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Contract Manufacturing · Private Label Functional Gummies

Private label gummies built to hold spec at high active load.

Third-party records for evaluated creatine samples show 34.6–36.2% active content. Formulas are developed against production-representative conditions to reduce the gap between the sample you approve and the commercial batch. Sucotond USA gives U.S. brands a New York point of contact from feasibility review through delivery.

Sucotond USA handles U.S. sales and project coordination. Manufacturing is performed at our partner's certified overseas facility.

Filled and capped functional gummy bottles on the finished goods line Quick Facts
Evaluated active loadUp to 40%*
Minimum order quantity5,000 bottles
Sample lead time7–14 days
Production lead time7–15 days
DocumentationCOA + batch records
Partner facility statusFDA registered · NSF GMP · ISO 22000
U.S. account handlingNew York, ET hours
5,000+ m²
Facility area
6+
Automated lines
90+
Production staff
40%*
Evaluated active load
5
Facility certifications
Certifications held by our manufacturing partner's production facility
FDA Food Facility RegisteredREGISTRATION IS NOT FDA APPROVAL GMPNSF GMP CertifiedVALID 2026 HACCPHACCP CompliantVALID 2027 ISO 22000ISO 22000VALID 2027 BRCGSBRCGS CertifiedVALID 2026
Manufacturing Capability

Built for high active load, not just standard gummies

High-load functional gummies fail more often in production than in the lab. Our partner facility — 5,000 m², 6+ automated lines, 90+ production staff — develops formulations against real process conditions so approved samples survive scale-up.

⚗️

High-Load Formulation

Active inclusion beyond standard gummy formats, developed with process feasibility and texture stability considered from the start.

📐

Sample-to-Production Alignment

Pilot validation before commercial scale, reducing the gap between the sample you approve and the batch you receive.

🔁

Batch Consistency

Critical process variables are controlled and monitored, so repeat runs hold texture, potency and appearance.

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COA-Ready Documentation

Batch-level records and third-party testing support traceability from raw material through finished goods.

Technical Specifications

ParameterAvailable Options
Colloidal systemPectin-based — vegetarian-friendly and high-temperature resistant
Sugar systemSugar-free, sugar-alcohol based (maltitol) · optional water-soluble dietary fiber at 5–10 g per serving
Gummy weight4–5 g per piece (recommended)
Serving format3 pieces per serving · 30-count and 45-count containers
Evaluated active loadUp to 40% in development work; reported 34.6–36.2% for the creatine samples listed below. Practical limits vary by active and formula.
Active categoriesCreatine · Magnesium · Magnesium + Ashwagandha · CoQ10 · Vitamin D3+K2 · Collagen
Flavor optionsMango · Pineapple · Orange · Raspberry · Blueberry · Strawberry
ColoringNatural sources — curcumin, carotene, fruit juice concentrates
Surface treatmentCoated finish for supplement-grade appearance
Packaging formatsBottles / cans (opaque recommended for color stability) · Stand-up pouches · Custom labels
Shelf-life targetUp to 24 months, subject to formula-specific stability support
Minimum order quantity5,000 bottles
Sample lead time7–14 days
Production lead time7–15 days after sample approval, depending on order quantity
Analytical testingDefined per project — active content, micro, heavy metals and other panels specified to your requirement
Inside the Facility

The production environment behind your order

From jacketed cooking kettles through depositing, filling, capping and labeling — the line your private label run actually passes through.

Jacketed stainless cooking and mixing kettle with gummy slurry under agitation 01
Cooking & Mixing — jacketed kettles with controlled temperature curves
Clean room packaging hall with multihead weighers and bottling conveyor 02
Packaging Hall — multihead weighing and bottling
Depositing head feeding gummy slurry into the hopper trough 03
Depositing Head
Brass mold plates being filled with gummy slurry on the depositing line 04
Mold Depositing
Bottle filling line with cap feeder and gummies entering bottles 05
Bottle Filling
Automated dual-head capping machine with control panel 06
Capping & Sealing
Rotary labeling machine applying labels to filled bottles 07
Labeling
Capped and filled gummy bottles moving along the finished goods conveyor 08
Finished Goods Line

Production photography from our manufacturing partner's facility. *Sample-specific analytical results do not guarantee identical results for every formula or production lot.

