Manufactured according to stringent clean-label food grade and cosmetic standards. Fully compatible with continuous blending lines, ready-to-mix sachets, and liquid RTD lines.
Eurofins laboratory-tested raw ube powder, standardized for high heat stability, vivid natural violet shades, and clean-label functional beverage integration.
Micro-ground roasted green tea powder delivering a nutty, roasted sensory profile. Low astringency ideal for nutricosmetic collagen wellness drink formulations.
First-harvest, shade-grown Japanese cultivar green tea milled to ultra-fine mesh (≤18 μm). Standardized for rich L-theanine and EGCG content.
Certified USDA and EU organic green tea powder. Multi-residue screened against BS EN 15662 guidelines with zero micro-contaminants.
100% natural, spray-dried purple sweet potato powder formulated for instant cold-water dispersion, dairy-free creaminess, and plant-based lattes.
Ultra-pure tripeptide-1 copper complex (99% HPLC assay) designed to synergize with hydrolyzed marine fish collagen in advanced topical anti-aging formulations.
100% water-soluble nitrate-dense beetroot juice concentrate. Acts as an instant natural ruby colorant and nitric oxide booster for fitness-collagen blends.
Pure ceremonial green tea powder produced with traditional granite stone milling. Supreme electric emerald green hue with balanced umami profile for high-end luxury SKU launches.
In the rapidly evolving landscape of bioactive dietary supplement and cosmeceutical manufacturing, Hydrolyzed Marine Fish Collagen Peptides (derived from sustainably sourced wild ocean fish skins and scales, primarily Gadus morhua and Tilapia mossambica) represent the pinnacle of bioavailability and bio-functional efficacy. Unlike bovine or porcine-derived structural gelatin, marine collagen comprises predominantly Type I collagen, the exact triple-helical fibrous protein found abundantly within human dermal layers, connective tendons, and skeletal architecture.
As an established manufacturing partner and primary OEM processing facility serving brand developers, pharmaceutical compounders, and high-volume contract packaging facilities in New York and the greater Northeast region, Xi'an Vexli Bio-Tech operates state-of-the-art enzymatic cleavage facilities. Through strictly calibrated multi-stage continuous enzymatic hydrolysis, we isolate specific bioactive tripeptide sequences—specifically Prolyl-Hydroxyproline (Pro-Hyp) and Hydroxyprolyl-Glycine (Hyp-Gly). These oligopeptides survive systemic gastrointestinal hydrolysis, signaling dermal fibroblasts directly through chemotactic triggers to upregulate endogenous collagen and hyaluronan synthesis.
Precision separation cuts yielding weight profiles from ≤1,000 Daltons to 3,000 Daltons. 92% of oligopeptides fall below the cellular absorption threshold, guaranteeing maximum enteric transport.
Patented vacuum steam deodorization and secondary carbon bed resin filtration removes all trace trimethylamine (TMA), ensuring completely neutral taste, clarity, and odorless dissolution in cold liquids.
Instantized agglomerated granules provide rapid surface wetting, zero foaming, zero clumping, and immediate transparency in clear functional beverages without adding artificial stabilizers.
| Analytical Parameter | Guaranteed Standard Specification | Testing Methodology (USP / FCC / EP) |
|---|---|---|
| Protein Content (Dry Basis) | ≥ 90.0% (Typically 93.5% - 95.0%) | Kjeldahl Method (Factor 5.55 / 6.25) |
| Average Molecular Weight Distribution | ≤ 1,000 Da (>80%) / ≤ 3,000 Da (>95%) | GPC (Gel Permeation Chromatography) - HPLC |
| Organoleptic Profile | Pure white to light ivory powder, odorless, completely neutral | Visual & Sensory Panel Assessment |
| Bulk Density | 0.30 g/ml - 0.45 g/ml (Agglomerated available: 0.20-0.30 g/ml) | USP <616> Method I |
| Transmittance (10% Solution) | ≥ 95.0% Clear, colorless aqueous solution | UV-Vis Spectrophotometer @ 430 nm |
| Heavy Metals (Pb, As, Cd, Hg) | Lead < 0.5 ppm, As < 0.5 ppm, Cd < 0.1 ppm, Hg < 0.05 ppm | ICP-MS (Strict NY Proposition 65 & FDA Limits) |
| Total Plate Count (TPC) | ≤ 1,000 cfu/g (Strict pathogen free: Salmonella/E.Coli Neg) | AOAC Official Microbiological Methods |
As one of the world's most influential commercial centers for beauty, health consciousness, and nutritional innovation, New York sets the benchmark for product formulators. From Manhattan’s boutique health bars and high-end aesthetic medical practices to Long Island’s large-scale contract manufacturing parks (cGMP dietary supplement facilities in Hauppauge, Ronkonkoma, and Melville), sourcing pure hydrolyzed marine fish collagen from an audited primary factory guarantees unmatched competitive advantages.
