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.
Quick Facts
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.
Active inclusion beyond standard gummy formats, developed with process feasibility and texture stability considered from the start.
Pilot validation before commercial scale, reducing the gap between the sample you approve and the batch you receive.
Critical process variables are controlled and monitored, so repeat runs hold texture, potency and appearance.
Batch-level records and third-party testing support traceability from raw material through finished goods.
| 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 |
| Evaluated active load | Up to 40% in development work; reported 34.6–36.2% for the creatine samples listed below. Practical limits vary by active and formula. |
| 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 | Up to 24 months, subject to formula-specific stability support |
| Minimum order quantity | 5,000 bottles |
| Sample lead time | 7–14 days |
| Production lead time | 7–15 days after sample approval, depending on order quantity |
| Analytical testing | Defined per project — active content, micro, heavy metals and other panels specified to your requirement |
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 manufacturing partner's facility. *Sample-specific analytical results do not guarantee identical results for every formula or production lot.
Four production stages, each with defined in-process checks. Consistency is built through process control — not caught at final inspection.
Incoming actives and excipients are checked against COA specification before release to the floor. Nothing enters production on a supplier's word alone.
Precision weighing under documented tolerances with second-person cross-check. Pre-mix parameters are locked before the batch advances.
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.
Fill weight, appearance and documentation are verified before sealing. Every lot remains traceable from raw material lot through to the shipment that reaches you.
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.
Confirms actual active content against label claim — the number a buyer's own QA team will re-test on arrival.
Records tie sample codes, batch numbers and test dates together, supporting traceability from R&D to mass production.
Testing feeds back into formulation and process refinement rather than serving as a one-time pass/fail gate.
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.
Established formulations available for private label, plus custom development where the active load or format demands it.
Sports nutrition format engineered for high creatine load without sacrificing chew texture or shelf stability.
View specifications →Glycinate and citrate formats for sleep and relaxation positioning, balanced for taste at higher mineral loads.
View specifications →Heart health and cellular energy formats built for active stability across the stated shelf life.
View specifications →Daily bone and immune support — a high-volume repeat-order category for U.S. retail and subscription DTC.
View specifications →Beauty-from-within positioning with private label packaging options suited to DTC and specialty retail.
View specifications →For actives pushed beyond standard gummy concentration — evaluated for feasibility before any commitment to tooling.
View specifications →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.
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.
Representative private label projects run at the partner facility for supplement brands in the U.S. and EU.
Projects shown were executed at our manufacturing partner's facility. Sucotond USA manages U.S.-side account handling and project coordination for this partnership.
Six stages designed so nothing is lost in the handoff between U.S. account management, overseas formulation, and delivery.
Share concept, target actives, dosage and volume with our New York team. No overnight wait for a first response.
The formulation team assesses active load, stability, taste balance and process compatibility before quoting.
Samples produced under production-representative conditions, shipped to you for evaluation and approval.
Process parameters locked and validated at pilot scale to confirm manufacturability before full production.
Commercial run executed under documented controls with batch-level monitoring and record keeping.
Shipment and delivery are coordinated with COA and batch records. Reorder timing is planned around your forecast and production schedule.
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.
5,000 bottles for standard private label formats. Reorder quantities and timing depend on the formula, packaging plan and production schedule.
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.
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.
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.
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.
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.
Send your product concept, target actives and volume. Our New York team will confirm feasibility, pricing and lead time.