Product directory
The Attorney General maintains a public list of manufacturers and products with submitted certifications. Products offered for retail sale must appear in the directory under the applicable statutory provisions.
Policy resource center
Use this page to understand the current framework, verify claims against official sources, and track dates that matter. This information is for public education and is not legal advice.
The framework
Virginia’s approach combines a state product directory with manufacturer certification, retailer duties, licensing, taxes, and youth-access safeguards.
The Attorney General maintains a public list of manufacturers and products with submitted certifications. Products offered for retail sale must appear in the directory under the applicable statutory provisions.
Manufacturers certify each product and identify the applicable federal marketing-status pathway described in Virginia law. A listing should not be casually described as blanket “FDA approval.”
Virginia rules address licensing, sourcing, recordkeeping, employee education, age verification, inspections, packaging, and penalties.
Paid, submitted, but not necessarily listed
Some manufacturers have made substantial compliance investments, including federal PMTA work and Virginia’s product-by-product fee. But submission and payment alone do not permit a sale: the product must appear in the directory.
Virginia law recognizes a limited pathway for qualifying products with timely federal PMTAs that remain pending. That means a pending federal decision is not automatically the same as ignoring the rules.
The initial certification fee is $2,000 for each product SKU. The Attorney General reported collecting $380,000 from 13 manufacturers by December 31, 2025.
Submitting documents and paying the fee does not itself authorize a product. A product must appear in the public directory before a Virginia retailer may offer it for sale.
Virginia’s public materials do not provide a queue, processing-time dashboard, or product-level status for paid submissions that are not yet listed. Save VA Vapes supports receipts, trackable status, timely decisions, and a fair correction or appeal process.
The Attorney General reported $380,000 collected from 13 manufacturers by December 31, 2025. That confirms manufacturers paid for 190 product certifications at the $2,000 initial fee, but the report does not identify a pending paid queue, processing times, or how many unlisted submissions are complete. Claims about individual delayed products should therefore be documented case by case. Save VA Vapes supports a public status system and timely decisions so compliant applicants are not left in regulatory limbo.
Read the official annual reportCurrent Virginia rules
The identical 2024 measures created a product-by-product certification and directory system. The operative rule is straightforward: a liquid nicotine or nicotine vapor product must be listed before it may be offered for retail sale in Virginia.
Virginia Code § 59.1-293.20 prohibits selling, distributing, importing for resale, or offering a liquid nicotine or nicotine vapor product for retail sale unless it appears in the Attorney General’s directory.
A manufacturer submits a certification and fee for each product SKU. The Attorney General reviews the supporting documentation and maintains the public directory.
A product must have an FDA marketing authorization, or fit the limited pathway for a product marketed by August 8, 2016 with a PMTA submitted by September 9, 2020 that remains under review or has no final decision in effect.
Virginia also requires 21+ sales, identification checks, employee education, lawful sourcing, recordkeeping, packaging safeguards, and taxes. Beginning October 1, 2026, retailers must also obtain a Virginia ABC retail tobacco permit.
Virginia law does not state a categorical flavor ban. Instead, directory eligibility depends on FDA marketing authorization or a limited pathway for certain applications filed by September 9, 2020. Many flavored products cannot satisfy either route and therefore cannot be listed or lawfully sold. Some flavored products may qualify, so the effect is substantial product exclusion rather than a literal ban on every flavored item. Always check the current directory for product-specific status.
Verify before you rely
Use the Attorney General’s page instead of a screenshot, social post, or old spreadsheet.
Check manufacturer, brand, product name, flavor, nicotine strength, and SKU where shown.
FDA marketing-order status is a separate federal question and can change.
Directory entries and agency guidance may be updated. Note when you performed the check.
Enforcement timeline
The directory law, litigation, agency guidance, and 2026 enforcement changes have developed in stages. This timeline reflects official sources available August 2, 2026.
April 17, 2024
The identical 2024 measures created Virginia’s manufacturer-certification and product-directory framework through Chapters 793 and 828 of the Acts of Assembly.
December 31, 2025
The Attorney General published the directory and the statutory deadline for manufacturers to certify products took effect, followed by a 60-day retail inventory period.
April 1, 2026
After litigation initially paused parts of the law, the Fourth Circuit allowed enforcement to move forward. Current Attorney General guidance identifies April 1 as the enforcement start date.
July 30, 2026
The Attorney General announced a Regulated Products Enforcement Unit for directory administration, civil enforcement, retail compliance, education, and coordination.