Designed specifically for Brooklyn and Manhattan clean-label beverage startups formulating clear sparkling collagen waters, beauty seltzers, ready-to-drink adaptogenic lattes, and functional cold-brew infusions that require total optical clarity and zero shelf-life sediment precipitation.
Long Island supplement plants demand uniform bulk density, superior free-flowing granulation, and anti-caking properties for high-speed multi-lane stick-pack machines, sachet lines, and 2-piece hard shell capsule fillers operating under strict 21 CFR Part 111 cGMP rules.
Serving New York’s medical spa distributors and cosmetic formulators blending oral peptide elixirs with topical Cosmetic Grade Blue Copper Peptide GHK-Cu for comprehensive inner-outer systemic dermal remodeling.
Modern procurement directors across New York are shifting decisively away from generic, land-animal bovine and porcine collagen sources toward premium marine peptides. Several structural market drivers underpin this regional transformation:
Headquartered in Xi'an, Shaanxi, Xi'an Vexli Bio-Tech Co., Ltd. combines advanced biotechnological manufacturing with deep raw-material supply integration. Backed by an annual export turnover of over US $29.5 Million and regular exports to 30+ countries, our infrastructure removes intermediary brokers, guaranteeing factory-direct batch consistency, comprehensive technical documentation, and rapid scale.
Independently verified on-site by SGS for operational cleanliness, quality management systems, raw material quarantine, and release compliance.
Dual Food Safety Management systems: ISO 22000 and HACCP certified, alongside full Halal, Kosher, and USDA / EU Organic processing scopes.
Owner of Invention Patent ZL 2014 1 0464649.9 and Utility Model Patent 14520048, driving extraction yield efficiency and purity controls.
Comprehensive custom formulation, custom molecular cutting, mesh sizing (80 to 450 mesh), private label stick-packaging, jars, and drums.
Direct answers addressing technical parameters, minimum commitments, testing protocols, and regulatory filings for US customs entry.
Our standard minimum order quantity for Hydrolyzed Marine Fish Collagen Peptides is 25 kg (one airtight fiber drum with double PE liners). For customized enzyme cuts, agglomerated instantized versions, or custom private label retail packing, MOQs generally start at 100 kg to 500 kg.
Every production batch undergoes strict Gel Permeation Chromatography (GPC) coupled with HPLC calibration against known peptide protein standards. Every shipment is accompanied by a batch-specific Certificate of Analysis (COA) detailing the exact percentage distribution of peptides under 1,000, 2,000, and 3,000 Daltons.
We employ a proprietary three-stage purification sequence: low-temperature ultra-filtration, activated carbon resin column adsorption to remove secondary amines, and multi-effect vacuum steam deodorization. The resulting hydrolysate yields an ODN score of 0, making it undetectable in plain water or subtle matcha drinks.
Yes. Due to ocean habitat sourcing and selective enzymatic extraction that leaves minerals behind, our marine collagen tests consistently below 0.1 ppm for Lead (Pb), Arsenic (As), Cadmium (Cd), and Mercury (Hg), well within California Proposition 65 limits and FDA Dietary Supplement cGMP guidelines.
Yes. We regularly handle FOB, CIF, and full DDP (Delivered Duty Paid) terms. We manage all export declarations, US Customs clearance, FDA Prior Notice filings, and inland linehaul trucking directly to your designated warehouse dock door in New York, New Jersey, or Connecticut.
Yes. We provide 50g–100g complimentary evaluation samples along with the active batch COA, Allergen Declarations, Non-GMO statements, and SDS to qualified formulators, R&D directors, and procurement managers before commercial contracting.
Whether you require bulk 25 kg drums for high-speed automated packaging lines or turnkey private-label formulations customized for the New York retail market, our bio-enzymatic specialists are available to discuss your specifications, provide full regulatory dossiers, and dispatch pilot samples.