a central role in determining how products are regulated.

What Changes

Retailers and distributors in Mississippi are facing increased scrutiny around the sale of nicotine-containing vape products, particularly those without FDA authorization or PMTA status. As enforcement increases, non-compliant nicotine products are being removed from shelves, and retailers are shifting toward safer, more reliable inventory.

Products like ARC, which do not contain nicotine, are generally positioned outside traditional nicotine classifications.

✔ Allowed Products

  • PMTA-authorized or pending products
  • Products under appeal or with a stay
  • Non-nicotine vapor products
  • Products not derived from tobacco
  • Hardware (devices without nicotine)

ARC falls within the non-nicotine category described above.

Why This Matters for Retailers

  • State enforcement is increasing, and non-compliant products are being removed from shelves across the country.
  • Retailers are shifting toward inventory they can confidently carry without disruption.
  • ARC is built for this shift, offering retailers a more reliable option in an increasingly regulated market.

Stay Ahead of Compliance Changes

Stock products designed for where the market is going, not where it's been. Carry with confidence. Sell with certainty.

This content is for informational purposes only and does not constitute legal advice. Regulations and enforcement may vary and are subject to change.

ARC 35K | Built for Kentucky Compliance

Kentucky Regulatory Compliance Information

✓ State Confirmation

What is ARC 35K?

ARC 35K is a non-nicotine device designed for today's evolving regulatory landscape. Built to deliver a familiar experience without using nicotine or tobacco-derived ingredients, ARC provides a forward-thinking alternative for retailers and consumers alike.

Instead of nicotine, ARC utilizes Hypertine, a proprietary compound not derived from tobacco or traditional nicotine sources. This positions ARC within a different category than conventional nicotine products, making it a strong option in markets with increasing regulatory pressure.

Regulatory Overview

ARC does not contain nicotine and is not derived from tobacco. As a result, it falls outside of the definitions that typically trigger nicotine-based regulatory requirements under current Kentucky law.

Kentucky regulates vape products through a combination of federal alignment and state-level enforcement, with a focus on nicotine-containing products and their compliance with FDA authorization requirements.

Unlike some states, Kentucky does not currently maintain a centralized vape product registry or directory.

Product classification (particularly nicotine content) plays a central role in determining how products are regulated.

What Changes

Retailers in Kentucky must ensure that nicotine-containing vape products comply with applicable federal and state requirements, including FDA authorization where applicable.

As enforcement evolves, products without clear compliance status may face increased scrutiny.

Products like ARC, which do not contain nicotine, are generally positioned outside traditional nicotine classifications.

✔ Allowed Products

  • PMTA-certified or pending products
  • Products under appeal or with a stay
  • Zero-nicotine e-liquids
  • Nicotine analogs
  • Hardware (devices without nicotine)

ARC falls within the non-nicotine category described above.

Why This Matters for Retailers

  • State enforcement is evolving, and retailers are under increasing pressure to ensure the products they carry align with both federal and state expectations.
  • Without a centralized registry system, product classification becomes even more important.
  • ARC is built for this environment, offering a non-nicotine option that provides greater flexibility and reduced regulatory risk.

Stay Ahead of Compliance Changes

Stock products designed for where the market is going, not where it's been. Carry with confidence. Sell with certainty.

This content is for informational purposes only and does not constitute legal advice. Regulations and enforcement may vary and are subject to change.

ARC 35K | Built for Arkansas Compliance

Arkansas Regulatory Compliance Information

✓ State Confirmation

What is ARC 35K?

ARC 35K is a non-nicotine device designed for today's evolving regulatory landscape. Built to deliver a familiar experience without using nicotine or tobacco-derived ingredients, ARC provides a forward-thinking alternative for retailers and consumers alike.

Instead of nicotine, ARC utilizes Hypertine, a proprietary compound not derived from tobacco or traditional nicotine sources. This positions ARC within a different category than conventional nicotine products, making it a strong option in markets with increasing regulatory pressure.

