Skip to content
DAT Supply Log in
Manufacturing / Gummies

Private-label gummy manufacturing for brands that want to launch confidently.

Pectin-based gummy supplements with three working routes, four documentation gates and packaging confirmed per project. The brand owner stays the food business operator on pack.

Base
Pectin
Working routes
White-label · Semi-custom · Custom
Documentation
4 gates by project stage
Private-label gummy manufacturing for brands that want to launch confidently. — DAT Supply manufacturing
Working routes
3

white-label · semi-custom · custom.

Project gates
4

brief · spec · artwork · release.

Pathways
EU · UK · US

reviewed per target-market framework.

Format manifest

Pectin gummies are DAT's deepest format. Formulation, packaging and documentation are reviewed end to end — not split across vendors.

Gummies at a glance
Base
Pectin
Formats
PET · Doypack · Sachet
Routes
White-label · Semi-custom · Custom
Pathways
EU · UK · US
Best-fit use cases

When gummies are the right format

Gummies fit ranges that need broad consumer appeal, a familiar daily ritual, and a packaging story that reads on shelf and online. Below are the launch shapes we see most often.

Launch routes

Pick the route that matches the brief.

Every project moves through one of three routes. Final routing is confirmed inside the portal — the route shapes the documentation set and the timeline.

Packaging options

PET bottle · Doypack · Sachet

Format is independent from positioning. The same formula concept can move across packaging types — DAT confirms the right fit during the brief.

  1. PET bottle

    Canonical supplement-shelf format. Suits 30/60-day daily-use ranges with a clear nutrition table.

  2. Doypack

    Stand-up pouch with resealable zip. Strong DTC unboxing and lower secondary-packaging footprint.

  3. Sachet

    Single-serve daily ritual or travel SKU. Sachet configuration (gummies per sachet, film, outer) is confirmed per project.

Documentation route

Project gates, not promises

DAT releases documentation as the project moves through each gate. Batch-release documents are issued after production and QC release.

  1. 01
    Stage
    Brief review
    Reviewed

    Target market, format, quantity, claims direction

    When

    Project entry

    Receives

    Feasibility view + working route confirmation

  2. 02
    Stage
    Formula & spec confirmation
    Reviewed

    Formulation route, allergen statement, per-SKU specification

    When

    After brief sign-off

    Receives

    Specification draft + spec-locked formula

  3. 03
    Stage
    Artwork & label review
    Reviewed

    Dieline, on-pack copy, claim wording per market framework

    When

    In parallel with spec lock

    Receives

    Reviewed artwork against the target-market framework

  4. 04
    Stage
    Production & QC
    Reviewed

    In-process control plan, stability and QC release rules

    When

    Once spec & artwork are signed off

    Receives

    Production run + in-process control records

  5. 05
    Stage
    Batch-specific documents
    Reviewed

    Per-batch QC, traceability, release-for-shipment

    When

    After production & QC release

    Receives

    Batch-specific Certificate of Analysis + traceability

  6. 06
    Stage
    Repeat order support
    Reviewed

    Forecast review, raw-material lead times, improvement notes

    When

    Per repeat order

    Receives

    Refreshed documentation per project stage

Documentation availability depends on product, market and project stage. The brand owner remains the food business operator and is responsible for final filings in each target market.

Related product concepts

Concepts reviewed for this format

A short pick of reviewed concepts. Final positioning, claims and documentation are reviewed per project.

Explore the full product catalogue →

Related ingredients

Common actives for this format

Frequently asked questions

  • What base do DAT gummies use?

    Pectin. The platform is pectin-first across PET bottle, doypack and sachet formats. Gelatin is out of scope.

  • Which formats can the same gummy concept ship in?

    A reviewed gummy concept can move across PET bottle, doypack or sachet packaging. DAT confirms the right fit during the brief.

  • How are projects routed?

    White-label adapts a reviewed concept and brand artwork. Semi-custom adjusts dose, flavour or active stack within an existing matrix. Custom development covers bespoke formulation and packaging.

  • What documentation does DAT release at each project stage?

    Four gates: brief review, spec confirmation, artwork review per the target-market framework, and batch-specific Certificate of Analysis after QC release. The brand owner remains the food business operator on pack.

  • Can DAT support multi-market EU + UK + US launches?

    Yes — every project is reviewed against the target-market framework (EU FIC, UK FSA, US DSHEA) so the same formulation can move across pathways with the right documentation pack.

  • What is the order of magnitude for a first gummy run?

    White-label projects start from 1,000 units (PET bottle). Semi-custom starts from 2,500 units (doypack). Custom development starts from 5,000 units. Final volumes are confirmed in the quote.

Project handoff

Start a gummy project

Send your gummy brief — DAT will review and confirm the working route, packaging fit and documentation set inside the project workflow.

Quick context request

Get manufacturing context

Drop your work email and a member of the DAT team will follow up with the right context for this concept. Project documents, certificates and pricing are released through the project workspace in the DAT portal.

You will receive a short confirmation email. Project documents (specification, batch-specific COA, packaging documents) are released through the project workspace in the DAT portal once a brief is in place.