Insight | Lower Appeal for Non-Smokers: ARAC, a Behavioral ScienceFirm, Explores Nicotine Pouch Study Under FDA Oversight

Dec.02.2024
ARAC's latest study, presented at CORESTA 2024 under FDA oversight within the PMTA framework, shows nicotine pouches have limited appeal among non-smokers, regardless of flavor. 2Firsts explores how these findings could impact the industry, especially amid challenges in the nicotine pouch market, where competition from compliant tobacco companies, ENDS players, and gray-market products is driving a push for stricter compliance.

By Echo Guo

Co-founder & COO of 2Firsts

 

Editor's Note:

At the CORESTA 2024 Congress, Dr. Jessica Zdinak, Chief Research Officer at ARAC, presented the company's latest research. As a leading global media and consultancy in the NGP industry, 2Firsts was intrigued by the findings and engaged with ARAC to obtain the presentation slides. This article, authored by 2Firsts, is based on those slides and the key insights from ARAC's research, set against the backdrop of current industry trends. lt explores the study's implications for nicotine pouches, their potential impact on public health, and the regulatory landscape.

 

 

In the rapidly evolving market of novel tobacco products, Oral Nicotine Pouches are seen as a promising solution for reducing health risks.

 

According to the latest insights from Verified Industry, the global market for Oral Nicotine Pouches is projected to surge from $1.2 billion in 2023 to $5.5 billion by 2033. Major players in the tobacco industry, including Philip Morris International (PMI) and Altria, have already secured a dominant position in this rapidly expanding market. Meanwhile, e-cigarette companies, particularly those with supply chains in China, are swiftly entering the nicotine pouch space, aiming to capitalize on this growth and increase competition in the sector. As the market heats up, these developments highlight the growing intersection of traditional tobacco products and newer, potentially less harmful alternatives.

 

The United States is currently the largest market for nicotine pouches and serves as a barometer for the global market. While the public is increasingly focused on the potential of nicotine pouches to reduce health risks and their convenience of use, there are growing concerns about their ability to appeal to non-users, particularly teenagers. This category also falls under FDA regulation, which requires companies to conduct TPPI(Tobacco Product Perception and Intention)studies as part of the new tobacco product application process, in accordance with the FDA's CTP.

 

At the CORESTA 2024 Congress, ARAC (Applied Research and Analysis Company) presented a pivotal TPPI study on the public perception of Oral Nicotine White Pouches (ONWP). The study indicates that, compared to smokers, non-users showed lower intentions to try or use ONWP.

 

 

Three Key Takeaways: Making the Case for Oral Nicotine White Pouches

 

 

One of the key conclusions of the study is the comparison of intentions between users and non-users regarding ONWPs. Non-users showed significantly lower intentions to try both flavored and tobacco-flavored ONWPs compared to users. A crucial aspect of the study also addressed whether flavor or tobacco taste was more appealing to non-users. The findings revealed that non-users intentions to try or use ONWPs were similar for both tobacco-flavored and flavored products.

 

Next, regarding relative risk perceptions, both users and non-users perceived the general pouch category, flavored ONWPs, and tobacco-flavored ONWPs as carrying similar levels of health risk. For most participants, the perceived health risk of ONWPs was lower than that of cigarettes, while others considered the risk of using ONWPs to be on par with smoking cigarettes. This suggests that, in terms of risk perception, ONWPs are viewed more favorably.

 

 Insight | Lower Appeal for Non-Smokers: ARAC, a Behavioral ScienceFirm, Explores Nicotine Pouch Study Under FDA Oversight
Intentions to Try ONWPs Among Adult Smokers and Non-Users. Higher scores indicate stronger intention to try| Image source: ARAC

 

Third, Reasons to Use ONWPs highlighted that the primary appeal is the perception of lower harm compared to smoking. Both the user and non-user groups endorsed the belief that "using ONWPs is less harmful to me than smoking" as the strongest reason for use. While the top reasons for using ONWPs varied between groups, this shared perception of reduced harm remained central.

