
Multivitamin Softgel Manufacturer for Global Brands
EUPHM produces multivitamin softgels in a GMP-certified facility in Guangdong, China. We handle formulation, encapsulation, and packaging for brands in the US, EU, UK, and Middle East. MOQ starts at 1,000 units per SKU.
Overview
Sourcing a reliable multivitamin softgel manufacturer means balancing formulation complexity, fill weight accuracy, and regulatory compliance. EUPHM operates a dedicated softgel line with a 1.2 million softgel daily capacity. We work with brand owners and procurement managers who need consistent potency, clean labels, and predictable lead times. Our team supports pilot runs as low as 1,000 units and scales to full retail bottling without reformulation. Certifications include GMP, ISO 22000, HACCP, and halal options where required.

Softgel Capability and Line Capacity
Our softgel line runs rotary die encapsulation with a fill weight range of 150 mg to 1,200 mg per softgel. We handle both oil-based and suspension fills. Typical multivitamin softgels use a gelatin or vegetarian shell. For vegetarian options, we use modified starch or carrageenan. Changeover between SKUs takes 4–6 hours. This supports small pilot runs without long downtime.
We run 24-hour operations, five days a week. That gives a monthly output of approximately 26 million softgels. Bottling lines handle 30, 60, 90, 120, and 180 count sizes. We also offer blister packing and pouch filling. In-process checks occur every 30 minutes for fill weight, shell thickness, and seam integrity. This keeps rejection rates below 1.5 percent.
Multivitamin Formulation and Ingredient Options
Multivitamin softgels typically combine fat-soluble vitamins (A, D, E, K) with water-soluble vitamins (B-complex, C) in an oil suspension. We source vitamin premixes from suppliers with USP or EP grade documentation. For oxidation-sensitive ingredients like vitamin A and D, we use nitrogen flushing during encapsulation. This extends shelf life to 24 months in a sealed bottle.
You can choose from standard RDA-level formulas or high-potency blends. Common requests include 800 mcg folic acid, 50 mcg vitamin D3, and 100 mg vitamin C per softgel. We also add minerals like zinc and selenium as chelated forms. For vegan softgels, we replace gelatin with tapioca starch. Organic options require certified ingredients and a dedicated production window.
Quality Control and Compliance Documentation
Every batch undergoes identity testing for incoming raw materials via HPLC and GC. Finished softgels are tested for potency, disintegration, and microbial safety. We retain samples for 24 months. Our facility is FDA-registered and follows 21 CFR Part 111. For EU clients, we provide documentation for EFSA compliance. For UK clients, we align with UKCA requirements.
Halal certifications are available on request. Organic production runs require a 24-hour cleaning window and separate documentation. We issue a Certificate of Analysis (CoA) for each batch. We also provide MSDS, allergen statements, and country-of-origin declarations. Third-party lab testing can be arranged at cost. Lead time for documentation is 3–5 working days after production.
Packaging, Labelling and Retail Readiness
Multivitamin softgels can be packed in HDPE bottles, blister packs, stick packs or sachets. Bottle options include 30, 60, 90, 120 and 180 count, with induction seals and child-resistant or standard screw caps. Blister packs use PVC/PVDC or aluminium cold-form foil for moisture-sensitive formulations. Stick packs and sachets are typically 5–10 g and suit single-dose or travel formats. We can apply desiccant canisters or silica gel sachets inside bottles where the formulation requires low humidity. Bottle labelling supports up to four panels with a maximum label height of 120 mm, and we can print lot and expiry codes by inkjet or laser on the bottle, label or carton as specified.
For the US market, labels must include the Supplement Facts panel with serving size, amount per serving and % Daily Value for each active, plus the complete ingredient list in descending order of predominance. Allergen declarations are required under FALCPA for milk, eggs, fish, crustacean shellfish, tree nuts, peanuts, wheat and soybeans. The label must also show the net quantity of contents, name and place of business of the manufacturer or distributor, and a domestic address or phone number for reporting serious adverse events. We review artwork against these elements before printing and will flag missing items, but final label compliance remains the brand owner's responsibility.
Cartons are specified to withstand retail distribution. A typical shipper holds 24 or 48 bottles, with dimensions and gross weight confirmed per SKU. Pallet configurations are designed for standard 1200 x 1000 mm or 1200 x 800 mm pallets, with stretch wrapping and edge protectors. For Amazon FBA, we can print and apply FNSKU labels, poly-bag units where required, and apply suffocation warning labels. Carton weight and dimension data can be supplied in the format required for the seller central shipment plan. We do not apply retail price stickers unless supplied by the buyer.
Lot and expiry coding follows the buyer's format, typically Julian date or YYMMDD, with the expiry date calculated from the stability data supporting the declared shelf life. We retain a packaging record for each batch that includes label version, artwork approval date and code verification. If a label revision occurs mid-production, the change is controlled by a documented change order and the affected batches are identified. Retailer-specific requirements such as Target's or Walmart's carton marking can be accommodated if the specification is provided before production.
MOQ, Lead Times and Delivery
Sample production for a new multivitamin softgel formulation takes 7–10 working days after formula and shell specification approval. This includes pilot encapsulation, in-house testing and dispatch of samples by courier. If custom packaging is required, add 5–7 working days for label printing and bottle sourcing. Sample costs are quoted per project and are typically credited against the first mass production order. We recommend approving the sample against a written specification that lists actives, fill weight, softgel dimensions, shell composition and packaging, so that mass production matches what was tested.
