1. Muira Puama Extract Powder Supplier & Manufacturer | GMP Facility | Bulk / Wholesale | Standardized Botanical Grade
AIHerba supplies Muira Puama Extract Powder (Ptychopetalum olacoides) for global B2B buyers who require consistent quality, documented compliance, and reliable lead times. As a GMP-certified manufacturer, we support bulk and wholesale procurement, contract manufacturing, and OEM/ODM projects for supplement, cosmetic, and functional food brands. Each lot can be provided with COA, TDS, and SDS/MSDS, along with batch traceability and contaminant control testing aligned with common USP/EP/ISO approaches.
If you are evaluating suppliers, request a specification sheet, confirm your target grade (extract ratio / standardized markers / carrier-free options), and tell us your MOQ and destination market to receive a fast quotation and logistics plan.
CTA: Contact us to request COA, technical specifications, and pricing for bulk orders and OEM development.
Quick Summary
- Ingredient name: Muira Puama Extract Powder
- Main applications: Capsules/tablets, powder blends, functional beverages (as appropriate), cosmetic formulations (supportive functional ingredient)
- Typical purity: Carrier-free extract powder (customizable with carriers upon request); specification defined by extract ratio and QA limits
- Suitable industries: Dietary supplement brands, contract manufacturers, functional food producers, cosmetics OEM/ODM, ingredient distributors
2. What Is Muira Puama Extract Powder?
Muira Puama Extract Powder is a concentrated botanical ingredient produced from Muira Puama (commonly referenced as Ptychopetalum olacoides). It is manufactured through controlled extraction and drying to deliver a stable powder suitable for industrial formulation. For professional procurement, the key decision points are botanical authentication, plant part, extract solvent system, and the specification model (e.g., extract ratio and/or standardized markers).
Benefits (Regulatory-Safe, Non-Medical)
- Commonly selected for functional positioning in vitality-focused formulations where brands need a recognizable botanical story.
- Offers formulation versatility as a dry powder for blends, capsules, and tablets (and selected beverage applications depending on solubility/processing).
- Supports quality-focused product development via document packages (COA/TDS/SDS) and batch traceability.
Applications
- Dietary supplements: capsules, tablets, stick packs, powdered blends
- Functional foods & beverages: dry mixes, instant products (grade-dependent)
- Cosmetics: botanical complex in targeted formulations (claims must remain cosmetic/appearance-focused)
Dosage / Specification (Procurement-Oriented)
- Specification is purchase-defined (e.g., 10:1, 20:1, or standardized marker request).
- For OEM/ODM programs, define: target extract grade, carrier policy (carrier-free vs. with excipient), particle size, and contaminant limits for destination market compliance.
Muira Puama is supplied as a raw material for industrial use. It is the buyer’s responsibility to confirm suitability for their end-use, labeling, and claims in the destination market. We do not provide medical claims. Safety is addressed through identity testing, contaminant control, and documentation (COA/SDS).
Supplier / Manufacturer (What B2B Buyers Should Verify)
- Botanical identity and plant part verification (incoming raw material inspection)
- COA parameters and test methods (USP/EP/ISO alignment where applicable)
- Batch traceability, retention samples, and change control
- Lead time, MOQ flexibility, and document turnaround time
3. Detailed Technical Specifications
Table 1. Core Specifications (Typical for B2B Procurement; Customizable by Project)
| Item | Specification / Options |
|---|---|
| Product name | Muira Puama Extract Powder |
| Botanical name (reference) | Ptychopetalum olacoides (Muira Puama) |
| Plant part | Available upon request (must be specified on PO) |
| Appearance | Fine powder (color may vary by lot due to natural variability) |
| Odor / taste | Characteristic botanical |
| Extraction solvent | Water/Ethanol system or customized (project-defined) |
| Extract grade | Common options: 10:1, 20:1 (or customized grade) |
| Carrier | Carrier-free (default) or with excipient upon request |
| Particle size | Typically 80–100 mesh (customizable) |
| Loss on drying | ≤ 5.0% (typical target) |
| Total ash | ≤ 5.0% (typical target) |
| Bulk density | Project-defined (provided in TDS) |
| Solubility | Grade-dependent; confirm for beverage/instant applications |
| Heavy metals | Controlled per buyer requirements (see QC tables) |
| Microbiology | Controlled per buyer requirements (see QC tables) |
| Document package | COA, TDS, SDS/MSDS; allergen statement as applicable |
| Shelf life | Typically 24 months in sealed packaging (see Section 11) |
4. Product Source & Raw Material Origin
AIHerba sources raw botanical material through qualified supply channels with an emphasis on:
- Supplier qualification and audits (where applicable)
- Incoming inspection: organoleptic checks, moisture screening, and identity verification
- Traceability controls: lot coding from raw material receipt through finished-goods release
For procurement, specify your required origin preference, documentation requirements, and any restricted substances lists to ensure alignment with your internal compliance program.
