Other, containing vitamins or other products of heading 2936: — Containing vitamins synthesized wholly or in part from aromatic or modified aromatic industrial organic compounds:
H253927 · 2014-11-20 — Application for Further Review of Protest No. 4701-13-100387; Tariff Classification of Ergocalciferol Capsules
This protest involves eleven (11) entries made between 2012 and 2013 of Ergocalciferol Capsules, under the Harmonized Tariff Schedule of the United States (HTSUS). Our response follows. FACTS: The Ergocalciferol capsules at issue are a mixture of Ergocalciferol, soybean oil, gelatin, glycerol, water, and coloring. They are imported in bulk in 1.25mg doses, or 50,000 international units (IU). Swiss Caps originally entered the subject merchandise under heading 2936, HTSUS, which provides for pro-vitamins, but it was later rate advanced by the Port of John F. Kennedy International Airport, and…
H121544 · 2014-10-06 — Application for Further Review Protest No. 1101-10-100060; Tariff classification of dietary medical products.
(”Nutricia”). The Protest is against U.S. Customs and Border Protection’s (“CBP”) classification of dietary medical products under heading 2106 of the Harmonized Tariff Schedule of the United States (“HTSUS”). We have also considered arguments presented by counsel on April 8, 2013, to members of my staff. FACTS: The articles at issue in this AFR are described as dietary medical products, which are also called “medical foods.” These items are: Neocate 1+ (aka Neocate One +): a nutritionally complete powdered amino acid-based food. Prepared for consumption by mixing with water. Neocate Junior:…
083000 · 1990-09-19 — Tariff Classification of Analog XP, Maxamaid XP, Maxamum XP
This is in reference to your submission on the classification under the Harmonized Tariff Schedule of the United States (HTSUS) of phenylalanine-free dietary preparations. FACTS: The products are powdered dietary formulations specifically formulated to satisfy the dietary restrictions for a patient suffering from phenylketonuria (PKU). PKU is a metabolic disorder characterized by an inability to convert phenylalanine, an essential amino acid which can not be synthesized by the body and is necessary for survival, into tryosine, an amino acid essential for the PKU patient. If the phenylalanine…
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