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U.S. Market Entry Guide for Food Packaging Manufacturer: Tariffs, FDA Compliance, and 2026 Regulatory Shifts

For any food packaging manufacturer targeting the U.S. market in 2026, the compliance landscape has become significantly more complex. This guide examines tariff classifications, FDA food contact compliance requirements, pending chemical bans, and practical steps for food packaging manufacturer exporters navigating the U.S. market.
Jul 30th,2026 113 Views

01 Tariff Classification and Duty Rates for Food Packaging

For a food packaging manufacturer exporting to the United States, correct HS classification is the foundation of cost predictability. The U.S. Harmonized Tariff Schedule (HTS) distinguishes between two primary categories of paper-based food packaging:

HTS Code Description General Duty Rate
4819.10.00 Corrugated paper/paperboard cartons, boxes, and cases Free (0%) 
4819.10.00.20 Sanitary food and beverage containers (corrugated) Free
4819.20.00.20 Sanitary food and beverage containers (folding cartons, non-corrugated) Free
4819.20.00.20 Folding cartons, boxes, and cases of non-corrugated paper/paperboard Free

Key tariff insights:

  • Paper-based food packaging is duty-free across both corrugated and non-corrugated categories under the 2026 HTS, unaffected by Section 301 or IEEPA tariffs.

  • Plastic packaging (e.g., polyethylene bags with extruded closures) falls under HTS 3923.21.0030, carrying a 3% ad valorem general duty rate, and may be subject to additional Chapter 99 tariffs depending on country of origin.

  • Footnote alert: Both 4819.20.00.20 and 4819.10.00 carry the notation "See 9903.88.03"—which refers to certain tariff exclusions. Exporters should verify whether their specific product falls under any exceptions.

The de minimis suspension: Effective August 29, 2025, Executive Order 14324 suspended the $800 duty-free de minimis exemption for all countries. Low-value packages are now subject to either:

  • A specific duty ($80–$200 per item, depending on country of origin IEEPA rate), available until February 28, 2026; or

  • Ad valorem duty thereafter.

For a food packaging manufacturer shipping samples or small orders, this means even low-value consignments now attract duties, with carriers responsible for calculating and remitting payments.



02 FDA Food Contact Material Compliance: The Baseline Requirement

Any food packaging manufacturer exporting to the U.S. must comply with FDA regulations under Title 21 of the Code of Federal Regulations (21 CFR). Compliance is not optional—it is a legal prerequisite enforced by customs and retail buyers.

Key 21 CFR sections applicable to food packaging:

Regulation Scope
21 CFR Part 176 Paper and paperboard components in contact with food
21 CFR 176.170 Paper/paperboard for aqueous and fatty foods
21 CFR 176.180 Paper/paperboard for dry foods
21 CFR Part 177 Polymers used in plastic food packaging
21 CFR Part 175 Adhesives and coating components
21 CFR Part 174 Good Manufacturing Practice for food contact substances
21 CFR Part 186 Indirect food substances affirmed as GRAS
21 CFR Part 189 Substances prohibited from use in human food

Practical compliance steps:

  1. Material testing: FDA compliance requires third-party lab testing to verify substance content and migration levels. Testing uses simulants that mimic the food type the packaging will contact.

  2. Documentation: A food packaging manufacturer should obtain SGS or Intertek test reports—not just a supplier declaration—demonstrating compliance with the relevant 21 CFR sections.

  3. ISO certification ≠ FDA compliance: ISO 9001 certifies quality management systems, not chemical safety. A food packaging manufacturer must provide material-specific compliance documentation separate from factory certifications.



03 Pending Legislation: The "No Toxic Chemicals in Food Packaging Act of 2026"

On June 9, 2026, identical bills (S. 4724 and H.R. 9231) were introduced in the U.S. Congress that would fundamentally alter the compliance burden for any food packaging manufacturer exporting to the U.S.

Substances that would be deemed "unsafe" for food contact use:

The proposed legislation would ban:

  • Ortho-phthalates

  • PFAS (perfluoroalkyl and polyfluoroalkyl substances)

  • Bisphenol A, B, S, F, AF, and related compounds

  • Acrolein, Acrylamide, BHA

  • Chlorinated paraffins, 1,4-Dioxane

  • Asbestos, Benzene, Chloroform, Methylene chloride

  • Ethylene Oxide, Formaldehyde

  • Styrene Polymers

Critical implications:

  • Styrene polymers: The inclusion of "Styrene Polymers" would effectively ban polystyrene (PS) food packaging—a category widely used for cups, clamshells, and takeout containers.

  • No federal preemption: The bill explicitly states that state and local governments may enforce stricter standards, meaning California's Proposition 65 and state-level PFAS bans would remain in force.

  • Vulnerable populations: When reviewing alternative substances, the FDA would be required to consider impacts on infants, children, pregnant women, the elderly, and workers.

Timeline: The bill is in committee as of July 2026. Passage is not guaranteed, but its introduction signals a clear regulatory trajectory.



04 Additional Regulatory Layers: State Laws, Labeling, and FSMA

Beyond federal FDA rules, a food packaging manufacturer must navigate:

Model Toxics in Packaging Legislation

Adopted by many U.S. states, this restricts:

  • Heavy metals (lead, cadmium, mercury, hexavalent chromium): total concentration ≤ 0.01%

  • Phthalates: ≤ 0.01%

  • PFAS: no detectable level 

Fair Packaging and Labeling Act (FPLA)

Requires disclosure of:

  • Product identity

  • Manufacturer/packer/distributor name and address

  • Net quantity of contents

  • Net quantity of servings 

FSMA Recordkeeping (21 CFR Part 1)

All persons who manufacture, process, pack, transport, or import food in the U.S. must maintain records—including for food contact materials—whether or not the food enters interstate commerce.



05 Who Pays the Tariff? FOB vs. DDP Considerations

For a food packaging manufacturer quoting U.S. buyers, trade terms determine tariff liability:

Term Exporter's Obligation Importer's Obligation
FOB (Free on Board) Export customs clearance Import clearance and all U.S. duties 
CIF/CFR Transport to destination port Import clearance and all U.S. duties 
DDP (Delivered Duty Paid) All export AND import duties None (exporter pays all) 

Critical note: Under FOB terms, a food packaging manufacturer does not pay U.S. import duties—the U.S. buyer does. However, the economic burden often flows back through price negotiations, especially in a tariff-heavy environment . Additional duties under Section 301 or IEEPA remain the obligation of the U.S. importer of record, but may be factored into negotiated pricing .



06 Key Recommendations for Food Packaging Manufacturer Exporters

  1. Audit your material formulations now: If your packaging contains PFAS, phthalates, bisphenols, or styrene polymers, plan for reformulation ahead of potential legislation.

  2. Obtain FDA-compliant lab test reports: Engage SGS, Intertek, or similar accredited labs to test your specific material batches against 21 CFR Parts 176, 177, and 175.

  3. Clarify trade terms in contracts: Specify Incoterms (e.g., FOB Shanghai, CIF Los Angeles) in all sales agreements to avoid tariff disputes.

  4. Factor de minimis changes into sample shipping: With the $800 exemption suspended, budget for duties on sample shipments and small orders.

  5. Monitor federal legislation: The No Toxic Chemicals in Food Packaging Act—if passed—would impose sweeping bans. Stay informed through trade associations and customs brokers.



The window for "business as usual" in food packaging exports to the U.S. is closing. A food packaging manufacturer that proactively aligns with FDA standards and anticipates material bans will be best positioned to maintain market access as regulatory requirements tighten.