Honeysuckle Extract

Lonicera japonica Thunb. · Chlorogenic Acid ≥3% HPLC · CP 2020

“Ethically sourced from globally recognized optimal terroirs. We provide HPLC quantification on every batch, ensuring exceptional stability and purity. Delivering premium botanical solutions engineered for the global pharmaceutical, nutraceutical, personal care, and food & beverage industries.”

100% Pure Extracts: Carrier-Assisted Only When Scientifically Required.

≥3%

Chlorogenic acid · HPLC

Premium Terroir

Henan & Shandong origin

CP 2020

Chinese Pharmacopoeia std.

4 Grades

Pharma · Health · Vet · Cosm

Honeysuckle Extract

Lonicera japonica Thunb. · Henan / Shandong Dao-Di

Raw Honeysuckle Powder

Honeysuckle Extract 10:1 20:1 or More

Chlorogenic Acid ≧ 5% （HPLC）

Chlorogenic Acid ≧ 4% （HPLC）

Chlorogenic Acid ≧ 3% （HPLC）

Industry-Specific Customization
Tailored active compound ratios (e.g., Chlorogenic Acid up to 10%+) and custom solubility profiles to meet your exact formulation and compliance requirements across all sectors.

GMP

Certified facility · Lushi

CoA

Issued for every batch

24 Mo

Retained batch samples · Stability data

CP 2020

Chinese Pharmacopoeia

R&D Team

PhD-led formulation support

What honeysuckle extract buyers typically run into

Honeysuckle (Lonicera japonica) is a premium botanical, but rampant adulteration makes cross-industry sourcing difficult. Whether formulating for human pharmaceuticals, veterinary health, dietary supplements, or cosmetics, buyers face synthetic spiking and mislabelled grades. Here is how our extraction facility addresses each specific industry problem.

Inconsistent quality from middleman brokers

Most suppliers are trading companies without manufacturing capabilities. This leads to hidden markups, unstable supply chains, and zero control over the actual extraction process.

Delayed or skipped QC testing

Many suppliers rely entirely on third-party labs. Because external testing is expensive and slow, they often test only selectively, allowing out-of-spec batches to slip through unseen.

Zero traceability for post-delivery issues

If a formulation fails stability testing months after purchase, ordinary suppliers have no reference material to trace the root cause, leaving buyers to absorb the loss.

Rigid specs causing regional import holds

Different regions (EU vs. US) have drastically different pesticide and heavy metal thresholds. Generic "one-size-fits-all" extracts frequently fail border compliance inspections.

Synthetic spiking passes basic tests

Rampant market adulteration means synthetic Chlorogenic Acid (CGA) is often spiked into low-grade extracts to pass simple, single-marker HPLC tests.

Depletion of volatile compounds to save energy

To minimize overhead, many mass-market suppliers bypass the energy-intensive condensation phase during extraction. This allows crucial heat-sensitive volatile oils to evaporate and be permanently lost, resulting in an incomplete, lower-efficacy extract.

Direct Manufacturer Quality Control

We own the extraction facility in Lushi. From raw material intake to the final extract, we maintain end-to-end control, ensuring identical quality and consistent supply across every batch.

Real-time In-House Laboratory

Our facility operates a dedicated, on-site QC department. We perform real-time testing during the production run, catching and correcting deviations immediately, rather than waiting for post-production surprises.

24-Month Retained Sample Library

We retain physical samples of every dispatched batch for 24 months. This guarantees absolute traceability, supports your long-term stability studies, and provides concrete evidence for any technical troubleshooting.

Customized Testing & Compliance

We don't offer generic promises. Instead, we customize our pesticide and heavy metal screening protocols (via certified third-party partners) tailored exactly to your specific regional regulations and formulation requirements.

Strict Pharmacopoeia (CP) Testing Standards

We strictly test every batch according to the rigorous standards of the Chinese Pharmacopoeia (CP). This pharma-level analytical methodology ensures authentic botanical identity and definitively exposes any synthetic spiking.

Full-Spectrum Retention via Active Condensation

We mandate continuous condenser operation during the extraction process to meticulously capture and retain all valuable volatile oils. We willingly absorb this steep operational premium — an extra 100 RMB per hour in electricity alone — to guarantee a fully potent, uncompromised final product.

