- Private-label formula ready for your brand
- Order samples before production
- Choose PET bottle or doypack during order setup
- Documents and approvals managed in the portal
- 1 Select
- 2 Review
- 3 Sample
- 4 Approve
- 5 Produce
- 6 Deliver
Packaging and minimum order quantities
Confirmed against your brief during order setup — after you have seen samples, never before. Project-specific packaging, flavour, colour or shape adjustments may be reviewed after order start.
The standard PET jar route for a first production run.
Stand-up pouch packaging on the same private-label route.
Single-serving sachet — gummies portioned for daily-routine and travel.
Pricing confirmed on request — Request a quote.
Product overview
The reviewed private-label concept, framed for brand owners.
Vitamin D3 + K2 Gummies is a private-label gummy SKU available for private-label brand launches. manufactured to specification under EU food supplement directives. Pectin-based formulation by default. Standard MOQ is 1000 units (HDPE jar) or 2500 units (doypack). Custom packaging and formulation development available subject to MOQ tier. Documentation pack included for the target market's notification regime.
A fat-soluble compound moved from softgel to gummy
Vitamin D3 + K2 Gummies tracks one active on its formula table: menaquinone-7, a specific compound within the vitamin K2 family, named by its exact chemical form rather than a general category label.
Fat-soluble compounds like this one are conventionally sold in an oil-filled softgel, since the fat-soluble structure pairs naturally with an oil-based capsule shell. Carrying menaquinone-7 in a pectin gummy instead is a format shift away from that convention — the same compound class delivered as a chew rather than a swallowed capsule, and one tracked line doing that work rather than a multi-active panel.
A compound-specific entry on the Daily Vitamins shelf
The registry files this under Daily Vitamins, the grouping built around a foundational, daily-coverage multivitamin range that most brands treat as their opening SKU before adding narrower, more targeted concepts.
Naming the exact compound, menaquinone-7, rather than a broader vitamin category gives a brand a more specific ingredient story to put on pack than a generically labelled entry would, which can matter for a range that wants to differentiate its Daily Vitamins line on formulation detail rather than on range breadth alone. That same specificity gives a brand's own technical and label copy a single, unambiguous compound name to build from rather than a broader, less precise class term.
Personalising the menaquinone-7 gummy formula
Make it Yours covers approved flavour, colour and shape on this exact formula, with the menaquinone-7 content held fixed inside that route. Moving a fat-soluble compound into a gummy format already changes texture and delivery from the category's more common softgel format, so flavour and colour are the remaining levers a brand controls without touching that underlying choice.
A second active, a different amount, or a new claim is out of scope for Make it Yours and instead routes to Custom Formula R&D. This exact formula samples first, with the brand owner responsible for claims and market-compliance review from there.
Active ingredients
The actives in the current standard formulation. Final formula is reviewed and locked against the project brief.
Per-serving dose; % Daily Value (DV) shown for applicable nutrients per FDA 21 CFR 101.36. Values reflect the current standard formulation and are locked at specification stage.
- Menaquinone-7 0.1 mg
Sample Vitamin D3 + K2 Gummies before you commit
Order a sample kit from your client workspace to review texture, flavour and finish — the expected next step before a production run.
Documents managed by order stage (US market)
Each document is released into your client workspace as the order moves through its review stages — never a public download. DAT releases the standard documentation package by project stage. External testing, full COA, additional microbiological reports, heavy metals, pesticide residue reports or raw-material supplier documentation are reviewed and quoted separately unless included in the agreed project scope.
- Product specificationOrder gate
Drafted at brief stage; locked before production. FDA/US market compliance confirmed.
- Nutrition / supplement factsOrder gate
Per-serving values and the US Supplement Facts label (21 CFR 101.36). Prepared per target market and DSHEA framework.
- Artwork checklistOrder gate
Dieline, on-pack copy and structure-function statement wording reviewed against DSHEA (21 USC §343(r)(6)) compliance.
- Batch / release documentsOrder gate
Issued after production and QC release — always batch-scoped. subject to per-market regulatory review testing summary available on request per project scope.
- Compliance dossierOrder gate
Supporting documentation (DSHEA structure-function substantiation, ingredient sourcing, FDA compliance evidence per project scope).
- Certificate of AnalysisOrder gate
A batch-specific Certificate of Analysis is available on request after production — ingredient identity, potency and contaminant screening.
Documentation availability depends on product, target market and project stage. The brand owner remains the food business operator and is responsible for final filings.
Where this concept sits
Where this concept slots into a brand plan. Positioning and claims are reviewed per project and target market.
Brand range expansion
Slot Vitamin D3 + K2 Gummies into an existing supplement range as the gummy 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 target-market regulations per market.
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. Ready private-label option starts at 1,000 units in PET jars and 2,500 units in doypacks; custom configurations are confirmed after scope.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 typically 8–12 weeks depending on format, packaging, production slot and destination. Final timeline is confirmed during order setup before payment.
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