Yunnan Baiyao Group Co., Ltd.
Yunnan Baiyao Group is China's most iconic Traditional Chinese Medicine manufacturer, headquarter…
Yunnan Baiyao Group is China's most iconic Traditional Chinese Medicine manufacturer, headquartered in Kunming. The group exports a wide range of herbal health products including the renowned Baiyao powder and plasters, hair-care lines and OTC wound-healing products. Wholesale B2B supply available for TCM distributors, pharmacy chains and health retailers with product registration support for target markets. GMP certified per China NMPA standards. Active in US, Canada, Germany, Australia and Singapore markets.
- Type
- Manufacturer
- Location
- Kunming, China
- Founded
- 1902
- Website
- yunnanbaiyao.com
- Categories
- Medical & Healthcare Supplies, Haircare & Styling
- Markets
- United States, Germany, Australia, Singapore, Canada
Verified facts
- domain-registered (green), checked 2026-08-10 Domain registry record
- corporate-mail-on-domain (green), checked 2026-08-10 Mail server of the company domain
- facility-registered (green), checked 2026-08-19 BPOM (Indonesian Food and Drug Authority), public register of manufacturing facilities behind product registrations (Sarana)
- sanctions-clear (green), checked 2026-08-10 OpenSanctions
- debarment-clear (green), checked 2026-08-10 OpenSanctions
Claimed certifications
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
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)