Welcome to China's premier industrial hub for high-purity nutraceutical powders and standardized botanical extracts. As an ISO 22000, cGMP, and FDA-registered manufacturer, we deliver end-to-end contract manufacturing, bulk supply, and custom liposomal encapsulation for global dietary supplement brands, pharmaceutical formulators, and functional food innovators.
Explore our clinical-grade, laboratory-tested active nutraceutical ingredients (APIs). Each batch is fully certified with COA, Heavy Metal Screening, and HPLC Purity Analysis.
Standardized Ginsenosides >80% via HPLC. Cultivated via bioreactor tissue culture for zero pesticide residues.
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Endotoxin-free human milk oligosaccharide for infant nutrition, microbiome engineering, and cognitive wellness formulations.
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High-bioavailability metabolic co-factor. Ideal for ATP cellular energy optimization and custom liposomal encapsulation.
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Botanical antioxidant derived from Punica granatum L., engineered for cellular health, anti-glycation, and anti-inflammatory uses.
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Synergistic blend of cold-pressed spirulina, chlorella, wheatgrass, and digestive enzymes with full micronutrient preservation.
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Low molecular weight (<500 Da) enzymatic hydrolysate for rapid intestinal absorption and dermal extracellular matrix synthesis.
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Cold-water dispersible microencapsulated Docosahexaenoic Acid. Odorless formulation for infant, adult, and geriatric supplements.
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Ultra-pure enzymatic synthesis NAD+ precursor. High-density crystal powder optimized for hard-capsule and tablet compression.
Get CatalogThe global nutraceutical industry is experiencing a profound paradigm shift driven by stringent regulatory frameworks, scientific validation demands, and consumer migration toward clean-label bio-actives. According to global market analytics, the market for functional powder raw materials is projected to exceed USD 38.6 Billion by 2030, registering a CAGR of 8.4%.
As a leading Chinese nutraceutical powder exporter and contract manufacturer, we have mapped key technological and supply chain shifts that B2B brand owners, buyers, and chief science officers (CSOs) must navigate to retain competitive advantage:
Traditional botanical extraction faces seasonal supply variability, heavy metal contamination, and sustainability constraints. Precision fermentation—demonstrated in our 3-FL HMOs (99% HPLC)—utilizes bio-engineered micro-organisms to produce nature-identical human milk oligosaccharides and complex peptides with zero endotoxins, consistent yield, and 99%+ batch-to-batch chemical identity.
Hydrophobic bio-actives like DHA, Coenzyme Q10, and Curcumin suffer from poor physiological absorption. The industry standard is shifting toward spray-dried microencapsulation and liposomal encapsulation technology. Microencapsulation protects volatile fatty acids (e.g., 30% DHA Powder) from oxidation while turning oil-based actives into instant cold-water dispersible powders.
Regulatory bodies including the US FDA, European EFSA, and China NMPA have tightened heavy metal (Pb, As, Cd, Hg) limits to parts-per-billion (ppb) levels. Infant formulas, longevity NMN capsules, and cellular health powders require strict endotoxin screening (<0.05 EU/mg) to prevent systemic inflammatory responses in vulnerable populations.
Information gain relies on empirical proof. Our modern analytical testing facility utilizes High-Performance Liquid Chromatography (HPLC), Inductively Coupled Plasma Mass Spectrometry (ICP-MS), and Gas Chromatography-Mass Spectrometry (GC-MS) to validate every kilogram of material leaving our factory floor.
| Nutraceutical Active | Assay Method | Factory Purity Spec | Heavy Metals (Pb/As/Cd/Hg) | Microbiological Standard | Primary Industrial Application |
|---|---|---|---|---|---|
| Ginseng Adventitious Root Extract | HPLC / UV-Vis | Ginsenosides ≥ 80.0% | < 0.1 ppm Total | TPC < 1,000 CFU/g | Immunomodulation, Nootropics |
| 3-FL Human Milk Oligosaccharide | HPLC / HPAEC-PAD | 3-Fucosyllactose ≥ 99.0% | Heavy Metals < 0.05 ppm | Endotoxin < 0.005 EU/mg | Infant Formula, Microbiome Therapeutics |
| Coenzyme A (CoA) CAS 85-61-0 | Enzymatic / HPLC | Active CoA ≥ 95.0% | < 0.5 ppm Total | Pathogens Negative / 25g | Cellular Metabolism, Liposomes |
| Ellagic Acid (Punica granatum) | HPLC Standard | Ellagic Acid ≥ 98.0% | < 1.0 ppm Total | Molds/Yeast < 100 CFU/g | Anti-aging, Anti-glycation Supplements |
| Fish Collagen Tripeptides (CTP) | HPLC / Gel Filtration | Gly-Pro-Hyp ≥ 3.0% | < 0.05 ppm Total | TPC < 500 CFU/g | Nutricosmetics, Bone & Joint Health |
| Beta-NMN (Nicotinamide Mononucleotide) | HPLC / NMR | Beta-Anomer ≥ 99.5% | < 0.1 ppm Total | Total Aerobic < 100 CFU/g | NAD+ Synthesis, Longevity Formulations |
Building a resilient dietary supplement brand requires more than raw ingredient sourcing. It demands a vertically integrated manufacturing partner capable of scaling seamlessly from small pilot runs to high-throughput container-load shipments. Combining strict Western regulatory compliance (NSF/ANSI 455-2 cGMP, FDA-registered facilities) with China's ultra-efficient bio-manufacturing supply chain, we deliver unprecedented cost efficiency, purity, and turnaround speed.
