SITCSection 5
U.S. imports of provitamin and vitamin intermixtures (SITC 54117) totaled $6.3M in April 2026, traded with 31 countries.
Importers of Provitamin and Vitamin Intermixtures paid $25K in duties in April 2026 — an effective duty rate of 11% on $230K in dutiable value, based on actual customs collections rather than the published tariff schedule. Provitamin and Vitamin Intermixtures imports of $6.3M in April 2026 ran 23% below the year-to-date monthly average of $8.1M.
Last updated: April 2026 dataPremixed vitamin preparations — including multi-vitamin blends, provitamin combinations, and natural concentrates containing multiple vitamin fractions — are classified here rather than under the individual vitamin headings, making the mixture composition the decisive classification criterion. These intermixtures are widely used as premix inputs for animal feed, infant formula, and dietary supplement manufacturing, where consistent potency and stability across multiple active ingredients are critical quality parameters. FDA oversight applies to human-use grades, and USDA may have jurisdiction over feed-grade premixes depending on the intended animal species. Because potency and blend ratios vary widely, importers should ensure that certificates of analysis accompany each shipment and that the declared composition matches the entry documentation.
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A vitamin intermixture classified here is typically a bulk blend of vitamin actives or provitamins intended as an ingredient for further manufacturing — not a finished, consumer-ready dosage form. Finished tablets, capsules, or softgels presented for retail sale are generally classified under pharmaceutical or food preparation headings. The key factors are presentation (bulk vs. unit dose), packaging, and whether the product is intended for further processing.
Feed-grade vitamin premixes intended for use in animal nutrition are subject to FDA's Center for Veterinary Medicine (CVM) oversight, which regulates animal food ingredients under the Federal Food, Drug, and Cosmetic Act. Importers should ensure that feed-grade premixes are manufactured under conditions consistent with FDA's current Good Manufacturing Practice (cGMP) requirements for animal food and that ingredient safety documentation is available for review.
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| Country | Imports | Exports | Balance |
|---|---|---|---|
| CANADA | $29K | $7.0M | +$7.0M |
| CHINA | $2.0M | $4.0M | +$2.1M |
| UNITED KINGDOM | $96K | $2.2M | +$2.1M |
| NETHERLANDS | -- | $1.4M | +$1.4M |
| SWITZERLAND | $1.3M | -- | -$1.3M |
Monthly import values over time