Skip to content
DAT Supply Log in
Pet Supplements / Pastes

Pet pastes — syringe-applied formats for high-active pet ranges.

Paste formats applied via syringe. Texture, active load and palatability are reviewed per species before spec lock.

Species
Dog · Cat · Horse
Routes
Custom
Gates
Brief · Spec · Artwork · Release
Pet pastes — syringe-applied formats for high-active pet ranges. — 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

Pet pastes are reviewed per feasibility and per species framework.

Pet pastes at a glance
Species
Dog · Cat · Horse
Format
Syringe-applied paste
Routes
Custom
Gates
Brief · Spec · Artwork · Release
Best-fit use cases

When a pet paste fits

Pastes suit ranges that need a high active load in a small volume — joint stacks, recovery stacks, performance stacks.

Manufacturing capability

How pet pastes are made

Pet pastes are concentrated active deliveries applied via syringe or squeeze tube, designed to carry a high active load in a small volume tolerated by dogs, cats and equine species. The base layers oil systems, glycerin, malt syrups and palatability enhancers (liver paste, hydrolysed protein, molasses for equine) over the active stack. Payload is the platform advantage — joint-support stacks with glucosamine, chondroitin and MSM at full clinical doses, recovery stacks built around branched-chain amino acids and electrolytes for working dogs and equine athletes, gut-stack pastes layering prebiotics, probiotics and digestive enzymes, and immune-support pastes for transitional life stages (puppies, kittens, post-illness recovery). Texture is tuned to the dosing format — a syringe paste flows under thumb pressure but holds shape on the tongue; a tube paste extrudes cleanly and resists separation. Standard finish options include species-specific flavour systems, dose-graduated syringe markings, and tube-end clips for partial-dose retention. Brands choose pastes when daily compliance compresses (a 5-second hand-dose beats a 30-minute chew-search), when the active load needs to be high in a small volume, or when the format is the standard in the channel (equine pastes are the dominant horse-supplement format).

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.

Working routes in detail

What each route looks like for pastes

White-label

White-label availability is reviewed per project. Paste chemistry and dosing hardware sit inside the spec. DAT confirms in the brief.

Semi-custom

Semi-custom is reviewed where a published paste matrix can be adjusted for flavour, dose graduation or pack format. First runs land at the 2,500-unit MOQ tier where the matrix supports the change; DAT confirms before spec lock.

Custom

Custom is the dominant pet-paste route — bespoke actives, premium emulsions, species-specific dosing hardware and bespoke outer presentation. First runs land at the 5,000-unit MOQ tier and timelines are confirmed per project.

Packaging options

Syringe · Tube

Hardware is confirmed per project — syringe, dose graduation and outer carton reviewed during brief.

Pet-paste packaging is reviewed against the dose ritual and channel. Dose-graduated syringes are canonical for hand-dosed daily-use SKUs and equine athletes; the syringe length, graduation interval and plunger lock are tuned to species and dose. Squeeze tubes (75-200 mL) suit multi-dose family routines and clinic-channel SKUs. Across all formats, the outer carton, dose chart, species framework on pack and tamper evidence are confirmed in the brief.

  1. Syringe

    Premium dose-graduated format.

  2. Tube

    Cost-efficient multi-dose format.

Packaging considerations
  • Dose-graduated syringe
  • Plunger-lock syringe
  • Squeeze tube (75-200 mL)
  • Tube-end clip / cap
  • On-pack species framework
  • Dose-chart insert
  • Outer carton or shipper
  • Tamper-evident seal
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 →

Reviewed ingredients

Top ingredients reviewed in pastes

Ingredients commonly reviewed for this format in the DAT Supply dossier library. Open a dossier to see dose anchors, working forms and per-format formulation considerations.

Browse all reviewed ingredients →

Related ingredients

Common actives for this format

Regulatory framework

EU, UK and US documentation for pet pastes

Pet pastes are placed as complementary feed under Regulation (EC) 767/2009 with FEDIAF guidelines in the EU; UK retained law mirrors this. Equine pastes route via the same framework with horse-specific FEDIAF guidance. US launches route via the FDA / AAFCO food-for-pets framework or NASC-aligned animal health where applicable. DAT releases brief, spec, artwork and batch CoA documentation aligned to the chosen pathway and target species.

Frequently asked questions

  • Is white-label available for pet pastes?

    Pet pastes typically route through custom because paste chemistry and dosing hardware are bespoke per project. White-label availability is confirmed per project against the reviewed catalogue.

  • What documentation gates apply?

    Brief review, spec confirmation, artwork review per the target-market and species framework, and batch-specific Certificate of Analysis after QC release.

  • Does DAT review equine paste SKUs?

    Yes — equine pastes are routinely reviewed against horse-specific FEDIAF guidance, with dose-graduated syringes and palatability systems tuned to the horse market.

  • How is dose calibration handled on a syringe paste?

    Dose-graduated syringes carry markings tuned to body weight or per-day dose; the graduation interval, plunger lock and on-pack dose chart are confirmed in the brief.

  • Can a paste be partial-dosed across multiple days?

    Yes — syringes carry a plunger lock or end clip for partial-dose retention, and tube formats hold their seal across multi-dose use. Shelf stability after first use is confirmed per project.

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

    Custom development starts from 5,000 units. Final volumes are confirmed in the quote after brief review.

Project handoff

Request a pet paste quote

Send the brief — DAT will review feasibility and frame the spec lock.

Reviewed concepts

Reviewed pet pastes concepts

Public-ready PIM concepts detected as pet pastes. Each entry is a starting point — species fit, palatability and packaging are confirmed per project. DAT does not publish pet therapeutic claims.

View the combined pet catalogue →

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.