Regulatory & Licensing Information
Reflexo Homeo Pvt. Ltd. is fully compliant with Indian pharmaceutical regulations governing the manufacture and sale of homoeopathic medicines.
Regulatory Framework
- All products are manufactured in compliance with the Drugs & Cosmetics Act, 1940 and Rules thereunder
- Our homoeopathic medicines are prepared in accordance with the Homoeopathic Pharmacopoeia of India (HPI)
- Manufacturing is carried out under a valid Drug Manufacturing Licence issued by the competent State Licensing Authority of Uttarakhand
Good Manufacturing Practice (GMP)
Our manufacturing facility follows Schedule M-I (GMP norms for homoeopathic medicines) as prescribed under the Drugs & Cosmetics Rules. This includes:
- Controlled manufacturing environment
- In-process and finished product quality testing
- Proper documentation and batch traceability
- Regular internal and third-party audits
Product Classification
All our products are classified as homoeopathic medicines under Indian pharmaceutical law. They are not classified as food supplements, nutraceuticals, or cosmetics.
Important Notice for Consumers
Homoeopathic medicines are regulated in India. These products are not evaluated by the US FDA or equivalent international regulatory bodies. Claims made are based on homoeopathic principles and traditional use.
Contact for Regulatory Enquiries
Reflexo Homeo Pvt. Ltd.
Khasra No. 7 Ch, Mndavar Pragna, Bhagwanpur, Haridwar, Uttarakhand – 247661
Email: sales@reflexohomoeo.com | info@reflexohomoeo.com
Phone: +91 90 70 83 70 70
Website: www.reflexohomeo.com