Honeysuckle Extract — from pharmaceutical formulations to everyday wellness

Four standardized concentration grades cover every downstream application. Each grade is purpose-built for its sector, with a separate production specification, cleaning validation, and CoA template.

01 Drug Manufacturing

Honeysuckle extract is a foundational ingredient in China’s most widely prescribed OTC and ethical drug formulas for upper respiratory tract infections, fever, and viral conditions.

Classic botanical API for OTC cold, flu, and fever formulations
Active ingredient for natural antiviral and respiratory tract liquids/syrups
Compound Honeysuckle Granules for respiratory infections
API intermediate for chlorogenic acid enrichment formulas
CP 2020 compliant · Full pharma dossier on request

02 Nutraceuticals & Functional Foods

Immune support, antioxidant, and anti-inflammatory positioning are driving global demand for honeysuckle extract in dietary supplement formats, functional beverages, and wellness products.

Immune support capsules and tablets — seasonal cold & flu category
Throat lozenges and throat spray formulas
Antioxidant blend supplements (paired with green tea / astragalus)
Functional beverage and ready-to-drink immune support formats
Novel food or GRAS status documentation support available

03 Skincare & Personal Care

Honeysuckle extract is one of the most widely used botanical actives in functional skincare, delivering clinically supported anti-acne, antioxidant, and anti-inflammatory benefits alongside appealing natural brand positioning.

Anti-acne serums and spot treatments — antibacterial against C. acnes
Antioxidant face creams and vitamin C synergy formulas
Soothing and anti-redness formulations for sensitive skin
Natural preservative booster (chlorogenic acid antimicrobial activity)
EU Cosmetics Regulation compliant · INCI listed · low solvent grade

04 Animal Health & Feed Additives

As antibiotic growth promoter restrictions tighten globally, honeysuckle extract is one of the most well-documented botanical alternatives for respiratory health and immune support in production animals.

Poultry respiratory health — Supporting respiratory integrity during seasonal or environmental challenges
Swine immune health — Advanced botanical immune modulation for herd wellness
Aquaculture bacterial infection prevention (drinking water / feed additive)
Ruminant (cattle, sheep) anti-inflammatory and antipyretic applications
Water-soluble granule form ideal for drinking water delivery in flocks

Honeysuckle 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.

Chinese Pharmacopoeia compliance by application

Tailored extraction parameters and quality controls to meet the exact regulatory and formulation requirements of your sector.

Why strict Pharmacopoeia (CP) testing matters: Simple tests can be easily fooled by market adulteration. We protect your brand by strictly testing every batch against the rigorous analytical standards of the Chinese Pharmacopoeia (CP). This pharma-level methodology ensures authentic botanical identity, consistent potency, and zero compromise on quality.

Grade	TARGET APPLICATION	CHLOROGENIC ACID	KEY SPECIFICATIONS	IDEAL FORMAT
Pharmaceutical Grade	OTC formulas, APIs, Syrups	≥ 25% – 50% (HPLC)	Strict CP 2020 compliance; Ultra-low heavy metals & microbiology limits	Dry Powder / Liquid
Nutraceutical & F&B Grade	Dietary supplements, Functional beverages, Gummies	≥ 5% – 25% (HPLC)	100% water-soluble; No sedimentation; Mild flavor profile	Soluble Granule / Liquid
Cosmetic & Personal Care Grade	Serums, Anti-acne creams, Lotions	≥ 5% – 10% (HPLC)	Low solvent residue; Lighter color profile to prevent formulation staining; INCI compliant	Dry Powder / Fluid Extract
Veterinary & Animal Nutrition Grade	Feed premix, Drinking water programs, ingection Grade	≥ 3% – 5% (HPLC)	Cost-effective standardized marker; High heat stability for pelleting	Soluble Granule / Powder

Water or alcohol extraction— customized to your specifications. Centrifugal spray drying

Why the extraction solvent matters: Water extraction perfectly preserves hydrophilic active compounds, making it the ideal choice for end products requiring strict clean-label compliance. Conversely, ethanol extraction provides superior selectivity for higher-purity targets, significantly increasing the yield of core active ingredients while minimizing inactive impurities. We dynamically tailor the solvent route based on your specific application and regulatory market.

