Probiotics Gummy Manufacturer for Global Brands

Probiotics Gummy Manufacturer for Global Brands

EUPHM produces shelf-stable probiotic gummies in Guangdong, China. We run 1,000 unit MOQs, deliver samples in 7–10 working days, and hold GMP, ISO 22000 and HACCP certifications for US, EU, UK and Middle East buyers.

Probiotics Gummy Manufacturer for Global Brands

Overview

Sourcing a probiotics gummy manufacturer means balancing strain viability, pectin or gelatin texture, and retail shelf life. Our plant handles all three under one roof: probiotic blending, depositing, curing, and packaging. We work with brand owners, founders and procurement managers who need documented strain counts, clean-label options, and repeatable production runs. This page covers our capacity, formulation support, and compliance documentation so you can compare us against other gummy manufacturers.

Key specifications
MOQ (retail bottling)1,000 units per SKU
MOQ (pilot run)1,000 units per SKU
Sample lead time7–10 working days
Mass production20–35 working days after sample approval
Gummy fill weight2.5 g–5 g per piece
CertificationsGMP, ISO 9001, ISO 22000, HACCP, NSF/ANSI 455-2, halal, FDA-registered

Production Capacity for Probiotic Gummies

Our Guangdong facility runs two depositing lines dedicated to functional gummies. Each line produces 1.2–1.8 tonnes per shift, which translates to roughly 400,000–600,000 gummies per day at a 3 g fill weight. For probiotic gummies, we limit line speed to protect strain viability during the depositing and cooling stages. Typical annual output for probiotic SKUs sits between 80 and 120 million units, depending on bottle size and flavour changes.

We hold separate mixing rooms for probiotic blends to avoid cross-contact with non-live cultures. Temperature and humidity are logged every 15 minutes in the curing room, kept at 18–22°C and below 35% RH. If your brand needs a specific strain count at end of shelf life, we overage the formula and validate it with third-party testing at 0, 3, 6 and 12 months. This is standard practice for retail probiotic gummies in the US and EU.

Formulation and Strain Selection

We work with spore-forming strains such as Bacillus coagulans and Bacillus subtilis, which survive gummy processing better than many Lactobacillus or Bifidobacterium species. For brands set on Lactobacillus rhamnosus or Bifidobacterium lactis, we use a protective lipid or alginate coating and adjust the depositing temperature to 45–55°C. Typical inclusion rates are 1–5 billion CFU per gummy, with overage of 30–50% to meet label claims at end of shelf life.

Base options include pectin, gelatin, and tapioca starch. Pectin and tapioca suit vegan and halal claims; gelatin gives a firmer chew. We sweeten with cane sugar, tapioca syrup, allulose, or stevia. Flavours are natural or nature-identical, and we can match most commercial profiles. Colours come from fruit and vegetable concentrates if you want a clean label. Every formulation is locked after a 7–10 day sample round, and we provide a full ingredient breakdown for your regulatory review.

Quality Control and Shipping Logistics

Each batch is tested for total aerobic count, yeast and mould, and specific probiotic strain count at release. We also run water activity, hardness, and weight checks every 30 minutes on the line. Documentation includes a Certificate of Analysis, allergen statement, and GMO-free declaration. Our facility is FDA-registered and audited under GMP, ISO 22000 and HACCP. For halal or vegan claims, we maintain the relevant certificates and can share them during qualification.

Shipping from Shenzhen or Hong Kong ports takes 18–28 days to US West Coast, 22–30 days to EU ports, and 12–18 days to Jebel Ali. We pack in HDPE bottles with induction seals and desiccant where needed. Air freight is available for pilot runs. We handle FOB, CIF, and DDP terms. Lead times for mass production are 20–35 working days after sample approval, and we book production slots 3–4 weeks in advance for repeat orders.

Quality Control and Batch Documentation

Every probiotic gummy batch is assigned a batch number at the blending stage and tracked through depositing, curing, packaging and release. Incoming raw materials are checked for identity and documentation before use, including probiotic strain identity, carrier and pectin or gelatin grade. In-process checks cover deposit weight, piece count per tray, curing room temperature and humidity, and finished-piece texture. Release testing on the finished gummy covers total viable count, strain identity confirmation where declared, moisture content and water activity, heavy metals, and disintegration. Microbiological safety testing covers total plate count, yeast and mould, and specified pathogens per the destination market.