Operating across 50,000+ square meters of Class 100,000 cleanroom capacity, our facility houses high-speed rotary tablet presses, automated capsule encapsulation lines handling 5.5 Million capsules per day, and industrial three-dimensional V-blenders for uniform powder homogenisation.
Eliminate multi-vendor friction. We provide turnkey private label solutions including primary bottle blowing (PET/HDPE/Glass), nitrogen-flush pouch filling, induction sealing, anti-tamper shrink wrapping, and in-house compliance review for Supplement Facts panels (FDA & EU aligned).
Every batch undergoes strict identity testing (FTIR / HPLC), heavy metal quantification (ICP-MS), solvent residue analysis (GC), and microbial load verification. Full batch records, Certificates of Analysis (CoA), SDS, and stability data are supplied with every order.
Molecular stability evaluation, flavor masking, active dose optimization, and ingredient sourcing.
Supplement Facts verification, allergen declaration, structure-function claim check, and artwork prep.
3D powder homogenization, fluid-bed granulation, microencapsulation, or precision fermentation batching.
Analytical COA issuance, stability retention sampling, container loading, and global door-to-port export shipping.
Clear answers to critical technical, regulatory, and logistics questions faced by procurement directors, brand owners, and supply chain managers when importing nutraceutical powders from China.
For standardized bulk raw material powders (e.g., NMN, Ellagic Acid, Ginseng Extract), our standard MOQ starts at 1 kg to 25 kg (drum size) for stock ingredients. For custom private label powder formulations (e.g., custom Supergreens or Collagen Blends), the MOQ typically starts at 1,000 units/tubs depending on container sizing and custom flavoring complexity.
Hygroscopic active ingredients like Coenzyme A, NMN, and Amino Acid powders are processed in climate-controlled cleanrooms maintaining relative humidity (RH) below 35%. Packaging includes pharmaceutical-grade double PE inner liners, aluminum foil vacuum shielding, and food-grade silica desiccants inside fiber drums or sealed canisters.
Every shipment is accompanied by a full export documentation pack, including: Batch Certificate of Analysis (COA) with HPLC/ICP-MS results, Material Safety Data Sheet (MSDS), Technical Data Sheet (TDS), Flowchart of Process, Allergen Statement, Non-GMO Declaration, Kosher/Halal Certificates, and Certificate of Origin (COO).
Yes. We offer custom micronization and particle size classification ranging from 80 mesh up to 300 mesh. We also engineer instantized powders (using lecithin or sunflower oil coating) to ensure rapid cold-water solubility without clump formation in ready-to-drink (RTD) beverage powders.
Our 3-FL HMO is produced via genetic precision fermentation using non-pathogenic E. coli K-12 derivative strains. Post-fermentation downstream processing involves multi-stage membrane filtration, ultrafiltration, ion exchange chromatography, and crystallization to strip endotoxins down to <0.005 EU/mg, exceeding international infant formula safety benchmarks.
In-stock raw material powders ship within 3 to 5 business days following QA release. Custom contract blending, flavoring, and private label bottling runs typically require 3 to 4 weeks, which includes raw material quarantine, pilot blending, labeling, packaging, and final analytical CoA clearance.
Absolutely. We welcome third-party facility audits from agencies such as SGS, Intertek, or Eurofins, as well as direct client quality assurance audits. Our quality management system maintains complete batch production records (BPR), calibration logs, cleaning validation records, and material traceability for up to 5 years.
We utilize high-pressure homogenization technology to encapsulate water-soluble or fat-soluble active ingredients inside phospholipid bilayers (sunflower or soy lecithin). This produces liposomal dry powders with lipid vesicle sizes between 100nm–200nm, protecting active ingredients from gastric acid degradation and boosting cellular absorption up to 5-fold.
Partner with China's leading nutraceutical powder factory and exporter. Access wholesale pricing, request free laboratory samples, or consult with our R&D formulation engineers.
