China Supplement Manufacturer for Global Brands
Reduce unit costs with our verified China factory network — a 50-acre smart factory with 200+ health food approvals and 5,000+ ready-to-use formulas. We manage sampling, production, export documents and delivery so overseas brands scale profitably.
Significant cost advantage
Access large-scale capacity and thousands of formulas to lower your cost per unit.
Full dosage-form range
Softgels, hard capsules, powders, granules, beverages, candy and oral liquids.
Export-ready documents
COA, COO and Free Sale support coordinated for your destination market.
Regulatory snapshot
Key compliance requirements for United States
Governing authority
FDA — 21 CFR Part 111 (cGMP)
Product classification
Dietary Supplement (DSHEA)
Registration / notification
No pre-market approval. Facility must have FDA Food Facility Registration. New dietary ingredients require an NDI notification 75 days before marketing.
Labeling requirements
- "Supplement Facts" panel (not Nutrition Facts)
- Statement of identity + net quantity
- Full ingredient list incl. 'other ingredients'
- Name & place of business of manufacturer/distributor
- DSHEA disclaimer if structure/function claims are used
Typical documents
- FDA Facility Registration number
- cGMP (21 CFR 111) evidence
- Certificate of Analysis (COA)
- Allergen statement
Claims
Structure/function claims allowed with disclaimer; disease claims are prohibited.
Notes
Prop 65 warnings may apply for California distribution.
General reference only, not legal advice. We confirm current rules per product and destination market.
Core capabilities
Built for brands that need to test, iterate and scale
We combine low-MOQ manufacturing, new nutrition delivery technology, formula development and compliance support into one managed supply-chain path.
Fast initial project review
Turn a product brief into an initial manufacturing direction covering formula status, dosage form, packaging, documents and the next decisions needed for a usable quote.
Low MOQ, sampling and trial production
Coordinate project-specific sampling and trial production. The USD 2,000 sample development fee is credited to a subsequent bulk order; production MOQ is confirmed after the formula, format and packaging are reviewed.
Documented multi-location production resources
Coordinate suitable resources in Shanghai, Hong Kong and Singapore, with one project team managing formula review, packaging, applicable documents and delivery planning.
New nutrition delivery technologies
Coordinate cocrystal, microencapsulation, nano and liposomal technology paths to improve stability, taste and bioavailability.
Herbal and compound formula capability
Combine Asian botanical extracts with mainstream Western nutrition ingredients to build differentiated formulas for target audiences.
International project coordination
Use practical experience supporting established supplement brands across different dosage forms and production requirements to reduce communication gaps during development and scale-up.
Our factories and partner lines
A documented manufacturing network across three production regions
We coordinate production through long-term factory partners and hold ownership interests in selected partner facilities. The applicable production route is confirmed for each project.
Entity note: Hangzhou Hengyang Technology Co., Ltd. manages commercial communication and the project. When the Shanghai route is selected, Shanghai Yaoshenfeng Biotechnology Co., Ltd. is the manufacturing entity for formula review, production and applicable documents.
A clear manufacturing route
The applicable manufacturing entity, production location and document path are identified for the project instead of being hidden behind a generic supplier claim.
Direct access to the formulation team
Questions about ingredients, stability or taste go straight to the people running the lines — answers in days, not weeks.
One accountable project team
Formula review, sampling, packaging, applicable documents, production follow-up and delivery planning are coordinated through one team.
Invested manufacturing partnerShanghai, China
Shanghai Yaoshenfeng Biotechnology
Jinshan District, Shanghai
- An invested Shanghai manufacturing partner supporting supplement production, product development, documentation and customized packaging.
- Tablets, softgels, vegetarian softgels, hard capsules, gelatin and vegetarian capsules, powder and liquid formats.
- Private label and packing available on site.
- Documented NSF GMP for Dietary Supplements, HACCP and GRMA qualification references are available for review.
Invested manufacturing partnerHong Kong
BoSang Yotta Solutions Pharmaceutical Factory
Kwai Tsing District, Hong Kong — manufacturing, packing and document support
- An invested Hong Kong manufacturing partner for capsules, softgels, powders, tablets, health foods, confectionery products and solid drinks.
- The facility supports formulation, manufacturing, packing and documentation for multiple supplement dosage forms.
- The natural choice when a buyer needs Hong Kong origin, Hong Kong warehouse delivery, cross-border ecommerce dispatch or flexible trade documentation.
- FEHD food factory licence, U.S. FDA facility registration, FSSC 22000, ISO 22000, HACCP, GMP and SGS on-site audit references.
Additional documented production partners
Singapore
Documented production partnerDocumented manufacturing partners — Singapore
Kim Sin Medicine Manufactory and Harmony Pharma Lab provide documented Singapore production resources that may be mobilized when the project and product category fit.
Certificates and documents are provided where applicable, depending on facility and destination market. On-site and video factory audits are welcome.