Embossed
Embossed aluminium foil not exceeding 0.2 mm thickness
HSN 7607 19 92 (embossed aluminium foil, not backed, not exceeding 0.2 mm thickness) is covered by a Bureau of Indian Standards Quality Control Order. Conformity to IS 15392 is mandatory under the ISI Mark Scheme with effect from 13 February 2020 under the Aluminium Foil (Quality Control) Order, 2020; aluminium and aluminium alloy foil for pharmaceutical packaging must additionally conform to IS 16011:2012 with effect from 01 October 2025 under the Aluminium and Aluminium Alloy Products (Quality Control) Order, 2025. No separate customs-clearance overlay applies beyond the BIS obligations.
- 1Verify the foreign manufacturer holds a current BIS CM/L licence against IS 15392 on the BIS online register before placing the purchase order. Confirm the licensed scope covers embossed aluminium foil at the alloy grade, temper, and thickness range of the consignment.Aluminium Foil (Quality Control) Order, 2020 · S.O. 687(E) dated 13-02-2020 · Scheme-I of Schedule-II of the BIS (Conformity Assessment) Regulations, 2018
- 2If the foil is destined for pharmaceutical packaging, separately verify that the manufacturer holds a CM/L licence against IS 16011:2012. This obligation is active from 01 October 2025 for non-micro enterprises and from 01 April 2026 for micro enterprises as defined under the Micro, Small and Medium Enterprises Development Act, 2006.Aluminium and Aluminium Alloy Products (Quality Control) Order, 2025 · S.O. 2021(E) dated 05-05-2025
- 3Ensure every roll or consignment unit bears the ISI mark and the manufacturer's CM/L number under Scheme-I of Schedule-II to the BIS (Conformity Assessment) Regulations, 2018. Marking must appear on the product or its primary packaging — not on the outer shipping carton alone.Scheme-I of Schedule-II of the BIS (Conformity Assessment) Regulations, 2018 · Aluminium Foil (Quality Control) Order, 2020 · S.O. 687(E) dated 13-02-2020
- 4Quote the manufacturer's BIS CM/L number (and IS 16011:2012 CM/L number where pharmaceutical packaging is the declared end-use) on the bill of entry. Customs verifies the CM/L in real time against the BIS register; an absent, expired, or scope-mismatched licence triggers consignment detention.BIS Act, 2016 · Customs Act, 1962 · S.O. 687(E) dated 13-02-2020 · S.O. 2021(E) dated 05-05-2025
- 5Review the exemption provisions in paragraph 2 of the Aluminium and Aluminium Alloy Products (Quality Control) Order, 2025 before import if the consignment may qualify. Document the exemption basis in writing and retain it with the import file for customs audit.Aluminium and Aluminium Alloy Products (Quality Control) Order, 2025 · S.O. 2021(E) dated 05-05-2025 · para 2 exemptions
The most common error on this tariff line is treating IS 15392 as the sole applicable standard and overlooking IS 16011:2012 when the foil is sold for pharmaceutical packaging. Both Quality Control Orders operate concurrently from 01 October 2025; a consignment declared as pharmaceutical-grade foil without a valid IS 16011:2012 CM/L — even where an IS 15392 CM/L is in order — faces detention under the 2025 Order. Importers should confirm the declared end-use with the buyer before the purchase order, not at the bill-of-entry stage.