- About Us
We make the extract. We don't trade it.
We are a GMP-certified manufacturer of standardized botanical ingredients. Our factory, our laboratory — fully owned, fully controlled, fully accountable to you.
"Most quality problems in botanical ingredients start at the supplier. We decided the only way to fix that was to control everything — from the field to your freight forwarder."
- GMP Certified Facility
Manufacturing under current Good Manufacturing Practice certification
- ISO Quality Management
ISO 9001 certified quality management system across all production processes
- In-House QC Laboratory
Fully equipped on-site laboratory — every batch tested internally before release
- 200+ Botanical species
Extracts · Fluid Extracts · Granules · Compounds
"Most quality problems in botanical ingredients start at the supplier. We decided the only way to fix that was to control everything — from the field to your freight forwarder."
We built this because we kept seeing the same problems: inconsistent active content, missing documentation, contamination that cleared one port and failed the next. The only way to guarantee none of that happens is to be the manufacturer — and to stand behind every certificate of analysis we sign.
- Instrument Inventory
From a single extraction focus to an industry-leading global supply network
Was founded in 2021 in Sanmenxia, Henan Province — one of China’s most botanically rich regions. We began with a strategic focus on Forsythia and a 60-acre modern production base, but we were driven by a broader mission. We knew international buyers struggled with one fundamental problem: they couldn’t trust what was in the bag.
To solve this, our early years were defined by a relentless obsession with standardization. Before scaling up, we built our own in-house analytical laboratory. We treat every batch as if it were going to a pharmaceutical manufacturer — because, with our 39 national drug production approvals, it often is.
It starts with sourcing. Every raw material we purchase must meet two non-negotiable criteria: it comes from an authenticated geo-origin — what traditional Chinese medicine calls daodi — and it passes full testing against the Chinese Pharmacopoeia. If a batch doesn’t meet both, it doesn’t enter our facility.
By April 2023, we had earned our GMP certification. While many herbal extract suppliers find this level of process control too demanding, for us, it was the baseline, not the ceiling.
“We realized that the only way to earn the trust of European and American buyers wasn’t to talk about quality — it was to document it, batch by batch, in terms they could verify independently.”
Our commitment to verifiable quality fueled rapid global expansion. In 2024, our facility entered full-scale operation, marking our first successful international exports. By 2025, we were recognized as a National High-Tech Enterprise, established joint R&D centers with leading universities, and secured the exclusive geographical indication usage rights for “Lushi Forsythia.”
Today, our annual processing capacity exceeds 10,000 tons, ranking first in the north of the Yangtze River. We serve international clients across diverse regulated sectors, offering a catalog that spans over 200 botanical species.
We are still privately held. Headquartered at our modern production base. Still running our own GMP factory. Still the direct manufacturer.
- Our facility
23,000m² — built for international-grade production
Our GMP-certified production facility in Lushi County operates four dedicated production lines. Every area — from incoming raw material quarantine to finished goods warehouse — is controlled, documented, and open to client audit.
23,000
m²
GMP-certified production facility
5000 MT
/ year
Annual extraction capacity
9
Multi-Functional
Extraction Tanks
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- Factory
- Products
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Factory
Exhibition Hall - Honor
Team
Exhibition Hall — Patents
Exhibition Hall – Finished Products
Exhibition Hall — Traditional Chinese Medicinal Materials
Exhibition Hall — Granules
Exhibition Hall — Baicalin Extract
Exhibition Hall – Honeysuckle Extract
Exhibition Hall — Forsythia Extract
Exhibition Hall — Banqing Granules
Factory
Factory
Factory
Factory
Factory
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Herb Extract in the format your process actually needs
Each form is designed around a specific manufacturing workflow. Choose by your administration route, mixing equipment, and regulatory market.
01
Dry Powder Extract
Most concentrated form
Highly concentrated, spray-dried powder derived via water or ethanol extraction, with strictly standardized active markers. Offers excellent flowability and stability. Ideal for human dietary supplements (capsules/tablets) and serves as a premium feed additive base for livestock and aquaculture.
02
Fluid & Soft Extracts
Liquid concentrate
Premium liquid extracts optimized for rapid absorption and seamless formulation. Perfectly suited for cosmetic serums, personal care formulations, and high-purity oral liquid medications for both human and veterinary applications.
03
Soluble Granule
Instant dispersal
Engineered for complete and rapid water solubility without sedimentation. Perfect for human functional beverages and large-scale animal drinking water systems, ensuring zero clogging in automated farm dosing lines.
04
Custom Formulation
Targeted multi-industry solutions
Pre-blended synergistic formulas tailored to specific industry requirements. Whether formulating a complex nutraceutical or a specialized veterinary treatment, we customize active ratios to meet strict regional compliance and functional goals.
05
Raw Botanical Powder
Custom 60–500 mesh sizing
Premium botanical materials directly milled to precise particle sizes (60–500 mesh). This mechanical process retains the plant’s natural fiber and full-spectrum profile without extraction. A highly cost-effective solution ideal for human dietary capsules, herbal tea blends, and bulk animal feed premixes.
