Product Introduction
Customized Blend Mushroom Capsules are dietary supplements formulated with standardized mushroom extracts, such as Reishi, Lion's Mane, and Cordyceps, designed to support immune function, cognitive health, and overall wellness.
We supply these capsules as both finished dietary products and as a scalable OEM/ODM service, providing end-to-end support from raw material sourcing and formulation development to manufacturing and global regulatory compliance.
Formula
|
Ingredient |
Standardization |
Primary Health Benefit |
|
Reishi Extract |
30% Polysaccharides |
Immune support & stress adaptation |
|
Lion's Mane Extract |
30% Polysaccharides |
Cognitive function, memory & nerve health |
|
Cordyceps Extract |
7% Cordycepic Acid |
Energy, stamina & athletic performance |
|
Chaga Extract |
30% Polysaccharides |
Antioxidant defense & cellular health |
|
Shiitake Extract |
30% Polysaccharides |
Cardiovascular & immune system support |
Other Ingredients: Vegetable Cellulose(capsule), Microcrystalline Cellulose, Magnesium Stearate Silicon Dioxide
Directions: Take one capsule twice daily with water, preferably with a meal, or as directed by a healthcare professional.
Technical Specifications
|
Raw Material |
Blend Mushroom Powder |
|
Assay |
40% Polysaccharide |
|
Capsule shell |
Gelatin or Vegetarian Capsules |
|
Capsule Size |
0# / 1# / Custom Size |
|
Label Material |
PVC, Synthetic paper |
|
Dosage |
500mg/ Custom Dosage |
|
MOQ |
Flexible, starting from 500 units |
|
Shelf Life |
24 months under proper storage |
|
Certificates |
GMP, ISO, COA, Third-party Testing |
|
Lead Time |
Stock Formula:3 days Custom Formula:7 days |
Rigorous Quality Control
Each batch is accompanied by comprehensive testing results to satisfy international regulatory bodies.
Testing Standards:
- Identification: Conforms with TLC standards.
- Heavy Metal Screening: ICP-MS verification for Lead, Arsenic, Cadmium, and Mercury.
- Microbiological Safety: AOAC-method testing for total plate count, yeast/mold, E.Coli, and Salmonella.
- Potency Verification: UV/HPLC analysis to ensure label claim accuracy.
|
Item |
Specification |
Result |
Method |
|
General Information |
|
|
|
|
Product Name |
Reishi Mushroom Extract |
|
|
|
Physical and Chemical Property |
|
|
|
|
Appearance |
Brown Powder |
Conforms |
Visual |
|
Particle Size |
≥95% through 80 mesh |
Conforms |
Screening |
|
Residue on Ignition |
≤5g/100g |
3.52g/100g |
3g/550℃/4hrs |
|
Loss on Drying |
≤5g/100g |
3.05g/100g |
3g/105℃/2hrs |
|
Identification |
Conforms with TLC |
Conforms |
TLC |
|
Content |
≥30% Polysaccharides |
Conforms |
UV |
|
Residue Analysis |
|
|
|
|
Heavy Metals |
≤10mg/kg |
Conforms |
- |
|
Lead (Pb) |
≤3.00mg/kg |
Conforms |
ICP-MS |
|
Arsenic (As) |
≤2.00mg/kg |
Conforms |
ICP-MS |
|
Cadmium (Cd) |
≤1.00mg/kg |
Conforms |
ICP-MS |
|
Mercury (Hg) |
≤0.50mg/kg |
Conforms |
ICP-MS |
|
Microbiological Tests |
|
|
|
|
Total Plate Count |
≤1000cfu/g |
200cfu/g |
AOAC 990.12 |
|
Total Yeast & Mold |
≤100cfu/g |
10cfu/g |
AOAC 997.02 |
|
E.Coli. |
Negative/10g |
Conforms |
AOAC 991.14 |
|
Salmonella |
Negative/10g |
Conforms |
AOAC 998.09 |
|
S.aureus |
Negative/10g |
Conforms |
AOAC 2003.07 |
Our Manufacturing Capabilities
Beyond individual product customization, we leverage a comprehensive supply chain and diverse formulation capabilities to support your entire product line.
Premium Raw Material Sourcing
We maintain a reliable supply of high-purity mushroom powders, processed to precise particle sizes for optimal blending and encapsulation.
|
Raw Material |
Specification |
|
Cordyceps Militaris / Shiitake / Maitake / Chaga / Lion's Mane |
80 Mesh |
|
White Fungus Powder |
100 Mesh |
|
Reishi Powder |
120-150 Mesh |
|
Ganoderma Lucidum Spore Powder (99%) |
200 Mesh |
Flexible Custom Formulation Solutions
We offer versatility in delivery formats and standardization. Tailor your product efficacy and texture to match your specific brand positioning.
- Format Options: Capsules, Powder, Gummies, and Softgels.
- Standardization Flexibility: We adjust active compounds (Polysaccharides, Triterpenes, Beta-Glucans) to meet your specific clinical or market requirements.
|
Extract Type |
Active Compound Standardization Options |
|
Reishi / Chaga |
Polysaccharides 10-50%, Triterpenes 1-3%, Beta Glucan 20-30% |
|
Lion's Mane |
Polysaccharides 20-50%, Beta Glucan 20-35% |
|
Shiitake |
Lentinan 10-50%, Beta Glucan 10-40% |
|
Cordyceps Militaris |
Polysaccharides 10-50%, Cordycepin 0.1-10% |
Strict Quality Control
Every raw material undergoes rigorous screening before entering our manufacturing stream. Our multi-stage QC ensures consistency from raw powder to finished product.

Efficient Global Logistics
We provide streamlined global logistics with full end-to-end documentation support. Our shipping services include comprehensive customs clearance paperwork (Commercial Invoice, Packing List, COA, and Origin Certificates) to ensure smooth delivery to your destination warehouse.

How to Partner with Us
Consultation: Share your target market and specific health claim requirements.
Formula Confirmation: Finalize your custom potency and ingredient blend.
Facility & Sample Approval: Verify product quality via pre-production samples.
Contracting: Sign official manufacturing and quality agreements.
Precision Production: High-speed manufacturing under GMP/ISO certified environment.
Global Delivery: Secure, timely logistics support with complete customs documentation.

FAQ
Q: What is your minimum order quantity (MOQ)?
A: We offer flexible production capabilities starting from 500 units, suitable for both market testing and scalable commercial distribution.
Q: How do you ensure product quality and consistency?
A: We implement strict quality control protocols, including HPTLC identification, heavy metal testing (ICP-MS), and microbiological analysis for every batch. Each order is delivered with a detailed Certificate of Analysis (COA).
Q: Can you assist with global regulatory compliance?
A: Yes. We provide the necessary technical documentation, including COAs, manufacturing flowcharts, and compliance statements to support your product registration in international markets.
Q: What is your typical lead time?
A: For stock formulas, the lead time is approximately 3 days. For custom formulations requiring specific ingredient sourcing or branding, the lead time is approximately 7 days.
Q: How can we verify your facility standards?
A: We operate under GMP and ISO-certified conditions. We welcome client facility audits and can provide our audit documentation or schedule a virtual facility tour upon request.
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