FREEZE DRIED ROYAL JELLY POWDER

Key Functions

Specifications

Form

Powder

Standardization

기능성내용Health Claims

Origin

Australia

Manufacturer

Shared once the supplier is confirmed

Individually approved

No

* Origin and manufacturer are selected among multiple suppliers depending on order volume and specification, so they are not fixed on this page. Once confirmed, the COA and test report are provided together.

Certifications

Technical Documents

Quality documents are provided on request for security reasons.

Frequently asked questions

What is the difference between a notified functional ingredient and an individually approved one?

A notified ingredient already has its specification and daily intake listed in the Korean Health Functional Food Code, so it can be used without a separate approval process as long as manufacturing follows the Code. An individually approved ingredient was approved by the MFDS on a specific company's own dossier, so only that company and its supply chain may use it. This ingredient (FREEZE DRIED ROYAL JELLY POWDER) is a notified ingredient.

What is the basis for the stated specification and daily intake?

The Korean Food Code standard for notified functional ingredients. The value stated for this ingredient is "기능성내용Health Claims". If your product design falls outside this range, the labelling and advertising requirements must be re-checked.

Does the stated specification apply to the finished product as well?

It is a raw-material specification and differs from the finished-product specification. Final content varies with dosage form (tablet, capsule, powder, liquid), excipient ratio, and blending with other ingredients, so the product specification is fixed after the supplier COA and the blend design are confirmed.

Can we receive the COA and test report in advance?

Yes. Request them from the Technical Documents section on this page and our team will reply. For verified business customers we also provide the specification sheet, COA, manufacturing process chart, and allergen information.

Can we get a sample?

Yes. Submit a sample request and we will confirm the intended use (dosage form, target content, development stage) before guiding you. If it is for blending tests, telling us the target dosage form makes our reply faster.

What is the minimum order quantity?

It varies with dosage form, specification, and packing unit, so we do not publish a fixed figure. Tell us your development stage (sample, pilot, mass production) and target volume and we will reply with a quote matched to those conditions. Small development volumes are also open for discussion.

What does the OEM/ODM process look like?

Ingredient confirmation → blend and dosage-form design → sample production → specification and document confirmation (COA, test report) → labelling review → mass production. Sharing your target dosage form and launch schedule at the inquiry stage lets us compress the later steps.

Can this be supplied for export?

Yes. Required documents differ by the importing country's regulations (certificate of free sale, ingredient specification comparison, labelling requirements), so please tell us the target country for accurate guidance. Overseas shipping quotes are handled through the same form.

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