5. Mechanism of Action & Functional Properties (Non-Medical)
Muira Puama is commonly positioned as a botanical with functional attributes relevant to:
- Botanical complexity (multi-component extract profile typical of plant extracts)
- Formulation role as a supportive ingredient in multi-botanical blends
- Standardization approach (when requested) to improve batch-to-batch consistency
This section is provided for formulation context only and does not imply disease-related outcomes.
6. Application-Relevant Benefits (Regulatory-Safe)
- Consistency for manufacturing: defined extract grade, controlled moisture, and documented QA limits
- Procurement confidence: COA parameters, method references, and traceability support
- Market flexibility: suitable for supplement and cosmetic supply chains with appropriate documentation
- OEM readiness: packaging options, private label support, and change-controlled production
7. Usage Guidelines & Formulation Recommendations
For supplement manufacturing
- Prefer capsule/tablet-friendly grades with controlled flowability and particle size.
- For tablets, request guidance on compressibility and excipient compatibility.
For powder blends
- Choose particle size aligned with your blend uniformity targets (e.g., 80–100 mesh).
- Use controlled humidity handling to protect stability and prevent clumping.
For beverage / instant mixes
- Confirm solubility and dispersibility requirements early. Many botanical extracts require processing adjustments (agglomeration, carriers, or instantization).
For cosmetics
- Define your target INCI/labeling approach (region-specific).
- Ensure claims remain cosmetic (appearance-focused) and are reviewed by your regulatory team.
8. Traditional & Modern Industrial Applications
- Traditional context: Muira Puama has a long history of regional use as a botanical.
- Modern industry use: Today it is primarily procured as an ingredient for brand storytelling, botanical blend design, and category positioning in supplement and cosmetic formulations—supported by documented QC controls and standardized procurement specs.
9. COA & Quality Control Specifications
Below is a procurement-friendly QC structure commonly requested for bulk/wholesale botanical extracts. Final limits should be confirmed based on destination market, customer specs, and product grade.
9.1 Pesticide Residues
| Pesticide residue item | Limit | Test method |
|---|---|---|
| Organochlorines (sum, screening) | ≤ 0.01 mg/kg | GC-MS/MS |
| DDT (sum) | ≤ 0.01 mg/kg | GC-MS/MS |
| BHC (sum) | ≤ 0.01 mg/kg | GC-MS/MS |
| Aldrin & Dieldrin (sum) | ≤ 0.01 mg/kg | GC-MS/MS |
| Organophosphates (screening) | ≤ 0.01 mg/kg | GC-MS/MS |
| Chlorpyrifos | ≤ 0.01 mg/kg | GC-MS/MS |
| Malathion | ≤ 0.01 mg/kg | GC-MS/MS |
| Pyrethroids (screening) | ≤ 0.01 mg/kg | GC-MS/MS |
| Cypermethrin | ≤ 0.01 mg/kg | GC-MS/MS |
| Permethrin | ≤ 0.01 mg/kg | GC-MS/MS |
9.2 Heavy Metals
| Heavy metal item | Limit | Test method |
|---|---|---|
| Lead (Pb) | ≤ 3.0 ppm | ICP-MS (USP <233> aligned) |
| Arsenic (As) | ≤ 1.0 ppm | ICP-MS (USP <233> aligned) |
| Cadmium (Cd) | ≤ 1.0 ppm | ICP-MS (USP <233> aligned) |
| Mercury (Hg) | ≤ 0.1 ppm | ICP-MS (USP <233> aligned) |
9.3 Microbiological Specification
| Microbial item | Limit | Test method |
|---|---|---|
| Total plate count | ≤ 10,000 CFU/g | USP <2021> / ISO 4833 (as applicable) |
| Yeast & mold | ≤ 1,000 CFU/g | USP <2021> / ISO 21527 (as applicable) |
| Enterobacteriaceae | ≤ 100 CFU/g | ISO 21528 (as applicable) |
| E. coli | Negative / 10 g | USP <2022> / ISO 16649 (as applicable) |
| Salmonella | Negative / 25 g | USP <2022> / ISO 6579 (as applicable) |
| Staphylococcus aureus | Negative / 10 g | ISO 6888 (as applicable) |
Quality control notes
- Batch coding + retention sampling supports traceability and investigations.