October 1, 2026
Administration of retail tobacco permits shifts to Virginia ABC, alongside updated statutory provisions.
Source library
Official government sources are listed first. Industry-sponsored economic studies are labeled separately and should not be treated as state forecasts.
Virginia Legislative Information System
One of two identical enacted measures establishing manufacturer certification, the product directory, sales restrictions, and penalties.
Read sourceVirginia Legislative Information System
House companion to SB 550 establishing the 2024 liquid nicotine and nicotine vapor product directory framework.
Read sourceOffice of the Attorney General of Virginia
Official directory access, certification overview, fee information, and enforcement notice.
Read sourceVirginia Legislative Information System
Directory, manufacturer certification, recordkeeping, prohibited sales, enforcement, and effective-date provisions.
Read sourceVirginia Legislative Information System
Retail permit, minimum-age, identification, inspection, and penalty provisions effective October 1, 2026.
Read sourceVirginia Joint Commission on Health Care
State staff review of use, Virginia’s retailer footprint, directory implementation, enforcement capacity, and the 2026 permit framework.
Read sourceOffice of the Attorney General of Virginia
July 30, 2026 announcement describing the unit’s directory, civil-enforcement, compliance, education, and coordination duties.
Read sourceOffice of the Attorney General of Virginia
Reports that 13 manufacturers had certified products and $380,000 in fees had been collected by December 31, 2025. It does not publish a pending-application queue or processing times.
Read sourceVirginia Department of Taxation
Current tax rates and licensing transition information for liquid nicotine products.
Read sourceVirginia General Assembly study materials / Virginia Tax data
Reports an estimated $9,534,881 in FY2024 liquid-nicotine tax due based on filed returns, before dealer discounts, penalties, and interest. It does not separate flavored products.
Read sourceVirginia Department of Taxation
Reports aggregate Other Tobacco Products collections but does not publish a separate flavored-vapor or liquid-nicotine total for FY2025.
Read sourceVirginia Department of Health
Virginia smoking-attributable mortality and health-cost estimates, including the separate estimate for secondhand-smoke deaths.
Read sourceVirginia Department of Health
Virginia estimates produced with CDC’s Alcohol-Related Disease Impact methodology, covering chronic diseases and injuries attributable to excessive alcohol use.
Read sourceVirginia Department of Health
Reports 81 Virginia outbreak cases and one associated death as of November 15, 2019, without publicly identifying the deceased person’s product, substance, flavor, or source.
Read sourceCenters for Disease Control and Prevention
Links most national EVALI cases to THC-containing products, particularly from informal sources, and identifies vitamin E acetate as strongly linked to the outbreak.
Read sourcePreventive Medicine Reports / National cohort study
Peer-reviewed national cohort analysis. It is not Virginia-specific and emphasizes the need for larger samples and longer follow-up.
Read sourceU.S. Food and Drug Administration
Federal marketing-order records and explanation of the premarket tobacco product application pathway.
Read sourceCenters for Disease Control and Prevention
National 2024 youth-use context; not a Virginia-specific estimate.
Read sourceRVA Magazine
A reported retailer perspective on product loss and business viability. It is evidence of local concern, not an official statewide closure count.
Read sourceJohn Dunham & Associates for Vapor Technology Association
Industry-sponsored 2023 economic model covering direct, supplier, and induced jobs, wages, output, and tax contributions. It is not an official Virginia forecast.
Read sourceJohn Dunham & Associates for Vapor Technology Association
Industry-sponsored scenario model estimating potential Virginia employment, wage, output, and state/local tax effects. Results are projections, not observed losses.
Read sourceCommon questions
The statute does not state a categorical flavor ban. It prohibits retail sale of products outside the state directory, and directory eligibility is tied to FDA authorization or a limited pending-application pathway. Because many flavored products cannot satisfy those criteria, the system functions as a de facto restriction on much of the flavored market. Some flavored products may still qualify, so the official directory controls product-by-product status.
It is the Attorney General-maintained list of liquid nicotine and nicotine vapor product manufacturers and products with current certifications submitted under Virginia law.
Not necessarily. Virginia law describes multiple certification pathways and federal status can change. The state directory and FDA marketing-order records should both be checked.
Keeping flavored nicotine vapor products legally available to adults 21+ with no categorical or de facto flavor ban. We support strict age verification, transparent and timely directory decisions, accountable supply chains, workable compliance, and enforcement focused on unlawful sellers.
No. This site provides public education. Businesses should consult official agencies and qualified counsel about their obligations.