- Private-label formula ready for your brand
- Order samples before production
- Choose PET bottle, doypack or gummy sachet during order setup
- Documents and approvals managed in your DAT Supply account
- 1 Select
- 2 Review
- 3 Sample
- 4 Approve
- 5 Produce
- 6 Deliver
Product overview
The reviewed private-label concept, framed for brand owners.
Electrolyte 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.
Sample Electrolyte Gummies before you commit
Order a sample of this product to review texture, flavour and finish — the expected next step before a production run. No account needed to start.
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.
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?
Minimum order quantities for Electrolyte Gummies are published, not quoted: from 1,000 units in PET bottle, 2,500 units in doypack and 1,000 units in gummy sachet. A custom formula is a separate lane: production is generally from 10,000 units; exact MOQ is confirmed during feasibility and depends on product format, formulation and ingredient sourcing.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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