Himalaya Wellness Company
Prodotti per il benessere a base di erbe supportati dalla scienza in 106 paesi.
Fondata nel 1930, Himalaya Wellness Company è una multinazionale indiana che produce oltre 500 prodotti erboristici per la salute e la cura della persona, combinando la tradizione ayurvedica con la moderna ricerca farmaceutica. I suoi prodotti, tra cui la formula di punta Liv.52 per il fegato e la gamma di prodotti per la cura della pelle Herbals, sono venduti in 106 paesi attraverso filiali negli Stati Uniti, in Europa, nel Medio Oriente e nel Sud-Est asiatico. L'azienda dispone di impianti di produzione in India e Malesia certificati secondo gli standard GMP e ISO per una fornitura internazionale senza interruzioni.
- Type
- brand seeking distribution
- Location
- Bengaluru, India
- Founded
- 1930
- Website
- himalayawellness.in
- Categories
- Skincare e cosmetici, Forniture medicali e sanitarie
- Markets
- Stati Uniti, Germania, Regno Unito, Emirati Arabi Uniti, Australia, Sudafrica, Malaysia, Singapore, Giappone
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)