Both extraction routes feed into our advanced centrifugal spray drying system, which utilizes strict low-temperature controls to protect heat-sensitive active ingredients. From raw botanical material to finished free-flowing powder, we proudly maintain an active compound loss rate of < 3%.

Tailored to your application

Pure Water Extraction

Using purified water as the solvent, multiple cycle extractions are performed on the botanical raw materials under controlled temperature and time conditions. The water extraction method can fully dissolve hydrophilic active ingredients, such as water-soluble flavonoids and polysaccharides. The resulting product features excellent water solubility and is ideal for health supplements, cosmetics, and veterinary applications that require “no organic solvent residues,” perfectly aligning with “clean label” standards in the EU and US.

Extraction Solvent

Purified Water

Extraction Temperature

80–95°C

Extraction Time

1.5– 2 hrs × 2-3 times

Solid-Liquid Ratio

1:10–15 (w/v)

Solvent Residue

Not Applicable

Applicable Certification

EU / US Clean Label

No organic solvent residues — no ICH Q3C solvent residue testing required, reducing compliance costs.
The recovery rate of water-soluble active compounds is up to 20–30% higher compared to ethanol extraction, ensuring superior cold-water solubility of the finished product.
Suitable for clean label health supplements and cosmetic raw materials — meets EU EC No 1223/2009 requirements.
For functional beverages and animal nutrition, it dissolves rapidly in cold water without the need for additional solubilization treatments.

Ethanol Extraction

Using ethanol (typically 60–75% concentration) as the solvent, lipophilic (fat-soluble) active ingredients and specific aglycones are selectively enriched by adjusting the solvent polarity. Compared to water extraction, ethanol extraction can increase the yield of target active ingredients by 30–40%, while significantly reducing the co-extraction of hydrophilic inactive impurities (such as polysaccharides and mucilage), thereby streamlining subsequent purification steps. It is highly suitable for producing high-concentration botanical extracts and pharmaceutical-grade export products.

Extraction Solvent

60–75% Ethanol

Extraction Temperature

50–65°C

Extraction Time

1.5–2 hrs × 2-3 times

Solid-Liquid Ratio

1:10–12 (w/v)

Solvent Recovery

Closed reflux ≥ 90%

Residue Standard

ICH Q3C Class 3

The extraction rate of specific target active ingredients is increased by 30–40% — enabling the production of higher concentration specifications with the same raw material input.
Co-extraction of inactive polysaccharides is reduced by about 40%, leading to higher efficiency in subsequent concentration and purification, resulting in better finished product purity.
Closed reflux extraction ensures the loss of volatile active ingredients is < 5%, and the ethanol recovery rate is ≥ 90%.
All batches are tested for residual ethanol according to the ICH Q3C standard, meeting pharmacopeia requirements, and a CoA is provided with shipments.

Centrifugal Spray Drying

The concentrated water or ethanol extract enters the centrifugal spray drying tower, where a high-speed rotating atomizer disc disperses the liquid into uniform, fine droplets. This significantly increases the gas-liquid contact area, completing moisture evaporation in an extremely short residence time. The powder is dried and shaped before reaching the tower wall. The inlet air temperature is precisely controlled throughout the process, and the actual temperature of the material during drying does not exceed 55°C — ensuring that heat-sensitive active ingredients are completely preserved during the powdering process.

Atomization Method

Rotary atomization

Inlet air temperature

160–180°C

Actual material temperature

≤ 55°C

Powder moisture content

≤ 5%

Particle size range

20–80 μm

Activity retention rate

≥ 97%

High-speed rotating atomization by the centrifugal disc produces uniform droplet sizes. After drying, the powder exhibits excellent flowability and consistent bulk density.
The actual material temperature remains ≤ 55°C throughout the process, and the thermal degradation rate of active ingredients is < 3%, which is significantly lower than traditional spray drying methods.
The porous, low-density powder structure dissolves quickly in cold water without clumping, facilitating direct use in end formulations.
The same system is compatible with both water and ethanol extracts. Both extraction routes can be seamlessly connected without the need to switch drying equipment.

