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FAQs

Q1: What is your core business model?

We operate as a global provider of B2B nutraceutical supply chain services. We support product sourcing, development, manufacturing, quality planning, export-ready packaging, and project delivery. Final scope and deliverables are confirmed based on the specific project requirements.

We offer both:

  • OEM: manufacture based on your confirmed formula/specification.
  • ODM: end-to-end support, including concept, formula, packaging plan, and documentation planning.

IP ownership, confidentiality, and deliverables will be defined in the agreement.

Common formats include tablets, hard capsules, softgels, powders, gummies, and other nutraceutical dosage forms. Availability depends on the ingredient profile, stability, and destination/channel requirements.

MOQ depends on dosage form, packaging, and ingredient complexity. We can support sampling and pilot-scale work first, then move into commercial MOQ. The final MOQ is confirmed after the feasibility assessment.

Yes. We can support sample development and pilot batches for internal evaluation, early market testing, and content creation. Costs and lead times depend on dosage form, formula complexity, and packaging setup.

Timelines vary by project. A common structure is:

  1. requirement confirmation & feasibility review
  2. sampling & iteration
  3. mass production
  4. QC release & shipping
    We will provide a project timeline after confirming your requirements.

Documents are provided on a SKU/destination/channel basis. Common deliverables may include:

  • COA (finished goods and/or raw materials, project-based)
  • specification sheet
  • microbiology/heavy metals testing results (panel determined by risk and destination needs)
  • allergen/GMO statements (if applicable)
  • other documents as required by the project and the destination market

We can support third-party testing arrangements or client-nominated labs where feasible. Testing panels are defined based on ingredient risk profile and destination/channel requirements.

We can support label content preparation and layout guidance (ingredients, directions, warnings). Claims and certain regulatory items may require destination-market review by local compliance experts. Final compliance must follow the destination laws and platform policies.

Origin and “Made in …” statements depend on applicable laws, manufacturing steps, and documentation evidence. We can discuss feasible options and evidence requirements, but final origin claims must follow the destination market’s rules.

Quality planning typically includes raw material controls, in-process checks, finished-product testing (as applicable), batch records, and controlled-release procedures. Specific QC plans are confirmed for each SKU and destination, per requirements.

We can sign an NDA and define IP ownership in the manufacturing agreement. Your formula, artwork, and specifications can be handled under controlled access. Client-only configurations can be supported where applicable.

Yes. We can support packaging configuration aligned with common e-commerce requirements (barcodes, cartons, tamper-evidence, labelling layout). Requirements differ by platform and destination, so details are confirmed before production.

Payment terms depend on order size, customisation level, and cooperation history. Common structures include deposit + balance before shipment, or other arrangements subject to risk assessment and agreement.

Please send:

  1. target market/country
  2. sales channel (Amazon/TikTok/distributor/DTC)
  3. dosage form
  4. ingredient/dosage idea (or your formula)
  5. packaging preference
  6. target MOQ

We will respond with feasibility feedback and a quotation framework.

Ready to Start Your Project?

Whether you choose standard China OEM or hybrid manufacturing, we’re here to support your nutraceutical brand development.

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