About Yukang Medicine
A Strategic Supply Chain Partner for Global Supplement Brands
Founded in 2015 as an international dietary supplement trading enterprise, Yukang Medicine grew into a full-service contract manufacturer with a 10,000 m² cGMP cleanroom facility, ten fully automated production lines — and since 2025, a US subsidiary and local warehouse for North American fulfillment.
- Legal entity
- Yukang Medicine (Guangzhou) Co., Ltd.
- Founded
- 2015 — Guangzhou, Guangdong, China
- Manufacturing base
- Building 2, No. 43, Lixin 9th Road, Zengcheng District, Guangzhou, China
- Facility
- 10,000 m² cGMP cleanroom · 10 automated production lines
- Dosage forms
- Softgels, hard capsules, tablets, gummies, powders, oral liquids and oral drops
- Business model
- Private label, OEM and ODM contract manufacturing for supplement brands
- Certifications
- FDA facility registration · cGMP · ISO 22000 · HACCP · BRCGS
- US operation
- US subsidiary and warehouse established 2025 for North American fulfilment
Our Journey
Company Milestones
Global Vision
Founded as an international dietary supplement manufacturer and trading enterprise, building deep expertise in private label supplement services, OEM/ODM supply chain operations, and cross-border logistics for nutraceutical brands entering the global market.
cGMP Manufacturing Facility
Built a 10,000 m² dietary supplement manufacturing facility running to cGMP and launched tablet and powder production lines — registered with the FDA as a food facility and operating ISO 22000 and HACCP food safety systems, with full third-party audit documentation.
Product Expansion
Added hard capsule and oral liquid supplement manufacturing capacity, expanded formulation development services and ingredient sourcing network to serve private label supplement brands across nutraceutical categories.
Gummy Innovation
Introduced pectin and gelatin functional gummy production lines, completing a full dosage-form matrix covering softgels, hard capsules, tablets, gummies, powders, oral drops and oral liquids for both private label and custom formulation.
500+ Brand Partners
Reached 500+ global brand partners in the dietary supplement and nutraceutical industry, supported by an in-house R&D team handling custom formulation development, ingredient qualification and accelerated stability testing programs.
Doubling Scale
Scaled OEM/ODM contract manufacturing capacity to serve 1,000+ overseas supplement brands, with an integrated turnkey supply chain covering custom formulation, contract manufacturing, FDA label compliance and global shipping documentation.
North America Localization
Established a US subsidiary with a California warehouse, enabling fast North American fulfillment, DDP shipping for FDA-regulated dietary supplements, and shorter lead times for private label supplement reorders from US brands.
Mission · Vision · Values
What Drives Us
Mission
Compliance-powered innovation, crafting global health — empowering brands with compliant, high-quality supplement manufacturing.
Vision
To be the world's most trusted strategic partner in dietary supplements.
Values
Service excellence, high efficiency, proactive enterprise and continuous innovation.
Who We Work With
Four Kinds of Buyer, One Production System
Most of the brands we manufacture for arrive at one of four starting points. The commercial model changes; the quality system, the batch documentation and the people do not.
First-Time Brand Owners
You have a product idea, a target market and a launch date, but no formula and no factory. Start from one of 10,000+ stock formulas, keep MOQ at 500–1,000 units, and evaluate free samples in 7–10 days before committing to bulk. Artwork, Supplement Facts and packaging are handled in the same order.
Established Supplement Brands
You already sell, and you are adding a format or moving a line to a second supplier. Seven dosage forms under one roof means a capsule, a stick pack and a gummy launch share one quality system, one deviation process and one set of release criteria instead of three suppliers with three interpretations of cGMP.
Distributors & Own-Label Retailers
You need a range, not a product — consistent labelling across SKUs, a document pack your customers' QA teams will accept, and a supplier who can repeat a batch two years later. Retained samples and batch records are kept for the shelf life of the product for exactly this reason.
E-Commerce & Amazon Sellers
You sell online and the constraint is logistics, not manufacturing. DDP freight, FBA prep with FNSKU and expiry labelling, and a California warehouse for replenishment shorten the distance between a production run and a live listing.
How We Are Different
Four Things That Change the Buying Experience
Seven Formats, One Quality System
Softgels, capsules, tablets, gummies, powders, liquids and drops are produced inside the same 10,000 m² cGMP cleanroom. A multi-format range does not fracture into multiple audits or multiple COA formats.
Formulation Library Plus In-House R&D
30+ formulation specialists working from 10,000+ ready-made formulas. That combination is what makes a two-week launch realistic: most briefs start from something that already exists and has already been stability-tested.
Documentation Before Claims
Specification sheet before production, Certificate of Analysis per batch, stability data behind every shelf-life date, and a published corrective-action process for anything that goes wrong. What we will not do is describe a facility registration as a product approval.
A US Warehouse, Not Just a US Phone Number
Our California subsidiary holds stock and ships DDP domestically in 2–5 business days, which turns a reorder from a six-week ocean cycle into a domestic replenishment. Manufacturing stays in Guangzhou; the last mile does not.
Explore
Where to Go Next
If you are evaluating us as a supplier, these are the four pages that answer the questions a procurement team actually asks.
Services & Commercial Models
Private label, OEM, ODM and turnkey compared on customization, MOQ and lead time — plus the six-step process from inquiry to delivery.
Certifications
What FDA food facility registration does and does not mean, and what each of the other certificates covers — without overstating any of them.
Quality Control
The six-stage control chain from supplier qualification to release, the tests run on every batch, and the documents that come out the other end.
Trust Center
The document pack we release under NDA, three ways to verify us independently, and the claims we deliberately do not make.
Inside Yukang
Our Facility, People & Production Floor
Behind every compliant formula is a cGMP cleanroom, an automated production line and a team of quality specialists. Here is a look inside our 10,000 m² dietary supplement manufacturing facility in Guangzhou, China.
Compliance
Certifications
Our facility is registered with the FDA as a food facility and operates to cGMP, ISO 22000, HACCP and BRCGS standards — full audit documentation is available to brand partners and retailers on request. FDA facility registration is not an FDA approval or certification of any product.