Potency testing is timed rather than done once. Because viable counts decline over shelf life, we test at release and again at defined intervals under the agreed stability protocol, typically at 0, 3, 6, 12 and 18 or 24 months depending on the declared shelf life. Overages are set so the label claim holds at end of shelf life rather than at release, and the overage figure is written into the specification you approve. Water activity is monitored closely because free moisture drives both viability loss and texture change.

The certificate of analysis issued with each batch states batch number, production date, expiry date, appearance, average piece weight, CFU count at release, moisture, water activity, heavy metals results against the agreed limit, microbiological results and disintegration time. It references the test methods used and the specification version. Where a customer needs strain-level confirmation, we can include the relevant method reference. A retained sample of every batch is held for the full shelf life plus six months, so any later query can be checked against the original material rather than a reconstruction.

Stability work follows a written protocol agreed before the first production run. Accelerated conditions are used to flag formulation risk early, while real-time data at ambient and, where relevant, tropical conditions supports the expiry date printed on pack. If a formulation changes, for example a swap from gelatin to pectin or a change in probiotic blend ratio, the stability clock restarts at the pilot stage. Documentation is retained and can be supplied to your quality team or to a contract laboratory acting on your behalf.

Packaging, Labelling and Retail Readiness

We fill probiotic gummies into HDPE or PET bottles with induction seals and desiccant where the formulation needs it, into blister packs, into single-serve stick packs, and into sachets for sample or travel formats. Bottle sizes typically run from 30 to 120 pieces. Desiccant and oxygen-scavenging options are chosen against the water activity and shelf life targets rather than by default. Child-resistant closures are available for markets that require them. Cartons are specified with board grade, print process and pallet pattern confirmed before mass production.

Label artwork is checked against the regulatory framework of the destination market. For the United States, that means the statement of identity, net quantity, supplement facts panel with serving size and percent daily values where applicable, other ingredients list, and the required address line for the distributor or manufacturer. Structure-function claims are reviewed so wording stays within permitted boundaries. For the EU and UK, the nutrition declaration, allergen emphasis and permitted claims list are checked separately, since the two frameworks have diverged.

Lot and expiry coding is applied at packing, with the format agreed per customer and per market. Typical formats are lot number plus best-before date in DD/MM/YYYY or MM/YYYY, inkjet or laser, on bottle base, label or carton as specified. We can apply Amazon FNSKU labels, poly-bag units, and retail-ready carton markings including ITF-14 barcodes where a retailer requires them. Carton specifications are confirmed with dimensions, gross weight and case count, and pallet configurations are set to the buyer's preferred height and pattern.

Before a retail launch we recommend a pre-production artwork proof and a physical pre-production sample in the final pack. This catches print colour drift, label placement on curved bottle surfaces, and seal integrity issues that flat artwork does not show. Where a retailer or marketplace has its own compliance checklist, we work through it with your team and record the outcome, so the first mass production run is not the first time the packaging meets the requirement.

MOQ, Lead Times and Delivery

The sampling stage typically takes 7 to 10 working days from approved formulation and artwork brief. That window covers pilot batching, depositing, curing and dispatch of the sample. If a new probiotic blend or a new flavour system is involved, add time for a second pilot round. Sample courier costs are quoted separately and are usually borne by the buyer. Sample quantities are normally 5 to 20 pieces per SKU, packed to reflect the intended retail format so texture and appearance can be assessed as the consumer would see them.

Mass production runs 20 to 35 working days after sample approval and receipt of deposit, depending on piece count, packaging format and whether custom tooling is needed. Curing time for pectin gummies is a fixed part of that window and cannot be compressed without affecting texture. We confirm a production slot at order confirmation and share a schedule with packing and dispatch dates. Changes to artwork or formulation after the slot is confirmed will move the dispatch date, so we ask for final sign-off before the slot is locked.

Shipping is arranged by air or sea depending on volume, destination and shelf-life sensitivity. Air freight suits smaller orders and time-critical launches; sea freight suits pallet volumes where the transit time fits the shelf life comfortably. We quote EXW, FOB and DDP. Under DDP the buyer receives a landed cost including duty and clearance, which simplifies budgeting, though the importer of record and local compliance obligations should be confirmed before ordering.

Documentation supplied with each shipment includes the certificate of analysis, safety data sheet where applicable, free-sale certificate, and commercial invoice and packing list. Certificates of origin can be issued on request. Where a destination requires phytosanitary or other specific certificates for the ingredients used, we confirm availability at quotation stage rather than after production. We also provide the product specification sheet and, where relevant, allergen and vegan statements, so your customs broker and regulatory team have a complete file before the container arrives.