- Raw material sourcing
We apply two binding criteria before a single kilogram enters our facility.
The quality of a botanical extract is determined almost entirely by the quality of the raw material that goes into it. Most suppliers in China buy on the commodity spot market — whoever offers the cheapest price on the day. We don’t.
Most ingredient failures begin before extraction — not in the lab, but at the farm gate. Our procurement process enforces two independent standards that must be satisfied simultaneously. Neither alone is sufficient.
01
Only geo-authenticated botanical material from recognized Dao-Di origins accepted
“Dao-Di” is the Chinese pharmacological designation for geo-authentic medicinal plants — botanical material whose active compound concentration is directly tied to the specific geography, altitude, climate, and soil conditions of its origin. This concept has been documented in classical materia medica for over 1,500 years and is formally recognized in the Chinese Pharmacopoeia (CP 2020) as a quality-determining criterion.
The same medicinal plant species from different origins can vary in active compound concentration by 30–50% or more. For each botanical material we source, we lock in its nationally recognized Dao-Di origin and accept no “equivalent” substitutes, regardless of price advantage.
Verified Botanical Source
Each raw material must match the declared botanical species, plant part, and origin information. Supplier declarations are reviewed together with incoming inspection records to reduce the risk of substitution, adulteration, or mixed-origin material.
Documented Origin Per Incoming Lot
Every incoming lot is accompanied by supplier documentation, including origin information, harvest or collection records where applicable, and batch traceability documents. These records are archived and can be provided to customers upon request.
Harvest And Post-Harvest Control
Harvest season, plant maturity, drying method, storage condition, and transportation process are reviewed as part of incoming material evaluation. Materials showing signs of mildew, improper drying, abnormal odor, visible contamination, or poor storage are rejected.
Approved Supplier And Producing Area
We work with qualified suppliers and stable producing areas to reduce raw material variability. Supplier performance is evaluated continuously based on origin consistency, documentation reliability, incoming test results, and long-term batch stability.
02
Chinese Pharmacopoeia (CP 2020) · Every parameter, every batch
The Chinese Pharmacopoeia (CP 2020) establishes legally binding quality standards for all listed medicinal materials, specifying minimum active compound content, heavy metal limits, pesticide residue thresholds, and authentication requirements by thin-layer chromatography.
We treat the pharmacopoeia standard as the floor, not the ceiling: our internal incoming material specifications for key markers are set above the pharmacopoeia minimum to provide a buffer against batch-to-batch variability. Any batch meeting origin requirements but failing any pharmacopoeia parameter is rejected without exception. There is no commercial override for out-of-specification incoming material.
TLC species authentication — every incoming lot
Thin-layer chromatography fingerprint comparison against CP 2020 reference standard. Confirms botanical identity and rules out adulteration with related Forsythia species or unrelated substitutes before acceptance.
Rigorous Macroscopic Sorting & Cleaning
Before processing, all raw herbs undergo comprehensive visual inspections. We strictly screen for and remove foreign matter, substandard pieces, and soil residues, ensuring only premium-grade materials enter our warehouse.
Active Marker Or Assay Testing
Key active markers or characteristic compounds are tested by HPLC, UV, TLC, or other validated methods depending on the botanical material and product specification. Internal acceptance limits are set to support stable extract potency and consistent finished-product performance.
Physical Condition & Milling Readiness
Before any material is cleared for custom milling, we evaluate its physical condition, drying state, and structural integrity. This ensures the raw herb is perfectly conditioned to achieve your exact mesh specifications and optimal flowability.
PRE-PURCHASE ACTIVE COMPOUND TESTING · APPLIED BEFORE ANY LOT IS ACCEPTED
We test active compound content in the raw herb before procurement — not after.
The most common source of batch-to-batch inconsistency in botanical extracts is variability in raw material active compound density — which is invisible from the outside and undetectable by visual inspection alone. We address this at the point of origin: before any lot is commercially committed, a representative sample is submitted to our QC laboratory for HPLC quantification of the primary and secondary active markers in the raw, unprocessed herb. Lots falling below our internal incoming material specification — set above the CP 2020 minimum — are rejected regardless of commercial pressure or supply availability. This pre-purchase testing step is what allows us to guarantee a finished extract specification rather than merely target it.
- R&D Team
The people behind the specification
We’re not a trading company. When you have a formulation question or a quality issue, you’re talking to the person who was in the lab. Every technical claim we make is backed by someone with direct production accountability.
A note on technical support: Our team handles formulation questions, dosage guidance, regulatory documentation, and compatibility questions as part of the standard buyer relationship — not as a paid consulting service. If you have a technical question before ordering, ask us.
Prof. Dr. Zhao Jinzhong
Chief Scientific Advisor
Over 20 years of expertise in medicinal chemistry and chemical biology. Lead researcher specializing in the discovery, extraction, and functional application of bioactive plant compounds. Has authored over 70 high-impact papers in leading international journals and holds multiple patents for natural product extraction technologies.
