Himalaya Wellness Company
Productos de bienestar a base de hierbas respaldados por la ciencia en 106 países.
Fundada en 1930, Himalaya Wellness Company es una multinacional india que fabrica más de 500 productos de cuidado personal y sanitario a base de hierbas, combinando la tradición ayurvédica con la investigación farmacéutica moderna. Sus productos, incluida la fórmula insignia para el hígado Liv.52 y la gama de cuidado de la piel Herbals, se venden en 106 países a través de oficinas subsidiarias en EE. UU., Europa, Medio Oriente y el Sudeste Asiático. La empresa mantiene instalaciones de fabricación en India y Malasia certificadas según las normas GMP e ISO para un suministro internacional fluido.
- Type
- brand seeking distribution
- Location
- Bengaluru, India
- Founded
- 1930
- Website
- himalayawellness.in
- Categories
- Cuidado de la piel y cosmética, Suministros médicos y sanitarios
- Markets
- Estados Unidos, Alemania, Reino Unido, Emiratos Árabes Unidos, Australia, Sudáfrica, Malasia, Singapur, Japón
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
- lei-active (green), checked 2026-08-30 GLEIF global LEI register (golden copy)
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
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)