 

 Insight | Lower Appeal for Non-Smokers: ARAC, a Behavioral ScienceFirm, Explores Nicotine Pouch Study Under FDA Oversight
Relative risk perception of nicotine products among adult smokers and non-users | Image source: ARAC

 

 

How ARAC Conducts TPPI on Nicotine Pouches Under FDA Compliance

 

 

The study, conducted in late 2023 (October-November), involved 1,423 U.S. adults, including 432 smokers and 991 non-smokers. Participants were recruited online through a screening process to ensure they met specific inclusion criteria. The study focused on adults aged 21 to 65.

 

 Insight | Lower Appeal for Non-Smokers: ARAC, a Behavioral ScienceFirm, Explores Nicotine Pouch Study Under FDA Oversight
ONWP TPPI Study Groups| Image source: ARAC

 

Three types of oral nicotine white pouches (ONWP) were tested: a general variant, a flavored version, and a tobacco-flavored option. Participants were shown product stimuli before being asked about their intentions to try, use, or switch to the product, as well as their perceptions of the associated risks.

 

The ARAC study was designed to explore two key dimensions:

 

  • Comparing Tobacco Users and Non-Users: The study examined how tobacco users and non-users viewed ONWP products, focusing on their intentions to try and use the product and their risk perceptions.

 

  • Intentions vs. Risk Attitudes: The study assessed both participants' behavioral intentions—whether they would try or continue using ONWP—and their attitudes toward the perceived risks of using such products.

 

 

The Study's Impact: Dissecting Misconceptions, Informing FDA Policy, and Guiding Industry Innovation

 

 

The findings of ARAC's TPPI study represent a pivotal moment in how nicotine pouches are perceived, especially in relation to their appeal to non-smokers. By addressing long-held misconceptions, the research offers a clearer understanding of the role these products might play in harm reduction and public health.

 

The study offers key insights for regulatory decision-making, demonstrating that ONWPs could significantly reduce health risks for smokers while posing minimal risks to non-smokers. This finding aligns with the FDA's Appropriate for the Protection of Public Health (APPH) standard, suggesting that ONWPs may meet the criteria for approval under the PMTA.

 

The study shows that nicotine pouches align with FDA standards, suggesting a quicker shift toward compliance. This could reduce gray-market and counterfeit products, creating a more transparent, regulated market. Companies committed to compliance stand to benefit. Additionally, the finding that flavored pouches are less appealing to non-smokers than tobacco flavors could spur innovation in flavor development, provided it is scientifically validated and meets regulatory standards.

 

 

Study Limitation: The Lack of Adolescent Data

 

 

A limitation of this study is its exclusive focus on adult participants, leaving out a crucial demographic: adolescents. Flavors in tobacco products are widely believed to attract younger users. However, the study’s conclusions—showing that flavors have a weaker appeal for non-smokers compared to smokers—are based solely on adult data. This creates a significant gap, as adolescents, influenced by social and developmental factors, may respond differently to flavored products.

 


 

ARAC BIO

 

Applied Research and Analysis Company (ARAC) is a leading U.S. based behavioral science research firm that designs, executes, and presents scientifically-sound, yet customizable studies to support manufacturers, regulatory agencies, and industry consultants. Their expertise aincludes consumer-focused research services in product development and innovation and regulatory science supporting marketing authorization applications, with SUCCESS in U.S. product authorizations and applications.

 

ARAC specializes in MODULE 5 & 6 studies including: label/claim development and comprehension, human factors/usability testing, and clinical/behavioral studies, such as randomized experimental longitudinal, actual use, TPPI, and post-market surveillance systems.

 

"Most Outstanding Service to Industry" 2024 Golden Leaf award-winning fully staffed IN-HOUSE psychologists, behavioral scientists, statisticians, survey methodologists, and medical monitoring offer tailored research solutions with unparalleled integrity and an exceptional client experience. (Source: ARAC)

 


 

2Firsts is dedicated to reporting on global THR scientific research and fostering deeper and more comprehensive exchanges among science, industry, and regulation. Our mission is to advance the global development of THR initiatives.

 

We welcome article submissions, interview opportunities, or commentary. Please contact us at info@2firsts.com or connect with 2Firsts CEO Alan Zhao on LinkedIn here.

