A focused private-label supplement manufacturing partner for serious brands.
DAT Supply runs a controlled manufacturing route for private-label supplements across multiple formats. We do not run a marketplace and we do not sell to consumers — the brand owner remains the food business operator on pack.
- Reviewed concepts
- 212+
- Working routes
- 3
- Project gates
- 4
- Pathways
- EU · UK · US
DAT Supply manages supplement launches end to end — formula selection, production, documentation review and batch release. The brand owner stays on pack.
A focused B2B private-label supplement manufacturing partner for serious brands.
What makes DAT different
Five operating choices that shape every project — restated as a discipline, not a list of features.
- 01
One product category
Private-label supplements. We focus on a defined set of formats — gummies, capsules, softgels, chews and adjacent — instead of stretching across every category. The catalogue is smaller, the depth is higher.
- 02
B2B only
DAT is a manufacturing partner for brand owners and operators. We do not sell to consumers and we do not run our own DTC ranges that would compete with our clients.
- 03
Documentation by project stage
Specification, label review, batch documents and packaging documents each move through their own gate. The Certificate of Analysis is batch-specific and post-production.
- 04
Controlled formulation and packaging routes
White-label, semi-custom and custom routes. Format (PET bottle, doypack, sachet) is independent from positioning — the brief is reviewed against both axes before specification.
- 05
Compliance-aware, not a regulatory agency
On-pack claim wording is reviewed against the relevant target-market framework as part of each project. The brand owner remains the food business operator and is responsible for final filings.
Private-label supplements across the formats brands actually launch.
Manufactured formats include gummies, capsules, softgels, soft chews, oral strips, powders, shot vials, drops and adjacent. Vegan-positioned formats are available subject to formula and target-market review. Gelatin and halal positioning are available on request and are subject to project-specific review and certification scope — not a default.
Packaging routes include PET bottle, doypack and sachet. Pack configuration is confirmed per project — including units per sachet, sachets per outer, film, outer packaging and logistics.
Beauty & Skin, Energy & Focus, Daily Wellness, Sleep & Mood, Digestive & Gut, Kids & Family, Women's / Men's Health, Joint & Bone, Immune Support and Botanicals & Mushrooms — all reviewed independently of format so the same concept can move between packaging types without changing the brief.
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.
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Formula selection
White-label, semi-custom or custom — confirmed against the brief.
-
Production through a controlled workflow
Private-label supplement production runs through DAT's controlled manufacturing workflow across every supported format.
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Documentation by project gate
Specification, label, packaging and batch-release each move through their own gate.
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Batch release after QC
Batch-release documents are issued after production and QC release.
A clean path from brief to released batch.
The brief, the formula, the documentation route and the batch release each move through their own gate.
- 01
Brief
Target market, format, quantity, claims direction, timeline.
- 02
Route
White-label, semi-custom or custom — confirmed against the brief.
- 03
Specify
Per-SKU specification + allergen statement drafted, then locked.
- 04
Artwork
Dieline, on-pack copy and claim wording reviewed per market.
- 05
Produce
In-process control plan agreed; production runs through the controlled network.
- 06
Release
Batch-specific COA after QC release; documentation refreshed per stage.
What gets reviewed, when, and what the brand owner receives
DAT releases documentation as the project moves through each gate. Batch-release documents are issued after production and QC release.
- 01StageBrief reviewReviewed
Target market, format, quantity, claims direction
WhenProject entry
ReceivesFeasibility view + working route confirmation
- 02StageFormula & spec confirmationReviewed
Formulation route, allergen statement, per-SKU specification
WhenAfter brief sign-off
ReceivesSpecification draft + spec-locked formula
- 03StageArtwork & label reviewReviewed
Dieline, on-pack copy, claim wording per market framework
WhenIn parallel with spec lock
ReceivesReviewed artwork against the target-market framework
- 04StageProduction & batch releaseReviewed
In-process control plan, QC release rules, per-batch traceability
WhenOnce spec & artwork are signed off
ReceivesProduction run + batch-specific Certificate of Analysis
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.
Working on a supplement launch?
Pick the working route inside the DAT portal — white-label, semi-custom or custom. The wizard takes the brief and routes it through the right project gate.