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Functional Pellets

PelleTune™ Peppermint Oil Enteric Pellets, NLT 15% w/w

Single-active enteric oil pellet designed for volatility, odour, oil leakage and gastric-stage release. NLT 15% w/w peppermint oil; enteric / intestinal.

Technical summary

Key technical information

Product code NG-PEL-004

Active
Peppermint essential oil
Assay / loading
NLT 15% w/w peppermint oil
Release
Enteric / intestinal
Format
Enteric Oil Pellet

Commercial evaluation

Choose an evaluation sample or listed pack where available. Use Request a Quotation for commercial supply and Request Technical Documents for controlled product information.

Evaluation sample price · excl. VAT €45,00

Evaluation samples and selected packs can be ordered online where shown. Use Request a Quotation for commercial supply requirements.

For business buyers. Product-specific documentation and availability are confirmed for each enquiry.

How the sample programme works
100 gEvaluation sample €45,00

Product information

PelleTune™ Peppermint Oil Enteric Pellets, NLT 15% w/w — Technical and commercial details

Review the key specifications at a glance, then expand only the sections you need.

Single-active enteric oil pellet designed for volatility, odour, oil leakage and gastric-stage release. NLT 15% w/w peppermint oil; enteric / intestinal.

Peppermint Oil Enteric Pellets, NLT 15% w/w supplies Peppermint essential oil in a multi-unit functional pellet with a product-specific food-grade coating system. It is intended as an independent formulation module for professional B2B use. Product-specific identity, assay, physical, microbiological, contaminant and stability controls are defined in the finished-product specification and verified by batch CoA.

What is Peppermint Oil Enteric Pellets, NLT 15% w/w?

Peppermint Oil Enteric Pellets, NLT 15% w/w supplies Peppermint essential oil at NLT 15% w/w peppermint oil in a multi-unit functional pellet with a product-specific food-grade coating system; its release behaviour is Enteric / intestinal.

Product ID / order SKU NG-PEL-004
Technology Functional Pellets
Product type Enteric Oil Pellet
Current status Qualification and availability confirmed per enquiry
Active / marker Peppermint essential oil
Assay / loading NLT 15% w/w peppermint oil
Delivery system multi-unit functional pellet with a product-specific food-grade coating system
Release type Enteric / intestinal
Evaluation sample 50 g — €35 ex VAT
Commercial MOQ Confirmed per quotation
Pack sizes 1 kg; 5 kg; 25 kg
Lead time Confirmed per quotation

What is the technical specification?

The key public specification is NLT 15% w/w peppermint oil with Enteric / intestinal release behaviour; batch acceptance follows the approved product-specific specification and analytical method.

Active ingredient Peppermint oil
Chemical / nutrient form Peppermint essential oil
Assay / loading NLT 15% w/w peppermint oil
Assay method Approved product-specific analytical method
Carrier / wall material Food-grade pellet core, binder and product-specific functional coating
Delivery system multi-unit functional pellet with a product-specific food-grade coating system
Release behaviour Enteric / intestinal
Particle size d10 Per specification
Particle size d50 Per specification
Particle size d90 Per specification
Mesh range 500–850 µm target; controlled specification governs
Bulk density Per specification
Tapped density Per specification
Moisture / loss on drying Per specification
Water activity Per specification
Solubility Product-specific; see TDS
Dispersibility Product-specific; see TDS
Flowability Per finished-product specification
Appearance / colour Product-specific; see TDS
Odour Product-specific; see TDS
Taste Product-specific; see TDS
pH Not applicable unless specified
Microbiological limits Per finished-product microbiological specification
Heavy-metals limits Per finished-product heavy-metals specification
Residual solvents Complies with finished-product specification
Oxidation markers Product-specific oxidation or degradation markers per finished specification
Other critical specification Dissolution/release profile, coating integrity and friability
Shelf life Per current stability documentation

What is the public composition?

The public composition identifies Peppermint oil with a Food-grade pellet core, binder and product-specific functional coating; exact proprietary excipient ratios and supplier details remain controlled.

Component Function Public composition information
Peppermint oil Active ingredient Product-specific qualified source; NLT 15% w/w peppermint oil; Finished-product specification
Food-grade pellet core / binder system Pellet formation and mechanical integrity Qualified food-grade source; q.s.; Controlled composition; exact proprietary composition is confidential
Product-specific functional coating system Gastric resistance and intestinal release Qualified food-grade source; q.s. to 100%; Controlled composition; exact proprietary composition is confidential

Country of origin is stated in the controlled Country of Origin Statement. Supplier and manufacturing-site information are not published.

Which formulation problem does this ingredient address?

A multi-unit pellet architecture separates the active from the formulation environment and delivers the defined enteric / intestinal behaviour.