German Customs Seize 115,800 Vapes in €1.4 Million Tax Case
German Customs Seize 115,800 Vapes in €1.4 Million Tax Case
Germany's Magdeburg Main Customs Office seized 115,800 untaxed e-cigarettes containing a combined 4.366 million mL of e-liquid during four truck inspections between August 10 and September 4, 2026. The seizures prevented an estimated €1.397 million in tax losses and set a record for the customs office's jurisdiction. Criminal proceedings have been initiated against four truck drivers. The case follows a separate German investigation involving more than 7.6 million illicit vapes and an estimated €33.3 million in excise-tax losses.
Enforcement
Oct.13
Swedish Match Faces Broader Labeling Order After ZYN Inspection, Documents Obtained by 2Firsts Show
Swedish Match Faces Broader Labeling Order After ZYN Inspection, Documents Obtained by 2Firsts Show
Documents obtained by 2Firsts show that Sweden's Public Health Agency ordered Swedish Match to revise ingredient labels beyond the five ZYN products inspected. The dispute centers on whether flavoring ingredients must be individually disclosed, with Swedish Match citing trade-secret protection and the regulator insisting on full ingredient disclosure. The company faces a conditional penalty of SEK 2 million per month for noncompliance. As of October 22, the agency had received no appeal, despite the company's stated intention to challenge the decision.
Oct.22
Philippines Mandates Safety Certification for Nicotine Pouches, Gives Industry 12 Months to Comply
Philippines Mandates Safety Certification for Nicotine Pouches, Gives Industry 12 Months to Comply
The Philippines Department of Trade and Industry has placed nicotine pouches under mandatory product certification through Department Administrative Order No. 26-07, Series of 2026. Nicotine pouches must obtain a Philippine Standard, or PS, license before they can be manufactured, imported, packed, distributed or sold in the country. The regime requires testing for nicotine content, pH and water activity, while packaging must disclose nicotine strength, ingredients, allergens, batch information, the PS certification mark and prescribed health warnings. Existing market participants have a 12-month transition period to comply.
Regulations
Oct.12
PMI Expands Its Second Global and First Asian Business Services Hub in the Philippines, Serving 160 Markets and Scaling Up AI Capabilities
PMI Expands Its Second Global and First Asian Business Services Hub in the Philippines, Serving 160 Markets and Scaling Up AI Capabilities
Philip Morris International's PMI Business Solutions Philippines has expanded its global business services hub in Makati and plans to add more than 80 positions. Established in 2021 primarily to provide finance and IT support to about 20 markets, the center now employs 519 professionals delivering roughly 600 services across 160 markets. Its functions now span finance, human resources, IT, commercial operations, data analytics, supply chain and project management. PMI says the hub's next phase will focus on AI-enabled and higher-value work. The company did not disclose the size or investment cost of the expansion.
Sep.24
Special Report|From CrossBar 20K to 6-Methyl Nicotine KUMI: Two Routes Into U.S. State Vape Directories?
Special Report|From CrossBar 20K to 6-Methyl Nicotine KUMI: Two Routes Into U.S. State Vape Directories?
Several U.S. states have incorporated the September 9, 2020 PMTA filing deadline into eligibility rules for certain vaping products. CrossBar 20K drew attention after appearing on Pennsylvania's 163-entry directory. A broader 2Firsts investigation found that related registration businesses also listed KUMI and CROSSBAR SIX products, with 171 KUMI-related entries across Louisiana, Nebraska and Wisconsin. Corporate records link Scott Silverman to Blue Nine LLC and VR Products I LLC. PMTA compliance expert Mr. K said historical applications and nicotine-analogue products may offer two different approaches to state-directory access.
Regulations
Oct.26
STIIIZY Redesign Fails to Escape PAX Labs Patent Import Ban as Section 337 Case Also Involves China ALD
STIIIZY Redesign Fails to Escape PAX Labs Patent Import Ban as Section 337 Case Also Involves China ALD
U.S. Customs and Border Protection ruled that STIIIZY had not shown that the redesigned cannabis-vape products covered by its latest request fall outside an ITC limited exclusion order tied to PAX Labs patents. CBP accepted some of STIIIZY’s claim-construction and non-infringement arguments, but the company did not address two additional claims in the same patent. Earlier STIIIZY redesigned cartridges and certain associated components imported with them had received separate CBP clearance.
Sep.16