Vitamin E and its derivatives
Vitamin E and its derivatives, provitamin concentrates
HSN 2936 28 00 (Vitamin E and its derivatives) is subject to Food Safety and Standards Authority of India (FSSAI) Import Licence requirements under the Food Safety and Standards Act, 2006, alongside Narcotic Drugs and Psychotropic Substances (NDPS) import-certificate controls under Chapter VII-A of the NDPS Rules, 1985 where scheduled substances are involved. The Directorate General of Foreign Trade (DGFT) ITC (HS) policy condition 2 of Chapter 29 and mandatory Chapter 29 additional qualifiers under CBIC Circular 23/2023-Cus apply as further clearance requirements.
- Import Licence from FSSAI
- Registration certificate from CDSCO/drugs authority
- Certificate of Analysis from supplier
Procedural directions for customs clearance are issued by: Directorate General of Foreign Trade, Central Board of Indirect Taxes and Customs.
- 1Upload all mandatory e-Sanchit documents before filing the bill of entry: Certificate of Analysis — Drug (document code 0010dc), Batch Release Certificate (0030dc), Label of Consignment (0110dc), Specimen Copy of Label (0110fs), Registration Certificate for Drugs (101dc1), FSSAI Import Licence (911001), and Import Licence for Drugs (9111dc). The proper officer will verify these codes before granting out-of-charge.CCR mandatory document list · CBIC e-Sanchit OOC verification requirement
- 2Where any component of the consignment constitutes an NDPS substance, obtain an import certificate under Rule 53 of the NDPS Rules, 1985 (Chapter VII-A) for medical or scientific purposes, or confirm the consignment is governed by Appendix-I to the ITC (HS) Schedule under ITC (HS) policy condition 2 of Chapter 29.ITC (HS) policy condition 2 to Chapter 29 · Rule 53 of the NDPS Rules, 1985
- 3Comply with CBIC Circular 23/2023-Cus dated 30-09-2023 by including mandatory additional qualifiers in the import declaration for Chapter 29 commodities as stipulated in paragraphs 4.1 and 4.2, with effect from 15 October 2023. Declarations without the required qualifiers will be rejected at the bill-of-entry stage.CBIC Circular 23/2023-Cus dated 30-09-2023 · General Note 4(D) of Schedule I of ITC (HS) 2022
The most common error on this tariff line is treating Vitamin E as a food-only product and uploading only the FSSAI Import Licence, while ignoring the parallel drug-registration and NDPS document suite. Where the product is classified as a nutraceutical, health supplement, or medicinal preparation, the Registration Certificate for Drugs (101dc1), Batch Release Certificate (0030dc), and Import Licence for Drugs (9111dc) are independently mandatory; absence of any one of these document codes in e-Sanchit triggers detention at the designated port regardless of FSSAI clearance.