Key Process Parameters

Actual Material Temperature

≤ 55 °C · Fully Monitored

Active Retention Rate

≥ 97 % · HPLC Verified

Finished Product Moisture Content

≤ 5 % · Drying Method

Particle Size Range

20–80 μm · Laser Particle Size

Compared to traditional spray drying: Traditional spray drying involves an inlet temperature exceeding 160°C, meaning materials are exposed to high temperatures for extended periods. The thermal degradation rate of heat-sensitive active components can reach 5–15%. Centrifugal spray drying drastically shortens droplet residence time via high-speed atomization. The actual temperature of the material never exceeds 55°C, keeping active loss < 3%. Liquids from both extraction routes can be fed directly into this system without needing equipment reconfiguration.

Compatible with Both Extraction Routes

The condenser valve stays open — for every hour, every batch.

Why this matters: During hot extraction, volatile oils — the terpene- and phenylpropanoid-based compounds responsible for much of a herb’s biological activity — vaporize with the solvent steam. In an open system with no condenser running, that steam vents to atmosphere, carrying the volatile fraction with it. The extract you end up with may pass an HPLC marker spec and still be missing 40–70% of its original volatile oil content. Running the reflux condenser throughout captures that steam, condenses it back to liquid, and returns it to the extraction vessel. Nothing leaves.

We operate our reflux condenser — with cooling water flowing and the condenser valve fully open — for the entire duration of every extraction run. Minimum run time is four hours. It costs more in electricity. We consider it non-negotiable.

Extraction without active reflux

Cooling water bypassed or switched off · Open-vent system

When the condenser valve is closed or the cooling water is off, the condenser becomes non-functional. Steam rising from the boiling extraction passes straight through and vents via the exhaust port. Monoterpenes, sesquiterpenes, and volatile phenylpropanoids — which are carried efficiently by steam even at temperatures well below their individual boiling points — are lost to the atmosphere continuously throughout the run.

Solvent heats; volatile oils vaporize and rise with steam toward condenser

Condenser inactive — no cooling; steam passes straight through without condensing

Steam vents through exhaust port; volatile oils exit with it — gone for good

This repeats every minute of the extraction run — losses accumulate over the full 4+ hours

40–70%

Typical volatile oil loss in an open-vent system

Varies by herb species, boiling point of target compounds, and run duration. Higher for monoterpene-rich herbs (mint, perilla, cyperus); somewhat lower for sesquiterpene-dominant herbs due to higher molecular weight.

Volatile oil fraction arrives in the finished extract at 30–60% of its original concentration in the raw herb
Marker compounds (e.g. essential oil HPLC value) may still "pass" specification — the spec was set too low or doesn't cover the full volatile profile
Losses are irreversible — cannot be corrected at the drying or blending stage
Saves electricity; common in commodity-grade production where per-batch energy cost is a primary driver

Full reflux throughout the run

Cooling water flowing · Reflux condenser fully active · All 4+ hours

With the condenser valve open and cooling water circulating, the condenser maintains a temperature differential that causes rising steam to condense back to liquid on contact with the cooling surface. The condensate — solvent plus dissolved volatile oils — drips back into the extraction vessel. This cycle repeats continuously: vaporize, rise, condense, return. No volatile fraction escapes the system.

Solvent heats; volatile oils vaporize and rise with steam toward condenser

Condenser inactive — no cooling; steam passes straight Condenser active — cooling water flowing; steam contacts cold surface and condenses immediately without condensing

Condensate (solvent + volatile oils) drips back into extraction vessel — nothing lost

Cycle repeats continuously for the full run duration — volatile oil concentration in extract builds and holds

< 8%

Volatile oil loss with active reflux condenser

Residual losses attributable to minor condenser efficiency gaps and unavoidable head-space exchange during loading/unloading. The condenser itself retains >92% of the volatile fraction throughout the extraction cycle.

