Can I request a sample before placing an order?

Yes. Sample requests go through the quote form. Lead time and sample format depend on packaging and any custom flavour or colour work.

MOQ is confirmed per project. Standard white-label gummy MOQ starts at 1,000 units; doypack and fully custom configurations may carry a higher tier.

Which markets is this product suitable for?

Market eligibility depends on the labelling, claims and certifications required for your destination — reviewed per project against the relevant EU / UK / non-EU framework.

Do you provide a Certificate of Analysis?

A batch-specific Certificate of Analysis is provided after production and QC release. COA scope (microbiological, heavy metals, actives) is agreed up-front in the spec sheet.

Can the formula be customised?

Common adjustments include flavour, colour, sugar profile and packaging count. Active-ingredient changes are evaluated against EU food-supplement rules and may move the SKU into a custom-formula tier.

How long are typical lead times?

Lead time is confirmed in the quote. It depends on raw-material availability, packaging, artwork sign-off and the production calendar at the time of order.

Joint & Bone

Calcium 600 + Vitamin D3 Tablet

Private-label compressed-tablet supplement format. Finish (uncoated, film-coated, chewable) and dose load reviewed per project.

Claim wording reviewed per target market
Batch-release documents after production and QC release
Documentation reviewed against your target market

About this product

Private-label compressed-tablet supplement format. Finish (uncoated, film-coated, chewable) and dose load reviewed per project.

Final claims, documentation and market suitability are reviewed per target market and project scope.

Format considerations

Tablet formulation considerations

Format definition

Compressed tablet. Finish (uncoated, film-coated, chewable), tablet size and pack count are confirmed in the spec sheet.

Compression & finish review

Compression profile, hardness and finish are reviewed against the brief and the target market.

Documentation route

Specification, allergen statement and the per-batch Certificate of Analysis follow the documentation-by-stage path below. Batch-release documents are issued after production and QC release. Final scope depends on product, market and project stage.

Common use cases

How brands typically position this

Brand range expansion

Slot Calcium 600 + Vitamin D3 Tablet into an existing supplement range as a tablet SKU, with shared brand artwork direction and a per-SKU specification.

Adult daily-routine positioning

Pack copy positioned as part of an adult daily routine, with claim wording reviewed against EU regulation per market.

Use-case framing only. Specific on-pack claims must comply with EU 1924/2006 and the authorised list under EU 432/2012, and are reviewed per project.

Formula positioning

Mobility / bone range SKU. Collagen and minerals lead; format is chosen for taste compatibility.

Who this formula is for

A snapshot of the brand profiles that typically request calcium 600 + vitamin d3 tablet. Final fit is reviewed during the brief — your range, market and channel inform packaging, claim wording and certifications.

Mobility ranges
Bone-positioned brands
Teams needing formula + packaging + documentation support

Frequently asked questions

Can I request a sample before placing an order?
Yes. Sample requests go through the quote form. Lead time and sample format depend on packaging and any custom flavour or colour work.
What is the MOQ?
MOQ is confirmed per project. Standard white-label gummy MOQ starts at 1,000 units; doypack and fully custom configurations may carry a higher tier.
Which markets is this product suitable for?
Market eligibility depends on the labelling, claims and certifications required for your destination — reviewed per project against the relevant EU / UK / non-EU framework.
Do you provide a Certificate of Analysis?
A batch-specific Certificate of Analysis is provided after production and QC release. COA scope (microbiological, heavy metals, actives) is agreed up-front in the spec sheet.
Can the formula be customised?
Common adjustments include flavour, colour, sugar profile and packaging count. Active-ingredient changes are evaluated against EU food-supplement rules and may move the SKU into a custom-formula tier.
How long are typical lead times?
Lead time is confirmed in the quote. It depends on raw-material availability, packaging, artwork sign-off and the production calendar at the time of order.