Explore our core certified active ingredients developed for maximum bioavailability, clinical efficacy, and absolute regulatory compliance across global manufacturing supply chains.
Chengdu Chenlv Herb Co., Ltd.
Established in 2012, Chengdu ChenLv Herb Co.,Ltd. (referred to as "Chenlv Herb") is a pioneering high-tech enterprise specializing in the research, development, custom manufacturing, and international distribution of botanical extracts and highly refined natural pharmaceutical ingredients.
We are passionately committed to supplying high-purity, standardized natural raw materials that optimize consumer safety and physiological performance. Over the past decade, we have established ourselves as a benchmark supplier serving global pharmaceutical, cosmetic, nutritional supplement, and clinical animal nutrition brands. Under strict regulatory guidelines, including CE compliance, we deliver customized bio-solutions with trace elements analysis, validated bioactivity markers, and clean-label compliance.
Established In
A comprehensive analysis of pharmaceutical and aesthetic market trajectories driving demand for standardized Chamomile extracts.
The global pharmaceutical and clinical skin-care markets are experiencing a significant paradigm shift from raw, unstandardized botanical powders toward high-precision phyto-complexes. Matricaria recutita (German Chamomile) extract has historically been recognized for its anti-inflammatory, spasmolytic, and skin-barrier restorative activities. Modern scientific research has identified key bioactive agents within the plant—chiefly Apigenin (an exceptionally potent flavonoid), Bisabolol, and the blue-pigment sesquiterpene Chamazulene.
For chemical and medical manufacturing buyers, simple herbal extracts are no longer acceptable. The industry demands standardized botanical components that ensure consistent batches. This shift is driving key parameters such as High-Performance Liquid Chromatography (HPLC) verification for flavonoid content and Gas Chromatography-Mass Spectrometry (GC-MS) for volatile sesquiterpene profiles. Standardized extraction ensures that the target biological pathways are activated predictably.
With cosmetic guidelines and natural pharmaceutical frameworks tightening across Europe (such as REACH and the EU Cosmetics Regulation 1223/2009), traceability and purity have become critical competitive factors. Natural products containing impurities, heavy metals, or allergen residues face strict import bans.
Achieving CE Certification signifies that Recutita Extract meets rigorous health, safety, and environmental standards within the European Economic Area (EEA). Specifically, for manufacturers formulating topical ointments, natural medical devices, or clinical-grade cosmetics, CE-certified raw materials ensure streamline registration paths. It assures procurement officers that the phytomedical ingredients are free from harmful pesticide residue (under EC 396/2005 limits), heavy metals (lead, arsenic, mercury, cadmium), and residual solvents.
Conventional solvent extraction methods utilizing hexane or acetone are falling out of favor due to environmental concerns and toxic residues. The global plant extract market is shifting toward eco-efficient extraction methods like Supercritical Fluid Extraction (SFE) using CO₂. This process preserves the volatile, highly sensitive active fractions of Matricaria recutita (especially Bisabolol and Chamazulene) without chemical alteration or heat degradation. Developing solvent-free botanical matrices represents a key target for next-generation product development.
Addressing the core supply chain bottlenecks, raw material specifications, and regulatory hurdles of international enterprise buyers.
Enterprise procurement teams require verified active ingredient percentages (e.g., minimum 1.2% Apigenin by HPLC). We issue complete Certificates of Analysis (COA) and third-party laboratory verification for every batch.
Ensuring raw material compliance with international USP/EP pharmacopoeia requirements. We implement strict testing routines for pesticide residues, mycotoxins, and heavy metals using ICP-MS instrumentation.
Global brands often demand carrier-free extract powders or specific organic carriers like organic maltodextrin. Our facility provides tailored spray-drying, powder micronization, and liquid dilution.
Choose Chenlv Herb for products that deliver beyond expectations through robust R&D, processing technology, and strict quality control.
Creative designs, novel extraction setups, and proprietary formulas that elevate your brand and improve bio-availability.
Fast processing times, state-of-the-art spray drying, and eco-friendly packaging aligned with modern environmental values.
End-to-end cosmetic packaging and raw material solutions designed with environmental footprint reduction in mind.
Fast turnaround, live production tracking, and dedicated regulatory support to meet your strict timeline schedules.
A dedicated QC/QA team supporting you every step of the way with in-house HPLC, GC-MS, and ICP-MS testing equipment.
Over a decade of industry expertise ensuring precise botanical extraction, compliance validation, and logistical excellence.
Integrating botanical active molecules across diverse industries for target-specific consumer products.