Mass production lead time is 20–35 working days from receipt of purchase order, deposit and approved artwork. This window covers raw material procurement, encapsulation, drying, QC release, packaging and final inspection. Delays occur most often when artwork approval or deposit payment is late, or when a vitamin source requires a new supplier qualification. We provide a production schedule at order confirmation and update it weekly. For repeat orders with unchanged specifications, lead time is typically at the lower end of the range.
Shipping is by air or sea depending on volume and urgency. Air freight from Guangdong to Europe or North America typically takes 5–10 days door to door, while sea freight takes 25–40 days port to port plus customs clearance. We quote EXW, FOB Shenzhen or Hong Kong, and DDP for selected destinations. DDP pricing includes freight, insurance, duties and customs clearance, but the buyer remains responsible for product compliance in the destination market. For sea shipments, we provide a packing list with carton dimensions, net and gross weight, and pallet count.
Documentation provided with each shipment includes the commercial invoice, packing list, bill of lading or air waybill, Certificate of Analysis for each batch, and a Material Safety Data Sheet where applicable. A free-sale certificate can be issued for markets that require it, and phytosanitary certificates are provided for botanical-containing formulations when the destination country requests them. Certificates of origin can be arranged for preferential tariff treatment under applicable trade agreements. We do not provide import licences or product registrations, which remain the buyer's responsibility.
Options for Your Format
Gelatin shell
Standard bovine or porcine gelatin. Suitable for most multivitamin oil suspensions. Provides 24-month shelf life. Not for vegetarian or vegan labels.
Vegetarian shell
Modified starch or carrageenan. Vegan-friendly. Slightly lower oxygen barrier than gelatin. Recommended for plant-based multivitamins.
Enteric coating
Delayed release for sensitive ingredients. Reduces stomach upset from high-dose vitamins. Adds 2–3 days to production lead time.
Custom fill weight
From 150 mg to 1,200 mg per softgel. We adjust fill weight to match your label claim. Tolerance is ±5 percent.
Production in Six Steps
- 01
Inquiry and quotation
Send your formula, target fill weight, and bottle count. We reply within 1 working day with pricing and MOQ confirmation.
- 02
Sample production
We produce 100–200 sample softgels. Lead time is 7–10 working days. You approve fill weight, shell, and appearance.
- 03
Purchase order
Confirm PO with 50 percent deposit. We lock in raw materials and schedule your production window.
- 04
Mass production
Production runs 20–35 working days. You receive in-process updates every 5 working days, including fill weight logs.
- 05
Quality testing
Finished batches undergo potency, disintegration, and microbial testing. CoA is issued within 3 working days.
- 06
Packaging and shipping
Bottling, labelling, and packing take 5–7 days. We ship FOB Shenzhen or arrange air freight. Delivery to US/EU takes 15–25 days.
Why EUPHM
Low MOQ for pilots
Start with 1,000 units for pilot runs. Scale to 1,000 units for retail bottling without reformulation.
Full certification stack
GMP, ISO 9001, ISO 22000, HACCP, NSF/ANSI 455-2 and halal certification; FDA facility registration for US-bound shipments.
Transparent lead times
7–10 days for samples. 20–35 days for mass production. Realistic timelines, not optimistic promises.
Questions buyers ask.
What is the MOQ for multivitamin softgels?+
MOQ is 1,000 units per SKU for retail bottling. For pilot runs, we accept 1,000 units. This lets you test the market before committing to full production. No reformulation is needed when scaling up.
Can you produce vegetarian or vegan multivitamin softgels?+
Yes. We use modified starch or carrageenan shells instead of gelatin. Vegan certification is available. Note that vegetarian shells have a slightly lower oxygen barrier than gelatin. We recommend nitrogen flushing for oxidation-sensitive vitamins.
What certifications does your facility hold?+
We hold GMP, ISO 22000, and HACCP. Halal, and vegan certifications are available on request. Our facility is FDA-registered. We provide all documentation for EU, UK, and Middle East regulatory submissions.
How long does sample production take?+
Sample lead time is 7–10 working days after formula approval. You receive 100–200 softgels for evaluation. We include a preliminary CoA for fill weight and appearance. Courier delivery to US or EU takes 3–5 days.
What is the shelf life of your multivitamin softgels?+
Shelf life is 24 months when stored in a sealed bottle below 25°C and 60% relative humidity. We use nitrogen flushing for oxygen-sensitive ingredients. Accelerated stability testing is available at additional cost. Real-time stability data can be provided for existing formulas.
Can you match a competitor's multivitamin softgel formula?+
We can develop a formula to match a supplied specification or reference product, but we do not copy a competitor's proprietary formula without confirmation that you have the right to use it. Send the actives, target potencies, fill weight and any claims, and our formulation team will propose a softgel composition and shell system. Reverse engineering from a label is possible for many vitamin profiles, but exact match of excipients and shell requires a sample for comparative analysis.
What is the shelf life of your multivitamin softgels and how is it supported?+
Shelf life is typically 24 months when stored below 25°C in a dry place, but the final declaration depends on the formulation and packaging. We support the shelf life with ICH Q1A(R2) stability data: long-term at 25°C/60% RH and accelerated at 40°C/75% RH. Potency, disintegration and microbial results at each time point are documented in the stability report. For new formulations, we can run a 3-month accelerated study before launch and continue long-term testing in parallel.
Do you provide DDP shipping and who handles customs clearance?+
Yes, we can quote DDP for selected destinations, which means we arrange freight, insurance, export clearance, import duties and final delivery. The buyer still needs to confirm that the product can be lawfully imported and sold in the destination market, including any product notification or registration. For EXW and FOB terms, the buyer or their freight forwarder handles import clearance and duties. We provide the commercial invoice, packing list, COA and certificate of origin to support clearance.
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.