Printed
Printed aluminium foil not exceeding 0.2 mm thickness
HSN 7607 19 95 (printed aluminium foil, not backed, not exceeding 0.2 mm thickness) is covered by two Bureau of Indian Standards Quality Control Orders. 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; printed aluminium foil for pharmaceutical packaging must additionally conform to IS 16011:2012 under the Aluminium and Aluminium Alloy Products (Quality Control) Order, 2025 with effect from 01 October 2025. No separate customs-clearance overlay applies beyond the BIS QCO obligation.
- 1Source only from a Bureau of Indian Standards CM/L-licensed manufacturer holding a current licence against IS 15392. Verify the supplier's CM/L number, licensed product scope, and licensed manufacturing facility on the BIS online register before placing the purchase order.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 printed aluminium foil is destined for pharmaceutical packaging, verify the supplier also holds a current CM/L licence against IS 16011:2012. This obligation took effect from 01 October 2025 for non-micro enterprises and from 01 January 2026 for small enterprises; micro enterprises as defined under the Micro, Small and Medium Enterprises Development Act, 2006 have until 01 April 2026.Aluminium and Aluminium Alloy Products (Quality Control) Order, 2025 · S.O. 2021(E) dated 05-05-2025
- 3Ensure every reel or sheet of printed aluminium foil bears the ISI mark and the supplier's CM/L number in accordance with Scheme-I of Schedule-II of the BIS (Conformity Assessment) Regulations, 2018. Marking must appear on the product or its innermost label, not on the outer packaging 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 supplier's BIS CM/L number on the bill of entry. Where the foil is for pharmaceutical packaging, quote the IS 16011:2012 CM/L separately. Customs verifies each CM/L against the BIS register in real time; an absent, expired, or scope-mismatched licence triggers consignment detention, demurrage, and potential re-export.Aluminium Foil (Quality Control) Order, 2020 · S.O. 687(E) dated 13-02-2020 · BIS Act, 2016 · Customs Act, 1962
- 5For pharmaceutical-packaging foil consignments, confirm whether the exemptions in paragraph 2 of S.O. 2021(E) apply. If an exemption is claimed, retain documentary evidence supporting that basis before the goods arrive at port.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 assuming that a single CM/L against IS 15392 covers all end-use applications. Printed aluminium foil destined for pharmaceutical packaging is now subject to a second, independent QCO obligation — IS 16011:2012 under S.O. 2021(E) — with its own phased effective dates and a separate CM/L requirement. Importers who ship mixed consignments (part general packaging, part pharma packaging) under a single IS 15392 CM/L face detention on the pharma-grade portion regardless of the general packaging licence being current and in scope.