Himalaya Wellness Company
Science-backed herbal wellness products in 106 countries.
Founded in 1930, Himalaya Wellness Company is an Indian multinational that manufactures over 500 herbal healthcare and personal care products, combining Ayurvedic tradition with modern pharmaceutical research. Its products, including the flagship Liv.52 liver formula and the Herbals skincare range, are sold in 106 countries through subsidiary offices in the US, Europe, the Middle East, and Southeast Asia. The company maintains manufacturing facilities in India and Malaysia certified to GMP and ISO standards for seamless international supply.
- Type
- Manufacturer
- Location
- Bengaluru, India
- Founded
- 1930
- Website
- himalayawellness.in
- Categories
- Skincare & Cosmetics, Medical & Healthcare Supplies
- Markets
- United States, Germany, United Kingdom, United Arab Emirates, Australia, South Africa, Malaysia, Singapore, Japan
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- web-presence-since (green), checked 2026-08-08 Internet Archive (Wayback)
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- product-authorised-for-sale (green), checked 2026-08-21 Ministry of Health of Armenia, State Register of Medicinal Products (pharm.am)
- domain-registered (green), checked 2026-08-08 Domain registry record
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
Claimed certifications
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
- EAC mark (EAEU conformity) EAEU unified register of certificates and declarations
Import rules for these goods
- 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)
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)