- QC release is based on identity, purity, safety, and documentation completeness.
- Project-specific limits can be tightened for regulated channels or sensitive formulations.
10. Manufacturing Process & Production Flow
A robust B2B manufacturing flow typically includes:
- Supplier qualification & raw material intake (documentation review + visual inspection)
- Incoming QC (identity screening, moisture control, contaminant risk check)
- Milling / size reduction (controlled to protect extraction efficiency)
- Extraction (validated solvent system; time/temperature control)
- Filtration & clarification (removes insolubles; improves downstream stability)
- Concentration (standardizes solids content)
- Drying (spray-drying or equivalent; moisture control critical)
- Sieving / blending (mesh consistency; optional carrier adjustment per spec)
- Final QC release (COA + documentation pack)
- Packaging (sealed, labeled, lot-coded) and shipment
11. Storage, Shelf Life & Packaging
Storage
- Store in cool, dry conditions, away from direct sunlight and strong odors.
- Keep sealed to prevent moisture pickup.
Shelf life
- Typically 24 months from production date when stored in unopened, sealed packaging under recommended conditions.
Packaging options (B2B)
- 1 kg aluminum foil bag (sample / pilot)
- 5–10 kg bag-in-carton (project-based)
- 25 kg fiber drum / carton drum (bulk export standard)
- OEM/ODM packaging and labeling available upon request
12. MOQ, Sample Policy & Global Shipping
MOQ
- Standard MOQ is typically project-defined (commonly starting from 10 kg for many extract powders; confirm per grade and packaging).
Sample policy
- Pre-shipment sample or development sample can be arranged for qualified B2B buyers. Provide your target spec and application to receive a suitable grade.
Lead time
- Depends on grade, packaging, and documentation requirements. Share your target delivery date and destination to receive a confirmed production + logistics schedule.
Global shipping
- Export packaging, lot coding, and document sets prepared for international trade. Incoterms and route options can be offered based on your destination and clearance preferences.
13. Clinical Data & Scientific Research (Reference Only, No Medical Conclusions)
Muira Puama appears in scientific literature primarily in contexts such as phytochemical characterization, botanical studies, and formulation-related discussions. For buyer evaluation, we recommend reviewing primary literature and conducting your own regulatory assessment for claims and labeling in the destination market.
Suggested literature entry points:
- PubMed search: “Muira Puama Ptychopetalum olacoides phytochemistry”
- PubMed search: “Ptychopetalum olacoides extract study”
(References are provided in Section 19.)