Packaging and Format Choices

Vegan pectin base

Pectin and tapioca base for vegan, halal claims. No gelatin. Firmer bite than starch gummies. Works with spore-forming probiotics and coated Lactobacillus.

Spore-forming strains

Bacillus coagulans and Bacillus subtilis for high stability. No refrigeration needed. 1–5 billion CFU per gummy with 30–50% overage at end of shelf life.

Coated Lactobacillus

Lipid or alginate coating for Lactobacillus and Bifidobacterium. Protects strains during depositing at 45–55°C. Ideal for 1–2 billion CFU claims.

Sugar-free sweetening

Allulose, stevia or monk fruit instead of cane sugar. Reduces sugar to under 1 g per gummy. Suitable for keto and diabetic-friendly positioning.

From Enquiry to Delivery

  1. 01

    Brief and quote

    Send your strain, CFU target, base, flavour and bottle size. We reply with a quote and MOQ within 2 working days.

  2. 02

    Sample development

    We produce a 7–10 day sample round. You receive 50–100 gummies per flavour for sensory and stability review.

  3. 03

    Formulation lock

    After your feedback, we finalise the formula, overage percentage and label claim. You approve a signed specification sheet.

  4. 04

    Pilot run

    Optional 1,000–2,000 unit pilot run to confirm line settings, texture and packaging before full production.

  5. 05

    Mass production

    Full run of 1,000+ units per SKU. Production takes 20–35 working days. In-process checks every 30 minutes.

  6. 06

    QC and shipping

    Batch tested for strain count and microbiology. CoA issued. We ship FOB, CIF or DDP from Shenzhen or Hong Kong.

Why EUPHM

Strain viability focus

We overage formulas and test at 0, 3, 6 and 12 months. You get a documented CFU count at end of shelf life, not just at production.

Low MOQ for pilots

Start with 1,000 units per SKU. Scale to 1,000–2,000 for retail bottling. Lower risk for new probiotic gummy launches.

Full compliance pack

GMP, ISO 9001, ISO 22000, HACCP, NSF/ANSI 455-2 and halal certification; FDA facility registration for US-bound shipments.

Questions buyers ask.

What is the MOQ for probiotic gummies?+

Standard retail bottling starts at 1,000 units per SKU. Pilot runs can go as low as 1,000 units per SKU. MOQ depends on bottle size, flavour count and whether you need custom packaging. We confirm exact numbers in your quote within 2 working days.

How long do samples take?+

Sample lead time is 7–10 working days after we receive your brief and confirm the formula direction. You get 50–100 gummies per flavour for sensory review. We also provide a preliminary specification sheet with strain, CFU target and base type.

Can you match a specific CFU count at end of shelf life?+

Yes. We overage the probiotic inclusion by 30–50% and validate with third-party testing at 0, 3, 6 and 12 months. Common targets are 1–5 billion CFU per gummy. We document the result in the Certificate of Analysis for each batch.

Which certifications do you hold?+

Our facility holds GMP, ISO 22000 and HACCP. We also maintain halal and vegan certificates where the formula and supply chain qualify. The plant is FDA-registered. We share all certificates during supplier qualification.

What is the production lead time for mass orders?+

Mass production takes 20–35 working days after sample approval. This covers blending, depositing, curing, QC and packing. We recommend booking production slots 3–4 weeks ahead for repeat orders. Shipping from Shenzhen or Hong Kong adds 12–30 days depending on destination.

Do you test every batch for CFU count at release, or only periodically?+

Every batch is tested for viable count at release, and the result is recorded on the certificate of analysis against the approved specification. Release testing also covers moisture, water activity, heavy metals and microbiological safety. Potency is then re-tested at intervals under the agreed stability protocol so the end-of-shelf-life claim is supported by data rather than assumed from the release figure.

Can you produce probiotic gummies that are both vegan and halal certified?+

Yes, where the formulation uses pectin rather than gelatin and the probiotic strains and carriers meet the certifying body's requirements. Certification is held on the facility and product basis, so the specific SKU is submitted for approval before the claim goes on pack. We confirm which certificates apply to your formulation at quotation stage, since strain carriers and release agents can affect eligibility.

What happens if a batch fails a release test?+

The batch is placed on hold and not packed for shipment. We investigate the cause, which may be a raw material issue, a curing deviation or a testing anomaly, and re-test where the method allows. If the batch cannot meet specification, it is not released. You are informed with the test data and the proposed corrective action before any replacement production is scheduled.

Have a product in mind?

Send us the brief and we will come back with a formulation direction, indicative price and a realistic lead time — usually within one working day.