Volatile oil fraction is preserved in the extract at ≥92% of original concentration in raw herb
The full terpene and phenylpropanoid profile is carried through to the finished powder — not just the non-volatile markers
Consistent batch to batch: reflux conditions are stable and logged; volatile oil retention does not drift with operator decisions
Higher energy cost per batch is a deliberate process commitment, not an oversight

How the condenser is run

Parameters held for the full duration of every extraction batch

Condenser Valve

Fully open

Cooling Water

Continuous flow

Coolant Inlet Temp.

15–20°C

Condensation Zone

Shell-and-tube condenser

Condenser Active From

Pre-heat to drain

Volatile Oil Retention

≥ 92%

Exhaust Port

Closed during run

Run Duration (min.)

4 hrs (≥ 240 min)

Why pre-heat to drain? Volatile oil loss begins the moment the solvent starts warming — even before boiling. We open the condenser valve at the start of the pre-heat phase and keep it open through the full drain cycle. Any batch record showing condenser activation only after the target temperature is reached has already allowed early-phase losses.

What running it correctly costs

Per-batch energy consumption — extraction stage only

Electricity rate 100 kWh / hour

Extraction vessel + heating elements + cooling water pump

100 kWh / hour

Minimum run time 4+ hours / batch

Full reflux from pre-heat through drain — per batch

4+ hours / batch

For any herb where volatile compounds contribute meaningfully to the target bioactivity — or where the volatile fraction is part of the product’s organoleptic identity (flavour, aroma, or functional fragrance in cosmetic use) — open-vent extraction without active reflux produces a fundamentally different product. The marker compound on the CoA may look identical. The volatile oil profile will not.

Process aids for stability. Not cheap fillers for profit.

In botanical extraction, maltodextrin is often a necessary carrier during spray drying to prevent sticky resins from caking and to ensure powder flowability. We use it strictly as a functional manufacturing aid—never as a post-production filler. We guarantee 100% transparency on carrier ratios, and we never dry-blend maltodextrin into finished batches just to lower costs. Need a 100% pure extract? We also offer custom carrier-free processing tailored to your specific botanical requirements.

“There is a massive difference between using a 5% carrier during spray drying to ensure powder stability, and dry-blending 40% cheap carbohydrate into a finished drum to slash prices. One is formulation science; the other is specification inflation. We only practice the former.”

Dry-blending

The liquid botanical extract is blended with a high proportion of maltodextrin (a cheap, tasteless carbohydrate derived from starch) before spray drying. Maltodextrin acts as a “carrier” that improves flowability and reduces dust — but it permanently dilutes the active compound concentration in the final powder.

Maltodextrin is added after drying solely as a cheap, inactive filler.
Carrier ratios are purposely hidden, making your formulation dosing highly inaccurate.
High risk of inconsistent active levels from scoop to scoop due to uneven mechanical mixing.
You ultimately pay botanical extract prices for carbohydrate starch.

Transparent carriers & custom pure options

When we use maltodextrin, it is wet-blended before spray drying strictly to encapsulate botanical actives and improve flowability.

Zero Dry-Blending: We never cut finished powders with fillers to artificially lower our manufacturing costs.
Locked-in Consistency: When a processing aid is required for physical stability, its precise ratio is strictly locked into our master manufacturing record to guarantee absolute batch-to-batch consistency.
Carrier is utilized only when the specific botanical resin demands it for moisture resistance and cold-water solubility.
Custom Carrier-Free Extracts: For specialized formulations, we can adjust our extraction parameters to deliver 100% pure, carrier-free extracts upon request.

0%

Dry-Blended Fillers

No maltodextrin is ever mechanically mixed into finished powders to cheat on weight.

100%

Carrier Transparency

Exact excipient ratios are explicitly stated on your CoA for precise formulation dosing.

Custom

Carrier-Free Options

Depending on the species, 100% pure botanical extracts are available upon request.

Verified

Active Markers

Honest active compound reporting guarantees your final product’s therapeutic efficacy.

We apply two binding criteria before a single kilogram enters our facility.

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 Geo-Authentic Origin And Qualified Supply Base

For botanical extracts, raw material quality is directly influenced by species identity, growing region, harvest season, climate, soil conditions, and post-harvest handling. We source raw materials from qualified producing regions and approved supply bases, with preference given to recognized geo-authentic origins where applicable.