Driven by the concept of "homology of medicine and food" and modern health needs, plant extracts have become the core raw materials for dietary supplements, enhancing cellular immunity and sleep quality naturally.
From ancient herbal formulas to modern validated therapeutics, plant extracts occupy a prominent position in clinical pharmaceutical applications due to their precise, multi-target pharmacological mechanisms.
Driven by clean-beauty demands and skin barrier repair sciences, our certified Chamomile extracts deliver highly soothing, anti-inflammatory, and hypoallergenic protection to modern skincare brands.
Offering natural alternatives to synthetic antibiotics, plant extracts show outstanding performance in supporting animal gastrointestinal microflora, reducing stress, and improving overall breeding vitality.
Chenlv Herb provides one-stop contract manufacturing services designed to ensure raw material customization with minimal lead times.
Initial expert consultation to map out raw material specs, active content parameters, and market target certifications.
Comprehensive commercial proposal covering customized target yields, packaging preferences, and logistical estimates.
Legal and quality agreement finalization (including GMP, DMF registration support, and NDA agreements if necessary).
R&D pilot-scale extraction runs to generate custom samples matching the specific chromatography fingerprint of your order.
Following formal client approval of samples, the commercial production run is scheduled at our GMP-certified facility.
Stringent double-check testing of batches (including microbiological profiles, heavy metals, solvent residue) to issue final COA.
Direct delivery to global destinations with custom clearance assistance, localization compliance, and transport monitoring.
Our commitment to botanical intelligence means pushing the boundaries of traditional extraction using advanced chemical engineering and modern AI diagnostics.
As a premium CE-certified Recutita Extract manufacturer, Chengdu Chenlv Herb Co., Ltd. is investing in next-generation analytical platforms. Our 2026-2028 technical development plan outlines three primary strategic trajectories:
Our raw material facility is strictly certified under leading international quality systems to streamline your custom clearance and production registration processes.
Keep up to date with our raw material trends, technology updates, and upcoming botanical conferences.
Recently, the market price of Citrus aurantium raw materials in China has been on the rise, drawing significant attention from the industry. As the new production season (May-June) comes to an end and new supplies gradually enter the market, price fluctuations have become a focal point due to supply and demand dynamics and cost considerations.
As a 'calling card' for leading China's pharmaceutical industry onto the global stage, the 23rd China Pharmaceutical Raw Materials Exhibition (CPHI China 2025) will join hands with the 18th China Pharmaceutical Machinery.
We are thrilled to present our newly certified botanical components at the upcoming 92nd API Conference. Join our technical engineers as we explore custom carrier solutions and standardized active profiles.
In-depth technical answers addressing regulatory, extraction, and standardization concerns for procurement specialists.
Our Matricaria recutita extract is primarily standardized for the flavonoid Apigenin (available in configurations ranging from 1.2% up to 98% pure bio-fractions). Depending on the target industry (e.g., oil-soluble cosmetic formulations), we also standardize the volatile components Alpha-Bisabolol and Chamazulene. All active marker contents are quantified via High-Performance Liquid Chromatography (HPLC) or Gas Chromatography-Mass Spectrometry (GC-MS) to guarantee batch-to-batch therapeutic uniformity.
CE Certification ensures the raw botanical extract complies with the essential health, safety, and environmental protection requirements established under European Directives. For pharmaceutical and medical device manufacturers (such as Class I clinical wound dressings or oral rinses), CE validation provides direct, streamlined entry into the European Economic Area (EEA) markets, confirming the manufacturer maintains a rigorous quality management system compliant with EU regulations.
Yes. We offer fully customizable carrier platforms. We can manufacture extract powder using organic Maltodextrin, Gum Arabic, Microcrystalline Cellulose (MCC), or offer 100% carrier-free options for concentrated capsule formulations. Liquid extracts can also be diluted in specific carrier bases such as cosmetic-grade Butylene Glycol, Glycerin, or Propylene Glycol depending on your exact formulation requirements.
We comply fully with Regulation (EC) No 396/2005 for pesticide residues and established EP/USP limits for heavy metals. Our in-house quality control center operates Inductively Coupled Plasma Mass Spectrometry (ICP-MS) and GC-MS/MS setups. We test every production lot, and third-party laboratory verification (e.g., SGS, Eurofins) is regularly provided alongside our internal Certificate of Analysis (COA) to guarantee complete compliance.
Further active ingredients manufactured under strict GMP compliance, serving international pharmaceutical, veterinary, and nutraceutical brands.
