Turnkey Supplement Manufacturing
Turnkey supplement manufacturing means one partner takes your product from concept to finished, sellable goods: formula development, raw-material sourcing, production, packaging, labeling compliance and logistics. YUKANG — the brand of Yukang Medicine (Guangzhou) Co., Ltd. — offers turnkey programs from its 10,000 m² cGMP facility in Guangzhou, with North America DDP fulfillment through Yukang Medicine USA and its California warehouse.
What "Turnkey" Actually Includes
Formula development. Start with a product idea, a target consumer or a competitor benchmark. The team of 30+ formulators develops the formula, drawing on the company's self-described library of more than 10,000 formulas and 62 ready-made YJN/RT profiles as starting points. You approve the final profile before production.
Sourcing and production. Raw materials are sourced, verified and tested on intake; production runs on ten fully automatic lines across seven dosage forms — softgels, hard capsules, tablets, gummies, powders, oral drops and oral liquids — under cGMP (21 CFR Part 111).
Packaging and compliance. Bottle, pouch, blister or sachet packaging with your branding; label review for FDA compliance when the destination is the United States; Amazon FBA preparation including labeling, poly-bagging and carton standards.
Logistics. Export documentation and freight, with DDP delivery for North American customers via the California warehouse (established 2025) — the goods arrive duty-paid, FBA-ready, without you acting as importer of record.
Who Turnkey Suits
Turnkey fits brand owners who want to focus on marketing and sales rather than supply-chain management: Amazon sellers launching a first product, distributors entering the supplement category, and established brands adding a new format without qualifying another factory. Because the whole chain sits with one accountable partner, there is a single point of contact from the first sample to the delivered pallet.
Quality and Certification Backbone
The Guangzhou facility operates under cGMP (21 CFR Part 111) and holds FDA food facility registration (a facility registration, not a product certification), ISO 22000 and HACCP; the group's Wuxi site is BRCGS-audited at grade A. Certificates are available upon request. Current export regions include North America, Europe, the Middle East (GCC), Asia-Pacific and Africa.
Timelines and Minimums
Turnkey doesn't mean slow. Samples are typically ready in 7–10 days and standard production completes in about 15 days after sample approval, with MOQs starting at 500–1,000 units — so even a fully custom, from-scratch product can reach a test market quickly.
The Turnkey Process
- Brief & NDA — share your product concept through the upcoming inquiry form and WhatsApp channels (currently being set up — enabled before launch); response within 24 hours, NDA from the first exchange.
- Formula proposal — the formulation team proposes a formula profile for your approval.
- Sampling — samples in 7–10 days.
- Production — about 15 days, with in-process and finished-product QC.
- Packaging, compliance & delivery — labeling, FBA prep, export logistics and North America DDP.
Frequently Asked Questions
I only have a product idea, no formula. Can you still help? Yes — that's exactly what turnkey is for. The formulation team develops the formula from your brief.
Do you handle Amazon FBA requirements? Yes. FBA preparation and FDA labeling compliance support are standard parts of turnkey programs.
How is my concept protected? NDA protection is available from the first exchange, and your formula and brand information are treated as confidential throughout.
Start With a Concept, End With a Product
Describe the product you want to sell — format, target consumer, market — and the team will return a formula proposal and project plan within 24 hours.