Each incoming lot must be traceable to its declared botanical source, producing area, supplier, and harvest period. Mixed-origin, unclear-origin, or undocumented materials are not accepted for production, even when they appear to meet basic commercial specifications.

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 lot.

Origin alone is not sufficient. Each incoming raw material lot must pass identity, safety, and quality testing before it can be released for extraction or further processing. Our incoming inspection system is designed to confirm botanical authenticity, control contaminants, and maintain stable active-marker levels across production batches.

Testing requirements are established according to applicable pharmacopoeia standards, customer specifications, export market requirements, and internal quality limits. Any lot that fails an incoming inspection item is rejected or isolated for further investigation. There is no commercial override for out-of-specification raw materials.

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 target active compounds 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 quantitative analysis (e.g., HPLC/UV) of key 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.

Lushi — from raw material to export-grade extract, all under one roof.

Our facility is strategically located at the botanical source, featuring a fully integrated processing chain that covers raw material intake, primary processing, deep extraction, and final QC release. By controlling every step from raw biomass to finished powder, we eliminate middleman risks and guarantee consistent, export-grade extracts across all industry sectors. We are your reliable, vertically integrated manufacturing partner.

23,000m²

GMP-certified production facility

9

Extraction Vessels

5000+MT

Annual extract capacity

GMP

Certified facility
Third-party audits welcomed

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PRODUCTION FLOW — FROM RAW MATERIAL TO EXPORT-GRADE EXTRACT

01

Raw Material Intake & QC

Strict botanical verification

02

Water or Ethanol Extraction

Customized solvent route

03

Vacuum Concentration

Low-temp evaporation

04

Spray Drying

Excellent flow & solubility

05

Comprehensive QC Testing

CoA issued

06

Packing & Dispatch

Global express

Every document you need — prepared before you ask

Each certification was pursued because it solves a specific market access or buyer qualification requirement — not as a marketing exercise. We include scope, issuing body, validity period, and the market it is relevant to for every certificate.

Need originals for your supplier approval?

We dispatch full-resolution certificate scans, notarized copies, and issuing body contact details within 24 hours of request. No registration required.

ISO 2200:2018

An internationally recognized standard for food safety management systems. This certification demonstrates our rigorous approach to identifying and controlling food safety hazards throughout the entire plant extraction process. It assures our global B2B clients in the feed additive and human health sectors that our materials meet the highest safety protocols from sourcing to final delivery.

HACCP

A globally recognized systematic and preventive approach to managing biological, chemical, and physical hazards in production. By strictly monitoring critical control points during botanical extraction, we eliminate contamination risks at the source. This rigorous risk management framework is essential for clients requiring absolute purity and uncompromised safety.

Food Production License

The mandatory official authorization issued by national market regulation authorities, legally permitting the production of food and dietary supplement ingredients. It signifies that our manufacturing facilities, sanitation protocols, and QC systems have passed stringent government inspections, ensuring our extracts are fully compliant for human health and high-end feed applications.

GMP Certification

Pharmaceuticalgrade manufacturing standards applied to ourbotanical extraction operations. Significantly higher than standardfood-grade requirements -required by pharmaceutical clientsand veterinary drug manufacturers using our ingredients asstarting materials. Covers process validation,equipmentcalibration,environmental monitoring, and personnel training.

Veterinary Drug Production License

Covers the entire process of veterinary drug production, testing, storage, and release. Strictly audited and issued by the national agricultural administration, proving full compliance with Veterinary GMP standards. This is the mandatory legal prerequisite for manufacturing and distributing veterinary pharmaceutical products, ensuring all batches are safe, effective, and quality-controlled.

Business License

The fundamental legal document authorizing our corporate operations, issued by the State Administration for Market Regulation (SAMR). Verifies our registered capital, approved business scope, and legal representative. It serves as the legal foundation demonstrating full corporate legitimacy for all domestic and international commercial engagements.

