SITCSection 0
U.S. imports of vegetable products used chiefly for human food, n.e.s. (SITC 05489) totaled $7.8M in April 2026, traded with 48 countries.
Importers of Vegetable Products Used Chiefly for Human Food, N.E.S. paid $1.9M in duties in April 2026 — an effective duty rate of 26% on $7.5M in dutiable value, based on actual customs collections rather than the published tariff schedule. Vegetable Products Used Chiefly for Human Food, N.E.S. imports of $7.8M in April 2026 ran 21% below the year-to-date monthly average of $9.9M.
Last updated: April 2026 dataFunctioning as a residual catch-all, this heading captures plant-derived food products intended primarily for human consumption that do not fit any more specific SITC vegetable or food category — a classification that demands careful pre-entry review to confirm no named heading applies. Products landing here can range from lesser-known edible botanicals to novel plant-based ingredients, and FDA regulates them as food under standard import admissibility procedures including facility registration and FSMA compliance. The breadth of this heading makes it a frequent subject of CBP classification rulings, and importers should document the product's botanical identity and primary end-use thoroughly.
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Importers should first conduct a thorough classification analysis to confirm the product does not fit a more specific SITC or HTS heading. Obtaining a binding ruling from CBP before the first shipment is advisable for novel or ambiguous products. Supporting documentation should include the product's botanical name, processing description, and intended food use. Consult a licensed customs broker to navigate the classification and FDA admissibility requirements.
FDA applies the same general food import framework — facility registration, FSMA preventive controls, and prior notice — regardless of whether a product falls under a named or residual vegetable heading. However, novel plant-based ingredients may also trigger additional review under FDA's food additive or GRAS (Generally Recognized as Safe) framework if they have not been previously marketed in the US, adding a layer of regulatory complexity beyond standard import admissibility.
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Monthly import values over time