14. Applicable Industries
- Dietary supplement brands (capsules, tablets, blends)
- Contract manufacturers (GMP manufacturing, batching, encapsulation/tableting)
- Functional food producers (dry mixes, instant products—grade-dependent)
- Cosmetic manufacturers and brand owners (appearance-focused claims only)
- Ingredient distributors and importers (bulk/wholesale supply)
15. Industry Application Scenarios (Realistic B2B Use Cases)
Scenario 1: Men’s vitality supplement brand (capsules)
- Buyer need: consistent extract grade, clean micro limits, stable supply for quarterly production
- Recommended approach: carrier-free 10:1 or project-defined standardized grade; 80–100 mesh; full COA + SDS
- Procurement focus: batch-to-batch consistency, lead time reliability, private label support
Scenario 2: Contract manufacturer building a multi-botanical tablet
- Buyer need: tabletability, blending uniformity, controlled moisture
- Recommended approach: controlled particle size + optional excipient strategy; provide flowability and compressibility data where available
- Procurement focus: change control, traceability, and documentation readiness for audits
Scenario 3: Cosmetic OEM developing a botanical scalp/skin support formula
- Buyer need: ingredient story + contaminant controls + cosmetic-safe documentation
- Recommended approach: define cosmetic-use documentation pack and claims boundaries; supply COA, SDS, and allergen statement (as applicable)
- Procurement focus: regulatory-safe claims, supply continuity, and packaging suitable for OEM workflows
16. Supplier Comparison & Procurement Guide
How to compare suppliers (practical checklist)
- Identity assurance: botanical name, plant part, authentication method, adulteration risk management
- Specification clarity: extract ratio and/or standardized markers; moisture/ash limits; particle size
- COA transparency: clear parameters + methods (GC-MS/MS, ICP-MS, USP/ISO references)
- Traceability: lot coding, retention samples, deviation handling
- Regulatory readiness: SDS/MSDS, TDS, allergen statements, compliance support
- Commercial execution: MOQ flexibility, lead time, packaging options, export documentation
17. FAQ for B2B Buyers (6)
- What grades do you offer (10:1, 20:1, standardized)?
We can supply common extract ratios (e.g., 10:1, 20:1) and discuss project-defined specifications. Request the TDS to match your application. - Do you provide COA, TDS, and SDS/MSDS for each batch?
Yes. A full document set can be provided to support supplier qualification and incoming QC. - How do you control batch-to-batch consistency?
Through controlled raw material intake, defined processing parameters, in-process checks, and final QC release tied to lot coding and traceability. - What is your MOQ and sample policy?
MOQ is project-defined (often starting from small bulk quantities for evaluation). Samples can be arranged for qualified B2B buyers based on target specification and application. - Can you support OEM/ODM manufacturing?
Yes. We support bulk supply and OEM/ODM programs, including packaging options and documentation support. - What is the typical lead time and shipping method?
Lead time depends on grade, packaging, and documentation. Provide destination and target date for a confirmed production and shipping plan.
19. References & Regulatory Sources
Below are reputable reference entry points for scientific literature and regulatory frameworks.
PubMed (NIH) – Search (Muira Puama / Ptychopetalum olacoides):
https://pubmed.ncbi.nlm.nih.gov/?term=Muira+Puama+Ptychopetalum+olacoides
https://pubmed.ncbi.nlm.nih.gov/?term=Ptychopetalum+olacoides+extract
NIH – National Center for Complementary and Integrative Health (general supplement safety context):
https://www.nccih.nih.gov/health
US FDA – Dietary Supplement cGMP (21 CFR Part 111):
https://www.ecfr.gov/current/title-21/chapter-I/subchapter-B/part-111
US FDA – Dietary Supplements (labeling / regulatory overview):
https://www.fda.gov/food/dietary-supplements
USP – Elemental Impurities (commonly referenced methods: <232>/<233>):
https://www.usp.org/compounding/general-chapter-elemental-impurities-procedures
(USP access and chapter viewing may require subscription; confirm via your USP resources.)
EU – General Food Law (Regulation (EC) No 178/2002):
https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:32002R0178
EU – Maximum Residue Levels of pesticides (Regulation (EC) No 396/2005):
https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:32005R0396
EU – Contaminants in food (Regulation (EU) 2023/915):
https://eur-lex.europa.eu/eli/reg/2023/915/oj
WHO – Good Agricultural and Collection Practices (GACP) for medicinal plants:
https://www.who.int/publications/i/item/9241546271
Manufacturer & Quality Assurance
Manufactured by AIHerba® (Shaanxi Zhonghong Investment Technology Co., Ltd.),
a GMP-certified manufacturer specializing in high-purity botanical extracts
for dietary supplements, cosmetics, and pharmaceutical applications.
✔ GMP-certified production facility
✔ Full COA & technical specifications available
✔ Batch traceability & strict quality control
✔ Bulk supply & OEM/ODM services for global B2B buyers
📧 sales@aiherba.com
| info@aiherba.com
| liaodaohai@gmail.com
🌐 www.aiherba.com
If you are looking for a bulk supplier / OEM manufacturer of Muira Puama Extract Powder, contact us for specifications, COA, and pricing.
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