ISO 9001 : 2015

Covers all production, testing, documentation, storage, and export processes. Audited annually by an accredited third-party certification body. Zero non-conformances in the last three consecutive audit cycles. The foundation standard required by most enterprise supplier qualification programs globally.

ISO 14001 : 2015

Internationally recognized standard for environmental management. Validates our commitment to minimizing our environmental footprint, reducing waste, and ensuring sustainable manufacturing practices. Covers wastewater treatment, emission controls, and resource efficiency. Essential for partnering with environmentally conscious global enterprises.

ISO 45001 : 2018

A comprehensive framework ensuring a safe and healthy workplace for all employees. Proactively prevents work-related injury and ill health through rigorous risk assessment and safety protocols. Covers hazard identification, emergency response mechanisms, and continuous safety training across all production facilities.

Open PDF file

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.

Every batch tested. Every test published.

Our QC process reflects a rigorous pharmacopoeia standard — quantifying target active markers on every production lot, not just on registration batches.

Incoming raw herb verification

Origin authentication, heavy metals (AAS), and TLC species confirmation before raw material enters production.

In-process and final product testing

Moisture, target active compounds (HPLC / UV-Vis), 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.

QA-direct issue resolution

All quality claims handled by QA Manager Zhang Lei — not routed through sales. Formal root-cause analysis within 5 business days. Resolution confirmed in writing before action taken.

GMP Certified

Extract facility

ISO 9001

Quality management system

Chinese Pharmacopoeia

CP 2020 full compliance

Export Certified

EU · US · SEA markets

"We publish the measured value, not just the minimum."

If the active marker tests at 26.4%, our CoA says 26.4% — not “≥ 25%”. That’s the difference between a document that proves quality and one that merely asserts it.

From our factory to your production line

Standard lead times, packaging options, and MOQ structure — so there are no surprises before your first order.

Sample Order

20-100g Free Samples

Full CoA, spec sheet, and pricing indication included with every sample. Shipped globally within 48 hours of request.

Quantity 20-100g
Packaging Sealed foil pouch
Shipping Express · SF/DHL / FedEx
Lead time 48 hours from request
Cost Sample Free

Trial Order

50 kg — formulation validation

Designed for formulation teams validating before committing to production volume. Available in all four application grades. Separate lot and dedicated CoA issued.

MOQ 50 kg per grade
Packaging 25kg drum (HDPE, UN-rated) or kraft bag
Shipping DAP / CIF · Buyer's preference
Lead time 7–10 business days
Documentation Full CoA + spec sheet

Production Order

1000 kg+ — standard commercial terms

Standard production orders available in 25 kg drums or 25 kg aluminum-lined kraft bags. Bulk pallet shipments on standard commercial trade terms.

MOQ 1000 kg per grade
Packaging 25kg drum (HDPE, UN-rated) or kraft bag
Shipping FOB / CIF destination
Lead time 15–20 business days (in-stock: 7 days)
Documentation Full CoA & Packing List

Shelf Life

24 months

Sealed, below 25°C, away from light and moisture

In-Stock Grades

All 4 grades

Pharma · Nutraceutical · Cosmetic · Veterinary

Payment Terms

T/T 100%

Against B/L or CoA — negotiable for regular buyers

Private Label

Available

Custom packaging, label, spec format from 25 kg order

Questions buyers ask before placing a first order

Our technical team answers these most frequently. If yours isn’t here, ask us directly — technical consultation is a standard part of our buyer relationship, not a paid service.

Q1: Does your extract contain maltodextrin or other carriers?

Answer: When necessary for powder stability, yes—but strictly as a functional manufacturing aid, never as a cheap filler for profit. For certain sticky botanicals, maltodextrin is wet-blended before spray drying to prevent caking and ensure flowability. We guarantee 100% formulation transparency by explicitly declaring the exact carrier ratio on every batch CoA, and we fundamentally reject the deceptive industry practice of “dry-blending” cheap carbohydrates into finished powders to artificially slash wholesale prices. For specialized requirements, we also offer custom 100% carrier-free extraction upon request.

Q2: How do you prevent active compound spiking or adulteration?

