Custom and private label gummy manufacturing, coordinated from our U.S. office.
Sucotond USA gives U.S. brands a Brooklyn point of contact for gummy project intake, quotation and document coordination. Manufacturing is performed at the Sucotond Guangzhou facility; formula, gummy base, packaging, testing, MOQ and timing are confirmed for the actual brief.
Sucotond USA is our factory's U.S. sales and project-coordination office. Products are manufactured by our factory.
Quick Facts
Choose the manufacturing path that matches the brief.
A useful quote starts by separating an existing formula direction from a modified or fully custom project. None of the three paths implies ready inventory, a universal MOQ or a fixed lead time.
Private label starting point
Begin with an existing product-category direction, then confirm the exact formula version, serving, gummy base, flavor, shape, package, label responsibility, destination market and document set.
Quote trigger: selected category, package, target quantity and market are clear enough for written review.
Modified formula
Change the active level, serving design, pectin or gelatin direction, sweetener system, flavor, shape or package. Each change is screened for process, sensory, testing and stability consequences.
Quote trigger: the requested differences and non-negotiable label requirements are stated.
Custom formulation
Start from the intended actives, amounts, claims boundary, target consumer, market and commercial format. Feasibility comes before a price or schedule commitment.
Quote trigger: a non-confidential brief identifies the formula target, market, package and expected volume.
Before requesting proposals, use the gummy manufacturer RFQ template and Excel workbook; normalize suppliers with the quote and landed-cost calculator; review the MOQ, lead-time and cost guide; and verify the proposed facility with the 24-point supplier checklist.
Built for high active load, not just standard gummies
High-load functional gummies fail more often in production than in the lab. Our factory evaluates formulations against real process conditions so approved samples can be assessed for scale-up. Facility configuration, line fit and project scope are confirmed during qualification.
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.
COA-Ready Documentation
Batch-level records and third-party testing support traceability from raw material through finished goods.
Technical Specifications
| Parameter | Available Options |
|---|---|
| Colloidal system | Pectin-based — vegetarian-friendly and high-temperature resistant |
| Sugar system | Sugar-free, sugar-alcohol based (maltitol) · optional water-soluble dietary fiber at 5–10 g per serving |
| Gummy weight | 4–5 g per piece (recommended) |
| Serving format | 3 pieces per serving · 30-count and 45-count containers |
| Active-load review | Formula-specific; feasibility depends on the active, process, serving format and finished-product evidence. |
| Active categories | Creatine · Magnesium · Magnesium + Ashwagandha · CoQ10 · Vitamin D3+K2 · Collagen |
| Flavor options | Mango · Pineapple · Orange · Raspberry · Blueberry · Strawberry |
| Coloring | Natural sources — curcumin, carotene, fruit juice concentrates |
| Surface treatment | Coated finish for supplement-grade appearance |
| Packaging formats | Bottles / cans (opaque recommended for color stability) · Stand-up pouches · Custom labels |
| Shelf-life target | Established for the approved formula and package through the agreed stability program |
| Minimum order quantity | Confirmed after formula, packaging, materials and volume review |
| Development timing | Confirmed after brief and material-readiness review |
| Production timing | Confirmed for the approved formula, packaging, materials, quantity and destination |
| Analytical testing | Defined per project — active content, micro, heavy metals and other panels specified to your requirement |
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.
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Production photography from our factory. *Sample-specific analytical results do not guarantee identical results for every formula or production lot.
See the production environment in motion
Watch the English-language factory interview for visual context on the gummy production environment, then use the separate verification record and project documents for qualification decisions.
The video does not approve a formula, batch, label, claim, shelf life, MOQ or delivery schedule.
From reviewed inputs to project-specific output
Four production stages, each with defined in-process checks. Consistency is built through process control — not caught at final inspection.
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.
- Identity and potency confirmation against COA
- Microbiological screening
- Heavy metals verification
- Quarantine until QC release
Weighing & Pre-Process Control
Precision weighing under documented tolerances with second-person cross-check. Pre-mix parameters are locked before the batch advances.
- Documented weight tolerances per component
- Two-person verification on actives
- Batch record initiated and signed
- Pre-mix homogeneity check
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.
- Cooking temperature curve monitoring
- Deposit weight sampling at set intervals
- Drying room temperature & humidity control
- Moisture / water activity verification
Packaging & Release Checks
Fill-weight, appearance, documentation and traceability requirements are defined in the project-specific quality and release plan.
- Fill count / net weight verification
- Visual defect inspection
- Seal integrity check
- Lot coding & batch record closeout
Testing is evaluated within its project-specific scope
Practical active load is formula-specific and must be supported by the evaluated active, process, serving format and finished-product evidence. No sample result is presented here as a factory-wide capability claim.
Formula and serving scope
Define the active form, target dose, serving design, base system and finished-product specification before selecting tests.
Batch and sample traceability
Any result must be tied to the stated sample, batch, method, date and issuing party before it can support a claim.
