Pharmaceutical Applications
Applications · Pharmaceutical
Pharmaceutical-grade Monk Fruit
for Drug & Supplement Manufacturers
Monk fruit extracts serve as a natural, high-purity excipient for taste masking, palatability improvement and functional sweetening in oral pharmaceutical formulations, OTC products and nutritional supplements — where safety, traceability and documentation are non-negotiable.
GMP Manufactured
Full Batch Traceability
COA & TDS Available
HACCP Certified
Mettler-Toledo Metal Detection
Pharmaceutical Use Cases — Extracts & Concentrates
Where monk fruit ingredients add value in drug and supplement manufacturing
Traditional Chinese Medicine (TCM) Formulations
Added to herbal decoctions and TCM preparations as a co-ingredient to mask bitter herbal flavours and improve palatability. Enhances patient compliance without altering the therapeutic profile.
Flavour PowderV20Concentrate MFJC
Oral Drug & Supplement Taste Masking
Masks bitterness in vitamins, minerals, APIs and herbal actives in liquid syrups, chewable tablets, and dissolvable strips. Creates a pleasant sweet note that improves patient — especially paediatric — acceptance.
V50V60V75
Oral Liquid Preparations
Syrups, oral drops, and liquid supplements for diabetic or weight-conscious patients where sugar is contraindicated. Zero glycaemic impact enables use in glucose-sensitive formulations without reformulation risk.
V50Concentrate MFJQ
Nutritional Supplements (Nutraceuticals)
Gummies, soft gels, chewable lozenges and effervescent tablets — monk fruit extract provides sweetness while keeping the formulation free from sugar, artificial sweeteners and calorie contribution.
V20V50V75
Monk Fruit Juice Concentrate — Pharma & OTC Applications
The MFJC series is particularly suited to throat-soothing and respiratory OTC products
| Product / OTC Category | Recommended Series | Functional Role | Key Properties |
|---|---|---|---|
| Throat lozenges & cough drops | MFJC | Throat-soothing function + sweetening | Rich monk fruit flavour, 15–20× sweetness, anti-inflammatory properties |
| Cough syrup & lung supplements | MFJCMFJF | Taste masking + therapeutic support | Soothes lungs, opens airway, complements herbal APIs |
| Tobacco & nicotine products | MFJC | Reduces combustion tar content | Lowers tobacco oil content, natural additive for harm reduction |
| Paediatric oral medicines | MFJQV50 | Sugar-free taste improvement | GRAS for infant foods · Zero sugar · No artificial additives |
| Diabetic OTC supplements | V60V75 | Zero-GI sweetening excipient | No glycaemic impact · 0 kcal · Compatible with diabetic diet protocols |
Quality Assurance & Documentation
Pharmaceutical buyers require more than just a product — they need full documentation and traceability · View Extracts → | View Concentrates →
GMP Manufacturing
Both production bases operate under GMP standards. All processes comply with HACCP and ISO22000 food safety management systems.
Full Batch Traceability
From contracted farms through extraction and packaging — every batch is traceable. COA issued per batch with complete analytical data.
Solvent Purity
Only purified water and food-grade ethanol used in extraction. Zero industrial solvents. Critical for pharma-grade ingredient acceptance.
Metal Detection
Mettler-Toledo metal detectors plus magnetic grate filters on all production lines — pharmaceutical-standard contamination control.
Available Documents
COA (Certificate of Analysis), TDS (Technical Data Sheet), MSDS, allergen declaration, heavy metals testing, microbial test reports.
Automated Production
Fully automated, digitally controlled lines. Industry-exclusive 80m+ counter-current extraction line ensures batch consistency.
Certifications Relevant to Pharma Buyers
GMP
Good Manufacturing Practice — both bases
HACCP
Hazard analysis critical control point certified
ISO 22000
Food safety management system
BRC
British Retail Consortium — EU/UK markets
USDA Organic
NOP certified — US pharma supply chains
Kosher KOF-K
Certified kosher excipient use
Halal ARA
JAKIM & BPJPH recognised
FSMA-FSVP
FDA food safety compliance for US import
Why Pharma Manufacturers Choose SanLengBio
Regulatory-ready Documentation
Full documentation package ready: COA, TDS, MSDS, allergen & heavy metal reports. Supports your regulatory submissions in US, EU, and Asia-Pacific.
Pharma-compatible Purity
High-purity Mogroside V grades (50%–75%). No industrial solvents. Mettler-Toledo metal detection on all lines. Consistent batch-to-batch specification.
Custom Specification Support
R&D team collaborates on excipient specifications. Custom particle size, sweetness ratio, and blend formulations available for OEM pharma clients.
Multi-regional Compliance
GRAS (US FDA), approved in Australia, NZ, Japan. BRC and ISO22000 for EU. Halal and Kosher for Middle East and global Muslim/Jewish market pharma.
Stable Supply Assurance
300-tonne daily capacity. 33+ years of monk fruit expertise. Contracted farms with government-backed demonstration base ensure raw material security.
Technical & Regulatory Support
Dedicated account support for pharma buyers. Assistance with supplier qualification audits, documentation requests, and application development.
Qualifying a new excipient supplier?
Request a full documentation package (COA, TDS, MSDS) or arrange a supplier qualification audit.
