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Health Supplement Manufacturing services ,OEM/ODM Solutions
# End-to-End Nutraceutical Manufacturing
At Zoxizo, we provide a fully integrated nutraceutical manufacturing solution covering every step from custom formulation design to global logistics and compliance documentation. Unlike generic contract manufacturers, our strength lies in combining GMP-certified production lines, advanced R&D laboratories, and regulatory expertise to deliver supplements that meet strict international standards while remaining cost-competitive and scalable.
Our production facilities include ten-thousand-grade cleanrooms with automated capsule filling, tablet compression, powder blending, gummy molding, and liquid bottling lines. Every batch undergoes real-time in-process quality control (IPQC), ensuring precise dosing, uniform appearance, and stable shelf-life.
Clients can choose from capsules, tablets, powders, gummies, liquid drops, and functional shots, each supported by robust formulation libraries with over 5,000 validated formulas for immunity, weight management, sports nutrition, anti-aging, and cognitive health.
Beyond production, we support multi-market compliance including FDA, HACCP, ISO, Halal, Kosher, Organic, and EU regulations. For cross-border e-commerce brands, we provide Amazon- and Shopify-ready labels, packaging design in multiple languages, and even guidance for FBA labeling and customs clearance.
Whether you require small-batch pilot runs for market testing or dedicated high-volume lines for large-scale launches, Zoxizo offers flexible MOQs, 3–7 day prototyping, and end-to-end project management to minimize time-to-market while maintaining rigorous quality standards.
Capsule Filling & Polishing
At Zoxizo, our capsule manufacturing lines are designed for precision, speed, and regulatory compliance. We produce both gelatin and vegetarian HPMC capsules in sizes ranging from 000 to 4#, meeting diverse dosage needs across markets. Each line integrates automated capsule fillers, weight-check sensors, polishing units, and metal detectors, ensuring every capsule meets strict weight uniformity, microbial safety, and aesthetic quality requirements.
Our R&D team works closely with clients to define fill weight accuracy, excipient systems, and release profiles for functional products such as probiotics, herbal extracts, vitamins, and minerals. We provide fast-release, acid-resistant, and delayed-release options to meet functional claims and consumer preferences.
Quality assurance involves disintegration and dissolution testing under USP and EP standards, microbial screening, and stability studies for moisture- or heat-sensitive ingredients. Batch traceability ensures COA documentation is available for every production run, critical for Amazon, EU, and Middle East regulatory compliance.
Our daily output capacity supports both small pilot runs and large-scale commercial orders, with flexible MOQs starting from 500 bottles for emerging brands. Combined with 3–7 day prototyping and 25–30 day production lead times, Zoxizo delivers capsules that are market-ready, compliant, and consistent in quality.
Tablet Pressing & Coating
Zoxizo provides high-speed rotary tablet compression combined with automated weight, hardness, and friability testing to manufacture tablets meeting GMP, USP, and EU quality standards. We offer diverse tablet formats including chewable, effervescent, fast-dissolving, and controlled-release options, tailored to functional claims and consumer usage preferences.
Our coating capabilities cover film coating, enteric coating, sustained-release layering, and aesthetic color coating, using excipients optimized for taste masking, moisture protection, and gastric resistance. This enables products to achieve improved stability, swallowability, and brand differentiation on retail shelves.
Each batch undergoes rigorous disintegration, dissolution, and uniformity assays, microbial limit tests, and stability studies under ICH conditions. Labels and packaging are fully compliant with FDA, EFSA, and GCC regulations, supporting Amazon-ready templates and multi-language artwork for cross-border e-commerce.
We also provide custom tablet embossing, variable dosage strengths, and coating thickness optimization, helping brands create visually distinctive, consumer-preferred tablets without compromising quality or regulatory standards.
Powder Blending & Packaging
Powders require homogeneous mixing, flavor consistency, and stable shelf-life to succeed in sports nutrition, meal replacement, and functional beverage categories. At Zoxizo, we employ V-blenders, double-cone mixers, and ribbon blenders with capacities suitable for pilot runs and commercial-scale production.
Our QA protocols include blend uniformity testing, moisture analysis, microbial screening, and particle size distribution studies before any batch proceeds to packaging. Packaging formats range from stick packs, aluminum foil pouches, and PET jars to bulk kraft bags, all customizable with multi-language labels and Amazon-compliant barcodes.