Manufacturing Process

From verified inputs to controlled output

Four production stages, each with defined in-process checks. Consistency is built through process control — not caught at final inspection.

01

Raw Material Verification

Incoming actives and excipients are checked against COA specification before release to the floor. Nothing enters production on a supplier's word alone.

In-Process Controls
  • Identity and potency confirmation against COA
  • Microbiological screening
  • Heavy metals verification
  • Quarantine until QC release
02

Weighing & Pre-Process Control

Precision weighing under documented tolerances with second-person cross-check. Pre-mix parameters are locked before the batch advances.

In-Process Controls
  • Documented weight tolerances per component
  • Two-person verification on actives
  • Batch record initiated and signed
  • Pre-mix homogeneity check
03

Cooking, Depositing & Drying

The stage where high-load formulas succeed or fail. Temperature curves, deposit weight and drying conditions are monitored in real time to hold both texture and active stability.

In-Process Controls
  • Cooking temperature curve monitoring
  • Deposit weight sampling at set intervals
  • Drying room temperature & humidity control
  • Moisture / water activity verification
04

Packaging & Release Checks

Fill weight, appearance and documentation are verified before sealing. Every lot remains traceable from raw material lot through to the shipment that reaches you.

In-Process Controls
  • Fill count / net weight verification
  • Visual defect inspection
  • Seal integrity check
  • Lot coding & batch record closeout
Third-Party Testing

Lab records that verify what's actually in the gummy

For high-load formats, active content is the claim buyers scrutinize hardest. The records below are third-party lab analyses retained by our manufacturing partner for evaluated samples. Full reports available on request.

Result — Active Load
34.6%
Sample nameCreatine Monohydrate Gummies
Sample code727-2026-00005570
Batch no.25031201
Report dateMar 19, 2026
Result — Active Load
36.2%
Sample nameCreatine Gummies
Sample codeBSFE2501139-001
Batch no.25031201
Report dateMar 20, 2026
Result — Active Load
3.8×10² mg/g
Sample nameCreatine Gummies
Sample codeJ-00524470
Batch no.25031201
Report dateMar 24, 2026
🎯

Formula Verification

Confirms actual active content against label claim — the number a buyer's own QA team will re-test on arrival.

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Batch & Sample Traceability

Records tie sample codes, batch numbers and test dates together, supporting traceability from R&D to mass production.

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Validation-Driven Development

Testing feeds back into formulation and process refinement rather than serving as a one-time pass/fail gate.

Request Full Lab Reports Complete PDF reports sent on request for qualified project inquiries.

Testing statement: Third-party testing records apply only to the corresponding evaluated samples and must be read in the context of the specific sample code, testing methodology and report date. These records do not constitute product certification or platform endorsement. Full reports available on request under laboratory usage terms.

Product Lines

Private label formats ready for U.S. brands

Established formulations available for private label, plus custom development where the active load or format demands it.

How We Work

Who handles what

Manufacturing capability sits at the partner facility. U.S. sales, project intake and documentation requests are coordinated from New York, with technical questions routed to the formulation team.

Handled in New York

  • Target response within one business day on Eastern Time
  • Feasibility questions routed straight to the formulation team
  • Sample coordination and project management
  • Quote, spec sheet and documentation requests
  • USD quoting and commercial coordination
  • Shipping-document and delivery coordination

Handled at the partner facility

  • Formulation development and feasibility review
  • Pilot validation and process parameter locking
  • Commercial-scale production and batch control
  • Quality systems and facility certifications
  • Third-party testing coordination
  • Batch documentation and COA issuance

Sucotond USA is the U.S. sales and project coordination partner. It is not the manufacturing entity and does not itself hold the facility certifications listed above.