Controlled document scope
The project-specific release-document set is confirmed in writing after quality, formula and destination-market review.
Document boundary: Source-document review may be available for qualified projects, subject to document-owner approval, laboratory terms and sample-specific scope. No certificate or test result is represented until its owner, scope and validity are verified.
Private label formats ready for U.S. brands
Product-specific feasibility paths for private label and custom gummy projects, with formula, evidence, label and package decisions confirmed per project.
Creatine Gummies
Sports nutrition format engineered for high creatine load without sacrificing chew texture or shelf stability.
View specifications →Magnesium Gummies
Magnesium form, elemental basis, serving mass and sensory limits are reviewed for the exact buyer brief.
View specifications →CoQ10 Gummies
CoQ10 material identity, label basis, analytical method, package and stability evidence are reviewed together.
View specifications →Custom Formula Vitamin D3 + K2 Gummies
D3 and K2 forms, individual amounts, source requirements, uniformity plan, package and U.S. label scope are defined per project.
Review custom-formula requirements →Collagen Beauty Gummies
Collagen species and source, serving mass, dietary-positioning, sensory criteria and package are buyer-defined inputs.
View specifications →Custom High-Load Development
For actives pushed beyond standard gummy concentration — evaluated for feasibility before any commitment to tooling.
View specifications →Magnesium + Ashwagandha Gummies
Elemental magnesium, botanical identity, marker basis, serving load, testing and U.S. claim review mapped as one project.
Review the combination brief →Turmeric & Curcumin Gummies
Custom development starts with ingredient identity, label basis, serving, sensory system, test plan and package.
Request feasibility →Probiotic Gummies
Custom development starts with strain identity, CFU time point, process exposure, method, package and storage.
Request feasibility →Functional Mushroom Gummies
Custom development starts with species, material basis, extract or powder, marker method, gummy matrix and package.
Request feasibility →Omega-3 EPA/DHA Gummies
Custom development starts with source, EPA/DHA basis, material form, oxidation methods, gummy matrix and package.
Request feasibility →Inositol Gummies
Custom development starts with named isomers, individual amounts, ratio, serving load, method, gummy matrix and label.
Calcium Gummies
Compound identity, elemental calcium, serving load, assay, label, package and stability are reviewed as one project.
Request feasibility →Iron Gummies
Iron salt, elemental amount, matrix interactions, assay, warning review and commercial package stay traceable.
Request feasibility →Vitamin C Gummies
Source, declared nutrient, acidity, assay, package and stability evidence are connected before commitment.
Request feasibility →Glutathione Gummies
Ingredient form, declared amount, finished-product assay, package and shelf-life evidence are mapped before commitment.
Request feasibility →Ashwagandha Gummies
Species, plant part, extract and withanolide basis, serving, test method, package and claims are separated before quote review.
Request feasibility →Who handles what
Manufacturing capability sits at our factory. 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
- U.S. coordination on Eastern Time; next steps confirmed after internal review
- 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 our production facility
- Formulation development and feasibility review
- Pilot validation and process parameter locking
- Commercial-scale production and batch control
- Quality-system and facility-document requirements
- Third-party testing coordination
- Project-specific release-document requirements
Sucotond USA is our factory's U.S. sales and project-coordination office. Products are manufactured by our factory. Project-specific facility and document requirements are reviewed before qualification. No certificate is represented until its owner, scope and validity are verified.
See the Brooklyn office and Guangzhou factory responsibility map, compare custom gummy manufacturing feasibility programs, use the stage-by-stage buyer resource center, or read the full library of evidence-backed gummy manufacturing guides.
What feasibility review covers by category
Each project is reviewed against formula, serving design, packaging, testing, material readiness, volume and destination. No prior-project result is represented here.
Load and serving review
Ingredient-form and sensory review
Acid-load and process review
These are illustrative review topics, not historical customer cases, commercial outcomes or timing commitments.
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 non-confidential concept, target actives, dosage and volume with our New York team for internal review.
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.
Questions buyers ask first
Is Sucotond USA the manufacturer?
Sucotond USA is our factory's U.S. sales and project-coordination office. Products are manufactured by our factory. Project-specific facility and document requirements are reviewed before qualification; no certificate is represented until its owner, scope and validity are verified.
What is your minimum order quantity?
MOQ is confirmed in writing after formula, packaging, material-readiness and volume review.
What are your lead times?
Development and production timing are confirmed after the brief, formula, packaging, materials, quantity and destination are reviewed. Freight and customs time are additional.
What documentation do you provide with each batch?
The project-specific release-document set is confirmed in writing after quality, formula and destination-market review. Source-document review may be available for qualified projects, subject to document-owner approval, laboratory terms and sample-specific scope.
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. Active-content, microbiological, heavy-metals and other requirements are considered against the formula, destination market and buyer specification before the testing plan is confirmed.
Start your gummy project
Share non-confidential product concept, target actives and volume for internal review. Formula, packaging, materials, quantity and destination are evaluated before any project-specific quote or commitment.
Brooklyn, NY 11214