For flavor-sensitive products, we conduct sensory evaluations and stability trials under accelerated conditions, ensuring taste and color integrity during transport and storage. We also assist with flavor masking systems and natural sweetener integration for clean-label positioning.
Production lead times average 25–30 days post-prototype approval, with 3–7 day sampling cycles for new formulations. Flexible MOQs allow startups to launch single-SKU products, while established brands can scale multi-ton monthly volumes seamlessly.
Gummies & Chewables
Gummies and chewables offer high consumer compliance due to their pleasant taste and convenient dosage formats. Zoxizo manufactures gelatin- and pectin-based gummies with customizable shapes, colors, and flavors, enabling brands to differentiate in crowded markets.
Our production lines feature automated cooking, depositing, and cooling systems, guaranteeing accurate dosing, texture uniformity, and moisture control. Functional ingredients include vitamins, probiotics, collagen, herbal extracts, and Omega-3 oils, all validated for stability and label claims under GMP conditions.
We address formulation challenges such as hygroscopicity, heat sensitivity, and flavor masking using microencapsulation and controlled water activity systems. Packaging options span PET jars, pillow packs, and individually wrapped sachets, each meeting FDA, EFSA, and GCC regulations for e-commerce and retail distribution.
Pilot runs start from 1,000 jars, with flavor development cycles averaging 5–7 days. Larger clients benefit from high-speed lines capable of producing tens of thousands of gummies daily, ensuring consistent quality, global compliance, and scalable capacity.
Liquid Drops & Functional Shots
Liquid supplements deliver fast absorption, customizable dosing, and consumer convenience. Zoxizo specializes in tinctures, oral sprays, and single-serve shots produced under controlled-environment bottling lines with aseptic filling and inline quality checks.
Our R&D formulates for solubility, pH stability, and preservative efficacy, ensuring long shelf-life and flavor consistency. Advanced options like liposomal encapsulation and nano-emulsion systems boost bioavailability for fat-soluble vitamins, herbal extracts, and specialty actives.
We offer amber glass bottles, PET droppers, stick packs, and shot vials with tamper-evident seals, batch coding, and multi-language labeling. QA protocols include viscosity analysis, microbial screening, and accelerated stability testing to meet FDA, EFSA, and GCC requirements.
Pilot production begins at 1,000 bottles, scaling up to dedicated high-volume lines for established brands. Combined with cross-border logistics support and Amazon FBA compliance, Zoxizo ensures fast market entry and consistent global supply.
Custom Formulation & R&D
Zoxizo’s R&D team delivers evidence-based, regulatory-compliant formulations for categories spanning immunity, weight management, cognitive health, and anti-aging. Using a library of 5,000+ validated formulas and scientific literature databases, we design synergistic ingredient blends aligned with EFSA, FDA, and GCC standards.
The process begins with market trend analysis, competitor benchmarking, and clinical data review, followed by prototype development within 3–7 days. We conduct sensory evaluations, stability trials, and cost optimization studies to balance efficacy, consumer appeal, and commercial viability.
For premium products, we integrate patented or clinically substantiated ingredients, enabling science-backed claims and clean-label positioning. Technical dossiers include nutritional facts, COAs, and third-party testing options, facilitating Amazon listing approvals and EU product registration.
Our R&D services shorten time-to-market while ensuring quality, compliance, and scalability for both emerging startups and established nutraceutical brands.
QA Methodology & Traceability
Zoxizo operates under GMP, HACCP, and ISO 22000 frameworks, embedding QA across raw material sourcing, in-process controls, and finished product testing. Every batch follows a digital traceability system linking raw materials, production logs, and COA documentation.
Key QA checkpoints include:
- Raw Materials: COA verification, microbial limits, heavy metals, and pesticide residue screening.
- In-Process Control: Real-time weight checks, environmental monitoring, and batch record audits.
- Finished Products: Disintegration, dissolution, friability, stability, and label compliance reviews.
All test data aligns with USP, EP, and ICH guidelines, ensuring global market readiness. Clients receive full QA documentation for regulatory submissions, retailer audits, and Amazon verification programs.
By integrating preventive controls, risk-based inspections, and digital batch records, Zoxizo guarantees product safety, consistency, and regulatory compliance across every SKU.