Regulatory Overview

ARC does not contain nicotine and is not derived from tobacco. As a result, it falls outside of the definitions that typically trigger nicotine-based regulatory requirements under current Arkansas law.

Arkansas regulates vape products with a focus on nicotine-containing devices and their compliance with federal PMTA (Premarket Tobacco Product Application) requirements.

Products that contain nicotine or are classified under tobacco product definitions are subject to stricter oversight, including certification and enforcement measures.

Product classification (particularly nicotine content) plays a central role in determining how products are evaluated.

What Changes

Retailers in Arkansas must ensure that nicotine-containing vape products comply with applicable federal PMTA requirements and state-level enforcement standards.

As enforcement increases, non-compliant nicotine products may face removal from shelves or distribution restrictions.

Products like ARC, which do not contain nicotine, are generally positioned outside traditional nicotine classifications.

✔ Allowed Products

  • PMTA-certified or pending products
  • Products under appeal or with a stay
  • Non-nicotine vapor products
  • Products not derived from tobacco
  • Hardware (devices without nicotine)

ARC falls within the non-nicotine category described above.

Why This Matters for Retailers

  • State enforcement is increasing, and non-compliant nicotine products are being removed from shelves across the country.
  • Retailers are shifting toward inventory they can confidently carry without disruption.
  • ARC is built for this shift, offering a more reliable option in an increasingly regulated market.

Stay Ahead of Compliance Changes

Stock products designed for where the market is going, not where it's been. Carry with confidence. Sell with certainty.

This content is for informational purposes only and does not constitute legal advice. Regulations and enforcement may vary and are subject to change.

ARC 35K | Built for Virginia Compliance

Virginia Regulatory Compliance Information

✓ State Confirmation

What is ARC 35K?

ARC 35K is a non-nicotine device designed for today's evolving regulatory landscape. Built to deliver a familiar experience without using nicotine or tobacco-derived ingredients, ARC provides a forward-thinking alternative for retailers and consumers alike.

Instead of nicotine, ARC utilizes Hypertine, a proprietary compound not derived from tobacco or traditional nicotine sources. This positions ARC within a different category than conventional nicotine products, making it a strong option in markets with increasing regulatory pressure.

Regulatory Overview

ARC does not contain nicotine and is not derived from tobacco. As a result, it falls outside of the definitions that typically trigger nicotine-based regulatory requirements under current Virginia law.

Virginia regulates vapor products based on whether they contain nicotine or are derived from tobacco. Products that contain liquid nicotine or are designed to deliver nicotine through inhalation fall within the state's regulatory framework and may be subject to additional requirements, including directory inclusion and excise taxation.

Product classification (particularly nicotine content) plays a central role in determining how products are evaluated.

What Changes

Virginia's regulatory approach is based on how products are defined under existing law, particularly with respect to nicotine content.

Retailers must determine whether a product falls within the state's definition of a nicotine vapor product when assessing compliance.

Products like ARC, which do not contain nicotine, are generally positioned differently from traditional nicotine classifications.

✔ Allowed Products

  • Non-nicotine vapor products
  • Products not derived from tobacco
  • Products outside Virginia's nicotine classification

ARC falls within the non-nicotine category described above.

Why This Matters for Retailers

  • Virginia's regulations are driven by product definitions, making it essential for retailers to understand how products are classified under the law.
  • Carrying products that fall outside nicotine definitions may reduce regulatory complexity and risk.
  • ARC provides a non-nicotine option aligned with this framework, helping retailers make more informed and compliant decisions.

Stay Ahead of Compliance Changes

Stock products designed for where the market is going, not where it's been. Carry with confidence. Sell with certainty.

This content is for informational purposes only and does not constitute legal advice. Regulations and enforcement may vary and are subject to change.

ARC 35K | Listed in Louisiana's Directory

Louisiana Vape Directory Compliance

✓ Directory Listed

What is ARC 35K?

