Kerala Ayurveda Ltd
Kerala Ayurveda Ltd manufactures classical Ayurvedic medicines, herbal wellness products and prop…
Kerala Ayurveda Ltd manufactures classical Ayurvedic medicines, herbal wellness products and proprietary formulations from its GMP-certified plant in Aluva, Kochi. The product range covers oils, capsules, tablets, syrups and personal care items rooted in authentic Ashtangahridayam texts. Wholesale buyers and international distributors access an 800+ SKU catalogue backed by WHO-GMP certification, stability studies and export-ready dossiers tailored for European Herbal Directive and US Dietary Supplement regulations.
- Type
- Manufacturer
- Location
- Kochi, India
- Founded
- 1945
- Website
- keralaayurveda.biz
- Categories
- Medical & Healthcare Supplies, Skincare & Cosmetics
- Markets
- United States, Germany, United Kingdom, United Arab Emirates, Australia
Verified facts
- debarment-clear (green), checked 2026-08-08 OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-08 OpenSanctions
- export-registered (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
- registered-manufacturer (green), checked 2026-08-21 Pharmexcil member directory (Pharmaceuticals Export Promotion Council of India, Ministry of Commerce)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- domain-registered (green), checked 2026-08-08 Domain registry record
Claimed certifications
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
- Halal Certified
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)