Answer: We prevent adulteration at the source. First, we bypass untraceable open spot markets and procure raw materials directly from trusted cultivation bases. Second, every incoming batch undergoes TLC (Thin-Layer Chromatography) authentication against Chinese Pharmacopoeia (CP 2020) reference standards before entering extraction. This guarantees that the active markers we quantify via HPLC are 100% naturally derived.

Q3: Where do you source your raw botanical materials?

Answer: We strictly source from globally recognized optimal terroirs (Dao-Di regions). For example, our facility is strategically located in Lushi County, a premier growing region. By processing the raw material close to its origin, we lock in peak phytochemical potency and prevent the degradation that occurs during long-distance raw material transit.

Q4: Do you test every batch, or just randomly sample?

Answer: Every single production lot is rigorously tested in our in-house analytical laboratory before release. We test for target active compounds (HPLC/UV-Vis), heavy metals (AAS), moisture, and microbiological safety. A lot-specific Certificate of Analysis (CoA) is issued with every shipment—we publish the actual measured values, not just minimum claims.

Q5: What quality management certifications does your facility hold?

Answer: Our fully integrated extraction facility operates under strict GMP guidelines and holds comprehensive international certifications, including ISO 9001 (Quality Management), ISO 14001 (Environmental Management), and ISO 45001 (Occupational Health and Safety). We welcome third-party audits from our buyers.

Q6: Is the extract fully soluble in cold water for beverage or veterinary applications?

Answer: Yes. Our specific Nutraceutical and Veterinary grades are engineered for excellent solubility. Thanks to our centrifugal spray drying process and precise solvent routing, the powder disperses rapidly in cold water (typically within 60 seconds) with zero sedimentation, making it ideal for clear functional beverages and automated poultry drinker lines.

Q7: Can you produce custom compound extracts or specific concentrations?

Answer: Absolutely. As a direct manufacturer, we offer full customization. Whether you need a specific active marker concentration, a tailored extraction solvent (water vs. food-grade ethanol), or a multi-herb compound co-extraction (e.g., traditional Yinqiao formulas), our R&D team can scale it from lab validation to commercial production.

Q8: What is the difference between your Cosmetic, Veterinary, and Pharma grades?

Answer: We tailor the extraction parameters for each industry. Pharma Grade features the highest active concentrations and strict CP 2020 compliance. Cosmetic Grade is INCI-compliant, optimized for lighter color (to prevent formulation staining), and strictly controls solvent residues. Veterinary Grade focuses on high heat stability for feed pelleting and excellent water solubility for flock medication.

Q9: What is your Minimum Order Quantity (MOQ) and lead time?

Answer: Standard grades are kept in stock with a 50 kg MOQ for initial commercial orders. Lead time from stock is 5–7 business days. Custom grades or unique enrichment specifications generally require a 4–6 week production lead time.

Q10: How can we request a sample for lab formulation and testing?

Answer: We provide 20-100g samples free of charge for formulation validation. Every sample includes a full CoA and specification sheet. Samples are dispatched within 48 hours of your request via express courier (DHL/FedEx). Freight costs are collected (paid by the buyer) to ensure expedited delivery to the EU, US, and global markets.

Synergistic extracts for compound formulation

The following are most frequently requested alongside Honeysuckle Extract. All available in the same four product forms from the same facility — consistent quality, single-source supply chain.

Forsythia Extract

Forsythia suspensa

Chinese Skullcap Extract

Scutellaria baicalensis

Isatis Root Extract

Isatis indigotica

Astragalus Extract

Astragalus membranaceus

Start with a free 20-100g sample. Ships in 48 hours.

Worldwide express delivery. Every sample ships with a full CoA (HPLC/UV-Vis verified), spec sheet, and a pricing indication for your target volume.

Choose your grade — pharmaceutical, health supplement, veterinary, or cosmetic
CoA reports target active compounds as actual measured values — not just minimum claims
Pricing indication for your MOQ included in the same reply
Formulation calculation sheet and inclusion rate guidance available on request
NDA available before any technical brief or formula disclosure

All inquiries treated with strict confidentiality · No pushy follow-ups · One business day response guaranteed

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We reply within 1 business day with pricing, lead time, and sample tracking number.

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NDA available on request · No commitment required · Confidential