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Private-label supplement manufacturing across the formats brand owners actually launch — United States

One manufacturing network, two commercial options, four documentation review steps — applied across gummies, soft chews, oral strips, capsules, softgels and adjacent formats. The brand owner remains the food business operator on pack.

DAT Supply private-label manufacturing
Manufacturing platform

One platform, taken seriously across formats. Depth of formulation, packaging and documentation review — not a marketplace of vendors.

DAT manufactures private-label supplements through a project-managed production workflow. Format is chosen against the brand brief — not the other way around.

The Launch Loop
  1. 1 Select
  2. 2 Review
  3. 3 Sample
  4. 4 Approve
  5. 5 Produce
  6. 6 Deliver
Formats

Multi-format manufacturing, reviewed end to end

Each format runs through the same four-step review model — brief, spec, artwork, release — so documentation, packaging and positioning stay aligned across the range.

  1. Gummies

    Pectin-based supplement gummies — the mature DAT Supply format. Used across daily wellness, beauty, sleep and kids ranges.

    Gummies manufacturing →

  2. Sachets

    Single-serving sachet format for powders, granulates or compact daily-routine concepts. Configuration confirmed per project.

    Sachets manufacturing →

  3. Functional jellies

    Pouchable functional jelly format for daily-routine and on-the-go supplement concepts.

    Functional jellies manufacturing →

  4. Oral strips

    Fast-dissolving oral strip format. Reviewed per project; payload range confirmed during the brief.

    Oral strips manufacturing →

  5. Patches

    Transdermal / topical supplement patch format. Active suitability and skin-adhesive compatibility are reviewed per project — feasibility is confirmed before any spec lock, and DAT publishes no transdermal absorption or therapeutic claims.

    Patches manufacturing →

  6. Pet supplements

    Soft chews and adjacent formats for dog and cat wellness ranges, reviewed per species claim framework.

    Pet supplement manufacturing →

Options

Pick the option that matches the brief.

Every project moves through one of two options. Final routing is confirmed inside the portal — the option shapes the documentation set and the timeline.

Brief inputs

What DAT needs before reviewing manufacturing

The inputs below shape the route, the format, the documentation set and the project timeline.

  1. 01
    Target market

    Primary distribution market and any secondary markets — drives label, claims and notification scope.

  2. 02
    Quantity

    Indicative MOQ tier and forecast for the launch window. Used to confirm route and packaging.

  3. 03
    Formula direction

    Positioning, active ingredients in scope and any non-starters. Custom development is reviewed against the brief.

  4. 04
    Packaging format

    PET bottle, doypack or sachet — pack format influences the production route and documentation set.

  5. 05
    Timeline

    Target launch window. Production calendar and raw-material lead times are confirmed during order setup.

  6. 06
    Claims & label requirements

    Any approved claim wording, regulatory framework, or label requirement you already need to honour.

Manufacturing operations

DAT manages the project end to end

DAT manages supplement launches from formula selection through production, documentation review and batch release. Project-specific documentation and facility details are handled inside the project workflow where required — released to the brand owner per project stage, not as a public list.

  • Controlled manufacturing route, confirmed per project
  • Project-stage documentation; batch-specific QC release
  • Target-market review for claims, labelling and notifications
US brands

Manufacturing support for US brands — by state

DAT Supply coordinates private-label manufacturing for US brand owners across all 50 states. Production runs through the controlled manufacturing workflow, with documentation reviewed remotely.

See manufacturing support by US state →

Project handoff

Start an order

Send your order brief — DAT will review and route it to the right working track. Final routing is confirmed inside the portal once the brief has been reviewed.

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. Order documents, certificates and pricing are released through the client workspace in the DAT portal.

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