Magnesium Citrate Gummies
Private label magnesium citrate gummies for supplement brands.
- 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.
Product overview
The reviewed private-label concept, framed for brand owners.
Magnesium Citrate 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 mineral name over a confirmed B6 formula
Magnesium Citrate Gummies carries a mineral-form name, but the catalogue's confirmed formula record lists a single active: pyridoxine hydrochloride, the hydrochloride salt form of Vitamin B6. B6 is a common cofactor pairing on magnesium-positioned SKUs elsewhere in the catalogue, so its presence here is consistent with that pattern, but the record does not itself carry a magnesium line. The name is this product's magnesium signal, and the confirmed active is the B6 cofactor rather than the mineral itself, a distinction a brand should carry through to its own pack copy rather than smoothing over.
That gap is worth stating plainly to a brand evaluating this SKU: pack copy built only from the confirmed record should describe a B6-formulated gummy inside the catalogue's magnesium-positioned family, and any magnesium content claimed on a label should be checked against the underlying formulation sheet during order setup rather than assumed from the product name alone. The gummy format itself follows the catalogue's standard pectin-based, target-market reviewed build shared across the range, so the formulation gap, not the manufacturing process, is the detail worth flagging early.
A targeted addition next to a fuller daily line
Daily Vitamins is the catalogue's foundational range for brands building a general daily-coverage multivitamin line, and a mineral-named single-active gummy like this one typically sits as a targeted addition next to a fuller multivitamin SKU rather than replacing it, the kind of concept a brand adds once its core daily line is already listed and selling well on its own shelf. It is a secondary listing, not a range-opening one, in most private-label catalogues built this way, added once a brand has an existing customer base to cross-sell a narrower concept to.
Zinc Magnesium B6 Gummies is the closest confirmed sibling in the same category, sharing the identical pyridoxine hydrochloride active on its own record, which makes the two SKUs a useful side-by-side for a brand deciding whether to list a single mineral-name concept or a combined mineral-and-B6 one built from the same confirmed active base, before either formulation record is expanded further with additional minerals as the range matures and shopper feedback comes in. A brand's own catalogue plan, not this comparison alone, should decide exactly how the SKU sits alongside its neighbours on shelf.
Personalising and ordering the confirmed formula
Make it Yours covers approved flavour, colour and shape on the confirmed formula. Because the record carries one active, pack presentation and the accuracy of any on-label ingredient claim carry more of the differentiation weight than a busier, multi-active formula would need to lean on, particularly given the gap between the product's own name and its verified formulation content that a brand should carry into its own artwork review before print approval. A brand should raise any pack-presentation preference at this stage rather than after artwork is already underway and harder to change.
Adding a confirmed magnesium line, changing the B6 dose, or introducing a new mineral claim moves the project into the separately scoped Custom Product R&D route instead. Sampling the confirmed formula comes first, and label claims plus market compliance, including verifying any magnesium claim against the true formulation sheet, remain the brand owner's responsibility throughout the process, well ahead of any market launch or retailer submission in a new territory. Any packaging preference sits alongside this same personalisation step, reviewed together before a sample run is confirmed.
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.
- Vitamin B6 (Pyridoxine) 1.4 mg
Sample Magnesium Citrate 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 Magnesium Citrate 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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