Hindustan Unilever Ltd.
インド最大の日用消費財会社
Hindustan Unilever (HUL) はユニリーバのインド部門で、幅広いホームケア製品、パーソナルケア製品、食品を製造しています。インド全土にある数十の工場では、ラックス、サーフ エクセル、キッサンなどのブランドを国内市場向けに生産しています。 HUL のインドでの生産はすべて、同国の消費者市場に提供されています。
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Mumbai, India
- Founded
- 1931
- Website
- https://www.hul.co.in
- Categories
- パーソナルケア, 飲料
- Markets
- インド
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- domain-registered (green), checked 2026-08-12 Domain registry record
- sanctions-clear (green), checked 2026-08-12 OpenSanctions
- debarment-clear (green), checked 2026-08-12 OpenSanctions
- customer-reviews (amber), checked 2026-08-12 MouthShut
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- lei-active (green), checked 2026-09-07 GLEIF global LEI register (golden copy)
- registered-since (green), effective since 1933-10-17 Company Master Data (Ministry of Corporate Affairs)
- registered-address (green), effective since 2015-03-31 Company Master Data (Ministry of Corporate Affairs)
- registry-activity (green), effective since 2015-03-31 Company Master Data (Ministry of Corporate Affairs)
- cin-on-site (amber), checked 2026-09-17 Published on the company's own website
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management IAF CertSearch
- ISO 22000, Food Safety IAF CertSearch
- HACCP
- EAC mark (EAEU conformity) EAEU unified register of certificates and declarations
Import rules for these goods
- EU imports of food of animal origin and many other food categories must be pre-notified in TRACES and enter through border control posts. European Commission (TRACES)
- US imports require the foreign facility to be FDA-registered and the importer to run a Foreign Supplier Verification Program (FSVP). US FDA
- Cosmetic products must be notified in the EU Cosmetic Products Notification Portal (CPNP) before being placed on the EU market. European Commission (CPNP)
- For the US market, MoCRA requires cosmetic facility registration and product listing with the FDA. US FDA (MoCRA)