ARC 35K is a non-nicotine device designed for today's evolving regulatory landscape. Built to deliver a familiar experience without using nicotine or tobacco-derived ingredients, ARC provides a forward-thinking alternative for retailers and consumers alike.

Instead of nicotine, ARC utilizes Hypertine, a proprietary compound not derived from tobacco or traditional nicotine sources. This positions ARC within a different category than conventional nicotine products, making it a strong option in markets with increasing regulatory pressure.

Regulatory Overview

ARC does not contain nicotine and is not derived from tobacco. As a result, it falls outside of the definitions that typically trigger nicotine-based regulatory requirements under current Louisiana law.

Louisiana maintains a state-run vape product directory that determines which products are approved for sale within the state. Only products listed within the Louisiana Vape Directory are authorized for legal sale and distribution.

As a result, inclusion in the directory is the primary requirement for retailers operating within Louisiana.

What Changes

Retailers in Louisiana must ensure that all vape products they carry are listed within the official Louisiana Vape Directory.

Products not included in the directory are not permitted for sale.

Louisiana Vape Directory Listing

ARC is included in the official Louisiana Vape Directory. Retailers can verify this listing directly through the state directory.

Louisiana Directory

This provides clear, verifiable confirmation of ARC's listing.

✔ Allowed Products

  • Products listed in the Louisiana Vape Directory

ARC meets this requirement and is listed accordingly.

Why This Matters for Retailers

  • Louisiana has one of the most clearly defined compliance frameworks, where only listed products are permitted for sale.
  • Retailers must be confident that every product they carry is included in the state directory.
  • ARC's verified listing helps retailers operate with clarity and reduced risk.

Stay Ahead of Compliance Changes

Stock products designed for where the market is going, not where it's been. Carry with confidence. Sell with certainty.

This content is for informational purposes only and does not constitute legal advice. Regulations and enforcement may vary and are subject to change.

ARC 35K | Built for Nebraska Compliance

Nebraska Directory Compliance

What is ARC 35K?

ARC 35K is a non-nicotine device designed for today's evolving regulatory landscape. Built to deliver a familiar experience without using nicotine or tobacco-derived ingredients, ARC provides a forward-thinking alternative for retailers and consumers alike.

Instead of nicotine, ARC utilizes Hypertine, a proprietary compound not derived from tobacco or traditional nicotine sources. This positions ARC within a different category than conventional nicotine products, making it a strong option in markets with increasing regulatory pressure.

Regulatory Overview

ARC does not contain nicotine and is not derived from tobacco. As a result, it falls outside of the definitions that typically trigger nicotine-based regulatory requirements under current Nebraska law.

Nebraska maintains a state directory that determines which vapor products are authorized for sale. Only products listed on the Nebraska Directory of Certified Electronic Nicotine Delivery Systems (ENDS) Manufacturers are permitted to be sold within the state.

This means that product eligibility for sale in Nebraska is determined entirely by directory inclusion.

Product classification (particularly nicotine content) plays a central role in determining how products are evaluated under this framework.

What Changes

Retailers in Nebraska must ensure that all vapor products they carry are included in the official state directory. Products not listed on the directory are not authorized for sale.

This creates a strict compliance environment where directory status must be verified before products are stocked or sold.

Products that fall outside nicotine classifications may be evaluated differently depending on how the directory framework is applied.

Directory Status

Nebraska requires that vapor products be included on the state directory prior to sale.

ARC is currently in the process of being submitted for inclusion on the Nebraska Directory of Certified Electronic Nicotine Delivery Systems (ENDS) Manufacturers, as part of ongoing regulatory alignment efforts.

Listing status should be verified through the official state directory, as product eligibility is determined by inclusion at the time of sale.

✔ Allowed Products

  • Products listed on the Nebraska state directory
  • Products that meet state certification requirements

Only products included in the directory are authorized for sale.