Prof. Dr. Zhang Yongpo
Senior R&D Scientist
Specializes in organic chemistry and the targeted extraction of natural active ingredients. Leads formulation methodology and coordination chemistry research to enhance the stability and bioavailability of botanical extracts. Published extensively in leading molecular structure and inorganic chemistry journals.
Dr. Yin Congcong
Lead Analytical Scientist
Senior experimentalist bridging raw material analysis with biochemical applications. Directs advanced laboratory testing protocols and biological activity evaluations to ensure absolute batch-to-batch consistency and active compound standardization.
Dr. Guo Dongdong
Extraction Process Engineer
Expert in green chemistry and advanced organic synthesis. Focuses on scaling up laboratory extraction parameters into highly efficient, sustainable industrial production lines, optimizing solvent routes and temperature controls to maximize active ingredient yields.
- What we stand for
Not principles. Policies.
We don’t display values on a wall. We translate them into operational policies that affect every shipment we make.
01
Spec-locked, not spec-estimated
We guarantee active constituent content within ±5% of the stated specification on every TDS. If a batch falls outside this range, it doesn’t ship — it gets reprocessed or scrapped. There is no “close enough” in our CoA issuance policy.
"Active content is not a target. It is a commitment."
02
Documentation before excuses
Every order ships with a complete documentation package: CoA, MSDS, TDS, origin certificate, phytosanitary certificate, heavy metal and pesticide reports. This is not an add-on. It is our minimum standard — because without documentation, your product cannot clear customs and cannot be registered in your market.
"If your customs agent needs it, we provide it. As standard."
03
Problems owned, not passed
When there is a quality dispute, our QA manager is the first call — not your account manager. We investigate, we report the root cause in writing, and we resolve it. Third-party re-testing is supported. We retain batch samples for 24 months. Responsibility is not something we route around.
"Your QA problem becomes our QA problem. That's how partnerships work."
- Quality System
Every batch tested. Every test published.
Our QC process reflects the dual-marker standard — both APS polysaccharides and Astragaloside IV on every production lot, not just on registration batches.
Incoming raw herb verification
Origin authentication, active compound assay (HPLC), and TLC species confirmation before raw material enters production.
In-process and final product testing
Moisture, active compound assay (HPLC/UV), mesh size, microbiology. Final product CoA issued only after all parameters pass QA sign-off.
24-month retained sample program
Every production batch retained under controlled conditions for 24 months. Independent third-party retesting (SGS, Intertek, Bureau Veritas) accepted as binding on both sides.
Cross-functional issue resolution
Quality claims routed through your sales manager instantly trigger a joint QA and production task force. Formal root-cause analysis within 5 business days. Resolution confirmed in writing before action taken.
GMP Certified
Veterinary extract facility
ISO 9001
Quality management system
Chinese Pharmacopoeia
CP 2020 full compliance
Export Certified
All over the world markets
"We publish the measured value, not just the minimum."
If APS tests at 73.4%, our CoA says 73.4% — not “≥70%”. That’s the difference between a document that proves quality and one that merely asserts it.
- Sample CoA — Forsythia Extract (Phillyrin >6%)
- Manufacturing Flow Chart (Standard Botanical Extraction)
- Heavy Metal & Pesticide Residue Panel
- GMP Facility Certificate
- Raw Herb Origin & Traceability Statement
- Stability Study Summary (24-month)
- Long-term commitment
Rapid Growth with Strong Investment — Building for the Future
One of the legitimate concerns international buyers have about Chinese suppliers is longevity. It’s a fair question. The ingredient market has seen suppliers appear, grow quickly, cut corners, and disappear — leaving their clients scrambling for alternatives.
We have been operating under the same ownership, the same management team, and the same commitment to manufacturing standards since startup. We are not VC-funded. We are not chasing rapid growth. We are building a supply relationship that outlasts the first shipment.
"We have clients who placed their first order with us and are still ordering today. That is the only metric that matters to us."
We invest in infrastructure — facility expansion, certification, R&D capability — because we are planning for the next decade, not the next quarter. When you qualify us as a supplier, you are investing time and resources. We take that seriously.
Privately held, founder-led
No external investors requiring quarterly growth targets. Decisions are made with long-term client relationships in mind, not short-term margin optimization.
Pricing transparency
We explain what drives cost changes when raw material prices shift. We don't absorb losses silently and compensate with quality cuts. We tell you.
Annual supply planning
For clients with predictable volumes, we offer annual supply agreements with confirmed allocation, locked pricing, and priority production scheduling.
Continuous product development
Our R&D team actively develops new extract specifications and compound formula solutions. Client-requested new products are the first priority in our R&D pipeline.
No minimum on first sample
We want you to verify our product before committing. Request a free sample with no minimum quantity, no commitment.
Ready to verify us for yourself?
Request a sample, arrange a factory audit, or speak directly with our technical team. We don’t use scripts. You’ll speak to someone who actually knows the product.