Selected Projects

Manufacturing cases from our partner facility

Representative private label projects run at the partner facility for supplement brands in the U.S. and EU.

Sports Nutrition

Creatine Gummies for U.S. Sports Brand

Challenge
5 g active load with stable chew texture
Result
30,000 bottle pilot production
Timeline
5 weeks
Wellness

Magnesium Glycinate Gummies for U.S. Market

Challenge
200 mg elemental magnesium with balanced taste
Result
Third-party lab verified
Timeline
6 weeks
Functional Gummies

Apple Cider Vinegar Gummies for EU Brand

Challenge
Strong vinegar taste masking
Result
Scaled to launch production
Timeline
4 weeks

Projects shown were executed at our manufacturing partner's facility. Sucotond USA manages U.S.-side account handling and project coordination for this partnership.

Engagement Process

How a project runs, start to delivery

Six stages designed so nothing is lost in the handoff between U.S. account management, overseas formulation, and delivery.

Project Brief — NY Intake

Share concept, target actives, dosage and volume with our New York team. No overnight wait for a first response.

Formulation Feasibility

The formulation team assesses active load, stability, taste balance and process compatibility before quoting.

Sample Development

Samples produced under production-representative conditions, shipped to you for evaluation and approval.

Pilot & Process Alignment

Process parameters locked and validated at pilot scale to confirm manufacturability before full production.

Production & Batch Control

Commercial run executed under documented controls with batch-level monitoring and record keeping.

Delivery & Reorder

Shipment and delivery are coordinated with COA and batch records. Reorder timing is planned around your forecast and production schedule.

FAQ

Questions buyers ask first

Is Sucotond USA the manufacturer?

No. Sucotond USA is the U.S. sales and project coordination partner. Production takes place at our manufacturing partner's certified facility. We manage the U.S. relationship, account handling and delivery coordination. The facility certifications listed on this site are held by the manufacturing partner, not by Sucotond USA.

What is your minimum order quantity?

5,000 bottles for standard private label formats. Reorder quantities and timing depend on the formula, packaging plan and production schedule.

What are your lead times?

Samples typically ship in 7–14 days. Production is typically 7–15 days after sample approval and material readiness, depending on formula, packaging and order quantity. Freight and customs time are additional.

What documentation do you provide with each batch?

Certificate of Analysis, batch records and lot traceability documentation. Third-party lab reports for active content verification are available on request under laboratory usage terms.

Do you support custom formulation?

Yes. Custom formulas are evaluated for manufacturability first — active load, stability and process compatibility — before quoting, so projects are not scaled into problems that only appear at commercial volume.

Who handles import and customs clearance?

Shipping terms and importer-of-record responsibilities are agreed in the quote. We coordinate the required commercial and product documentation before shipment so your customs broker can review the file set in advance.

What analytical testing is included?

Testing scope is defined per project rather than by a fixed panel — B2B buyers each have their own requirements. Active content, microbiological and heavy metals testing are all available; tell us what your QA team or retail channel requires and we will build the testing plan around it.

Request a Quote

Start your gummy project

Send your product concept, target actives and volume. Our New York team will confirm feasibility, pricing and lead time.

U.S. Office
7624 17th Ave
Brooklyn, NY 11214
Business Hours
Monday–Friday, 9:00–18:00 ET
Target Response Time
Within one business day

By submitting, you agree that Sucotond USA may use these details to evaluate and respond to your project inquiry. Do not include confidential formula details until an NDA is in place. Privacy notice.

Thanks — your inquiry is in.
Our New York team will follow up within one business day with feasibility notes and pricing.
WhatsApp+1 (347) 495-0089 Email Usinfo@sucotondusa.com