Packaging Engineering
Zoxizo designs packaging solutions balancing functionality, cost, and brand aesthetics. Formats include HDPE/PET bottles, aluminum foil pouches, composite cans, stick packs, blister cards, and display cartons with tamper-evident features.
Our in-house design team provides Amazon-ready labeling templates, GS1 barcodes, and multilingual artwork to meet FDA, EFSA, and GCC compliance. Options like foil stamping, embossing, matte/gloss finishes, and custom Pantone colors help brands achieve premium shelf presence.
Low-MOQ digital printing supports pilot runs, while large orders benefit from offset printing economies of scale. Every batch undergoes seal integrity tests, dimensional checks, and visual inspections before shipment.
Packaging also meets FBA carton dimension, weight, and labeling standards, streamlining e-commerce logistics for global fulfillment.
Label & Regulatory Compliance
Cross-border supplement sales demand strict labeling compliance. Zoxizo ensures every SKU meets FDA 21 CFR, EFSA 1169/2011, and GCC labeling rules with fully audited artwork templates.
Our services include:
- Ingredient & Allergen Statements under FDA and EU rules.
- Nutrition Facts Panels aligned with target market standards.
- Health Claim Reviews for EFSA/FDA compliance.
- Barcode & Traceability Integration with GS1 databases.
We also assist with Halal, Kosher, Organic, and Non-GMO certifications, providing documentation for retailer onboarding, Amazon listing approvals, and customs clearance.
By merging regulatory expertise with in-house design capabilities, Zoxizo simplifies multi-market compliance for emerging and established brands.
Global Compliance & Certifications
Zoxizo’s facilities hold GMP, HACCP, ISO 22000, and FSSC 22000 certifications, validated by third-party audit bodies.
We support clients with:
- Halal & Kosher Certificates for Middle East and Jewish markets.
- Organic & Non-GMO Certifications for clean-label positioning.
- COAs & MSDS Documentation for every batch.
On-site audits welcome client QA teams, offering access to SOP libraries, validation reports, calibration logs, and CAPA records. We also share digital documentation for Amazon, EU, and GCC regulatory submissions.
Annual re-certifications and regulatory updates keep our facilities aligned with global food safety standards for uninterrupted export compliance.
Cross-Border Logistics & Fulfillment
Global distribution requires DDP shipping, customs clearance, and regulatory paperwork. Zoxizo integrates freight forwarding, tax compliance, and FBA routing for clients targeting US, EU, GCC, and APAC markets.
Our services cover:
- FDA-Registered Warehousing for Amazon FBA readiness.
- Import Permit Advisory for GCC and African markets.
- Cold Chain Logistics for temperature-sensitive SKUs.
- HS Code Classification & Tariff Guidance for customs efficiency.
We coordinate with DHL, FedEx, and regional carriers to balance lead time, shipping cost, and compliance risks, ensuring on-time, customs-cleared deliveries globally.
Industries & Use-Cases
Zoxizo provides a complete catalog of health supplements covering the most in-demand categories: hydration, weight management, anti-aging, immunity, gut support, sleep, liver/eye, hormonal balance, and kids/seniors. With more than 5,000 validated formulas, all manufactured under GMP standards, we offer flexibility across dosage forms—capsules, tablets, gummies, powders, softgels, and liquid drops. This wide portfolio allows B-end buyers such as Amazon sellers, retailers, and private-label brands to rapidly launch or expand their product lines with confidence in quality, compliance, and scalability.
No matter your goal, we have you covered. Choose from our extensive service offerings to get direct access to our state-of-the-art facilities and get best-in-class supplement products made for your business:
Heavy metal free • Free from artificial colors or flavors • Soy free • Gluten free • Nut free • Non-GMO • Lactose free
Frequently Asked Questions
Q1: What dosage forms does Zoxizo manufacture?
Zoxizo offers a full spectrum of dosage forms including capsules, tablets, powders, gummies, and liquid supplements. Our automated production lines integrate encapsulation, tablet compression, powder blending, gummy molding, and liquid bottling under GMP, HACCP, and ISO 22000 frameworks. We also support fast-release, delayed-release, and controlled-release technologies, enabling brands to customize formulations based on functional claims, consumer preferences, and market regulations. Whether you need small pilot runs or large commercial batches, we provide 3–7 day prototyping, full COA documentation, and Amazon- or EU-compliant labeling for cross-border sales.