Why This Matters for Retailers

  • Nebraska has a clearly defined compliance system where only listed products are permitted for sale.
  • Retailers must be confident that every product they carry is approved at the state level and included on the official directory.
  • Understanding and verifying listing status is critical to avoiding regulatory risk.
  • ARC is designed for today's evolving regulatory landscape, and its directory status should be confirmed as part of standard compliance review.

Stay Ahead of Compliance Changes

Stock products designed for where the market is going, not where it's been. Carry with confidence. Sell with certainty.

This content is for informational purposes only and does not constitute legal advice. Regulations and enforcement may vary and are subject to change.

ARC 35K | Built for Pennsylvania Compliance

Pennsylvania Regulatory Compliance Information

✓ State Confirmation

What is ARC 35K?

ARC 35K is a non-nicotine device designed for today's evolving regulatory landscape. Built to deliver a familiar experience without using nicotine or tobacco-derived ingredients, ARC provides a forward-thinking alternative for retailers and consumers alike.

Instead of nicotine, ARC utilizes Hypertine, a proprietary compound not derived from tobacco or traditional nicotine sources. This positions ARC within a different category than conventional nicotine products, making it a strong option in markets with increasing regulatory pressure.

Regulatory Overview

ARC does not contain nicotine and is not derived from tobacco. As a result, it falls outside of the definitions that typically trigger nicotine-based regulatory requirements under current Pennsylvania law.

Pennsylvania regulates tobacco products and electronic cigarettes based on whether they contain nicotine or are derived from tobacco. Products that contain liquid nicotine or are classified as tobacco products are subject to regulation, including excise taxation and other compliance requirements.

Product classification (particularly nicotine content) plays a central role in determining how products are regulated.

What Changes

Pennsylvania's regulatory approach is based on how products are currently defined under existing law, rather than upcoming regulatory changes. The key consideration for retailers is whether a product contains nicotine or falls within the state's definition of a tobacco or nicotine product.

Non-nicotine vapor products may still be subject to regulation if they are marketed under the same brand family as nicotine-containing products. This distinction can impact how products are evaluated under state law.

Products like ARC, which do not contain nicotine, are generally positioned outside traditional nicotine classifications.

✔ Allowed Products

  • Non-nicotine vapor products
  • Products not derived from tobacco
  • Products outside Pennsylvania's nicotine and tobacco classifications

ARC falls within the non-nicotine category described above.

Why This Matters for Retailers

  • Pennsylvania's regulations are driven by product definitions and taxation, making it essential for retailers to understand how products are classified under the law.
  • Carrying products that clearly fall outside nicotine and tobacco definitions, and are not associated with nicotine-containing product brand families, can reduce regulatory risk and simplify compliance considerations.
  • ARC provides a non-nicotine option aligned with Pennsylvania's regulatory framework, giving retailers clarity and confidence.

Stay Ahead of Compliance Changes

Stock products designed for where the market is going, not where it's been. Carry with confidence. Sell with certainty.

This content is for informational purposes only and does not constitute legal advice. Regulations and enforcement may vary and are subject to change.

ARC 35K | Built for Colorado Compliance

Colorado Regulatory Compliance Information

✓ State Confirmation

What is ARC 35K?

ARC 35K is a non-nicotine device designed for today's evolving regulatory landscape. Built to deliver a familiar experience without using nicotine or tobacco-derived ingredients, ARC provides a forward-thinking alternative for retailers and consumers alike.

Instead of nicotine, ARC utilizes Hypertine, a proprietary compound not derived from tobacco or traditional nicotine sources. This positions ARC within a different category than conventional nicotine products, making it a strong option in markets with increasing regulatory pressure.

Regulatory Overview

ARC does not contain nicotine and is not derived from tobacco. As a result, it falls outside of the definitions that typically trigger nicotine-based regulatory requirements under current Colorado law.

Colorado regulates tobacco products and vapor products based on whether they contain nicotine or are derived from tobacco. Products that contain nicotine are subject to excise taxation and additional regulatory requirements under Colorado law.