  • Defined enteric / intestinal performance
  • multi-unit dosing
  • coating-based protection
  • blend-compatible target size.

Which applications are the best fit?

This ingredient is best suited to hard capsules and multi-unit enteric pellet systems.

How should formulators process and evaluate it?

  • Blend with pellet populations of compatible particle size and bulk density. Avoid milling, crushing or compression conditions that damage the functional coating.
  • Do not mill or open the coating system. Check segregation risk when blending with powders or pellets of materially different size or density.
  • Confirm process compatibility, uniformity, stability and performance in the final matrix.

How is performance verified?

Performance is verified using approved product-specific methods and the controlled evidence listed below.

Test / study Result summary Evidence
Identity and assay confirmation Conforms to approved specification Current commercial batch; Batch CoA
Dissolution / release profile Conforms to approved dissolution / release criteria Representative batch; Dissolution / Release Data
Stability and sensory verification Meets approved stability and product-specific sensory criteria Representative stability batches; Stability Documentation

How should it be stored and handled?

Store tightly closed in original packaging in a cool, dry place, protected from heat, moisture and direct light. Product-specific sensory or odour-control information may be available and is confirmed on request. Performance must be confirmed at the customer’s intended dose and in the final matrix.

Which technical and quality documents can be requested?

The current product-specific document set is confirmed for each enquiry according to qualification status, the applicable manufacturer and relevant batch. Controlled composition, characterisation or performance details may require an NDA where specified.

  • Technical Data Sheet (TDS)
  • Finished Product Specification
  • Batch Certificate of Analysis (CoA)
  • Safety Data Sheet (SDS)
  • Allergen Statement
  • GMO Statement
  • Irradiation Statement
  • BSE/TSE Statement
  • Stability Documentation
  • Composition / Ingredient Information
  • Storage & Handling Information
  • Microbiological Specification
  • Heavy Metals Specification
  • Country of Origin Statement
  • Manufacturing / Quality Certificate
  • Dissolution / Release Data
  • Sensory / Taste-Masking Data

What must buyers confirm for regulatory and intended use?

Regulatory suitability depends on the intended use, dose and target market; the customer must confirm finished-product compliance.

Target market European Union / EEA
Intended use Food supplements and professional formulation use; final suitability depends on dose and application
Ingredient legal status Product-specific ingredient-level information can be confirmed; the customer must verify intended use and national requirements
Novel food review Product-specific regulatory-status information is confirmed on request
Carrier / additive compliance All carriers, wall materials and coating components reviewed for the intended product scope
Maximum / recommended use level Set by customer formulation, applicable law and product-specific technical guidance
Label declaration Peppermint oil
Allergen declaration Declare according to the current product-specific allergen statement
Origin declaration See Country of Origin Statement
Nutrition / health claim relevance Finished-product nutrition or health claims are the customer’s responsibility
Technical claim / statement Functional pellet with defined enteric / intestinal performance.
Evidence supporting statement TDS, specification, stability and dissolution/release data
Medicinal / disease wording check Passed: no medicinal or disease-treatment wording
Regulatory approval status Ready for product-specific website approval

How can B2B buyers evaluate and order it?

  • Evaluation sample: 50 g — €35 ex VAT.
  • May be credited once against the first commercial order for the same legal customer and product/project within 12 months
  • Commercial MOQ is confirmed per quotation.
  • Standard formats: 1 kg; 5 kg; 25 kg.
  • Lead time is confirmed per quotation and depends on product and batch status, quantity, packaging, testing and release requirements, and destination.
  • Custom strength available: Yes, subject to feasibility.
  • Custom release available: Yes, subject to development and validation.
  • Private label / custom pack: Custom pack by quotation.
  • Commercial terms confirmed by quotation.

What does NexaGens not claim?

No medicinal, disease-treatment or finished-product health claim is made. The stated release or protection function applies only when pellet integrity is maintained and the finished dosage form is validated. Finished-product classification, dose, permitted use, label declarations, nutrition or health claims and market compliance remain the customer’s responsibility.

Frequently asked questions

Which documentation can be requested?

The current product-specific document set is confirmed on request according to qualification status, the applicable manufacturer and relevant batch. Where available, product-specific dissolution or release data support the stated pellet function.

Can this product be combined with other ingredients?

Yes. This product may be combined with other independent NexaGens formulation modules after compatibility and finished-product validation.

What is the release format?

The release format is enteric / intestinal.

For professional B2B food, food-supplement and formulation use only. Not for direct consumer use.

Need the controlled document package?

Request the current technical, quality, stability and compliance documents for this ingredient.

Request Technical Documents

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Review the formulation challenges most relevant to this ingredient before requesting evaluation material or documentation.

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