Q2: Can Zoxizo assist with product formulation and R&D?
Yes. Our 20+ member R&D team specializes in custom formulations for immunity, weight management, sports nutrition, cognitive health, and anti-aging categories. We use a library of 5,000+ validated formulas, conduct stability studies, flavor optimization, and cost engineering, and ensure compliance with FDA 21 CFR, EFSA 1169/2011, and GCC regulations. For premium products, we integrate patented ingredients or clinically substantiated actives to support science-backed claims. Technical dossiers include nutritional facts, COAs, and Amazon/EU listing documentation, accelerating time-to-market while maintaining regulatory integrity.
Q3: What is your minimum order quantity (MOQ) for supplements?
MOQ depends on the dosage form, packaging format, and market requirements. Typical MOQs are: 1,000–5,000 bottles for capsules or tablets, 2,000–5,000 stick packs, 500–1,000 pouches or blisters, and 25–50 kg bags for bulk powders. We support low-MOQ pilot runs with digital printing for startups validating new SKUs, while established brands benefit from high-volume lines for monthly replenishments. All batches include COA documentation, stability data, and label compliance checks, ensuring every order—large or small—meets global quality and regulatory standards.
Q4: How does Zoxizo ensure product quality and regulatory compliance?
Quality assurance spans the entire supply chain, from raw material COA verification and in-process weight checks to finished product disintegration, dissolution, microbial limits, and heavy metal analysis under USP, EP, and ICH guidelines. We operate under GMP, HACCP, ISO 22000, and FSSC 22000 certifications, welcoming third-party audits and providing full traceability documentation for each batch. Our team also reviews label claims, allergen statements, and nutrition facts to ensure compliance with FDA, EFSA, GCC, and Amazon regulatory frameworks for seamless cross-border distribution.
Q5: Do you provide labeling and packaging design services?
Yes. Zoxizo offers in-house packaging engineering and label compliance support for bottles, jars, pouches, stick packs, and cartons. We deliver Amazon-ready labeling templates, multi-language artwork, and barcode integration aligned with GS1, FDA, EFSA, and GCC standards. Packaging options include foil stamping, embossing, tamper-evident seals, and custom Pantone colors for premium branding. For startups, we support low-MOQ digital printing, while large brands benefit from offset printing economies of scale with FBA-compliant carton dimensions, labeling, and palletization for e-commerce fulfillment.
Q6: Can Zoxizo handle cross-border logistics and customs clearance?
Absolutely. We coordinate DDP (Delivered Duty Paid) shipping, FDA-registered warehousing, customs documentation, and HS code classification for markets including US, EU, GCC, and APAC. Our logistics partners include DHL, FedEx, UPS, and regional carriers, balancing lead times, shipping costs, and regulatory risks. For Middle East and African markets, we assist with Halal certification, import permit advisory, and Arabic labeling. All shipments include COAs, batch records, and regulatory paperwork to ensure smooth customs clearance and platform listing approvals.
Q7: What certifications can you provide for supplements?
Zoxizo’s facilities maintain GMP, HACCP, ISO 22000, and FSSC 22000 certifications, with optional Halal, Kosher, Organic, Non-GMO, and Gluten-Free certifications available for qualifying formulations. Each batch comes with COAs, MSDS, and full traceability documentation, supporting Amazon, EU, and Middle East listing approvals. We welcome third-party audits and provide CAPA records, calibration logs, and training documentation for enterprise clients requiring supplier qualification and compliance evidence before onboarding.
Q8: How fast can you deliver samples and commercial orders?
Sample prototyping typically takes 3–7 days for standard formulas and 7–12 days for complex actives requiring special raw materials or flavor masking systems. Commercial production lead times average 25–30 days post-sample approval, depending on packaging lead times, order volume, and regulatory documentation. For urgent projects, we offer fast-track options with dedicated production lines and priority logistics routing, ensuring products meet launch deadlines, e-commerce listing windows, and retailer onboarding schedules without compromising quality or compliance.
Contract Manufacturing for Global Brands
We support large-scale production with ISO, GMP, and FDA facilities. Whether you’re a DTC brand, pharmacy chain, or global distributor, we offer full OEM support, strict QC, batch traceability, and long-term strategic cooperation.
Contact our OEM Advisor today and get a quote within 24 hours.