In addition to state law, several municipalities in Colorado have enacted local restrictions on flavored vapor products, which may apply independently of statewide regulations. These local rules are often more restrictive and must be considered alongside state requirements.

What Changes

Colorado's regulatory structure is not based on upcoming changes, but on how products are currently defined and taxed under existing law. The key consideration for retailers is whether a product contains nicotine or falls within the state's definition of a taxable nicotine or tobacco product.

Products like ARC, which do not contain nicotine, are generally positioned outside traditional nicotine classifications.

✔ Allowed Products

  • Non-nicotine vapor products
  • Products not derived from tobacco
  • Products outside Colorado's nicotine and tobacco classifications

ARC falls within the non-nicotine category described above.

Why This Matters for Retailers

  • Colorado's regulations are closely tied to nicotine classification and excise taxation, making it essential for retailers to understand how products are defined under the law.
  • Carrying products that fall outside nicotine classifications may reduce exposure to certain nicotine-based tax and regulatory requirements.
  • However, retailers must also account for local municipal restrictions, which may impose additional limitations depending on location.
  • ARC provides a non-nicotine option aligned with Colorado's regulatory framework.

Stay Ahead of Compliance Changes

Stock products designed for where the market is going, not where it's been. Carry with confidence. Sell with certainty.

This content is for informational purposes only and does not constitute legal advice. Regulations and enforcement may vary and are subject to change.

ARC 35K | Built for New York Compliance

New York Regulatory Compliance Information

✓ State Confirmation

⚠ Disclaimer: Compliancy does not apply to New York City

What is ARC 35K?

ARC 35K is a non-nicotine device designed for today's evolving regulatory landscape. Built to deliver a familiar experience without using nicotine or tobacco-derived ingredients, ARC provides a forward-thinking alternative for retailers and consumers alike.

Instead of nicotine, ARC utilizes Hypertine, a proprietary compound not derived from tobacco or traditional nicotine sources. This positions ARC within a different category than conventional nicotine products, making it a strong option in markets with increasing regulatory pressure.

Regulatory Overview

ARC does not contain nicotine and is not derived from tobacco. As a result, it falls outside of the definitions that typically trigger nicotine-based regulatory requirements under current New York law.

New York prohibits the sale of flavored vapor products that contain nicotine under Public Health Law Article 13-F.

Guidance from the New York State Department of Health indicates that products containing non-nicotine ingredients may be treated differently, provided they are not intended for use with nicotine products.

Product classification (particularly nicotine content and intended use) plays a central role in determining how products are evaluated.

What Changes

Retailers in New York must ensure that products they carry do not contain nicotine and are not marketed for use with nicotine products.

Products that fall outside of nicotine classifications may be treated differently under current enforcement guidance.

ARC, as a non-nicotine product, aligns with this framework.

State Guidance

The New York State Department of Health has issued formal guidance indicating that flavored vapor products containing non-nicotine ingredients may fall outside the scope of Public Health Law Article 13-F, when not intended for use with nicotine products.

This guidance reinforces the distinction between nicotine and non-nicotine products within New York's regulatory framework.

Application of this guidance may depend on product characteristics, labeling, and intended use.

✔ Allowed Products

  • Non-nicotine vapor products
  • Products not intended for use with nicotine
  • PMTA-certified or authorized nicotine products

ARC falls within the non-nicotine category described above.

Why This Matters for Retailers

  • New York is one of the most restrictive vapor markets in the country, with strict limitations on flavored nicotine products.
  • Retailers must carefully evaluate how products are classified and marketed under current law and guidance.
  • ARC aligns with state guidance, supporting informed, lower-risk decisions.

Stay Ahead of Compliance Changes

Stock products designed for where the market is going, not where it's been. Carry with confidence. Sell with certainty.

This content is for informational purposes only and does not constitute legal advice. Regulations and enforcement may vary and are subject to change.