Private label supplement manufacturing empowers brand owners, distributors, and retail chains to introduce market-ready, scientifically backed dietary supplements under their own brand name. By partnering with Zeon Lifesciences, businesses eliminate heavy capital expenditure in R&D infrastructure, specialized machinery, and regulatory overheads while maintaining complete brand ownership and premium product quality.
With over 38 years of formulation legacy, US FDA registration, and FSSC 22000 certification, Zeon offers end-to-end OEM and ODM services. From initial concept formulation and ingredient sourcing to analytical validation, stability testing, custom packaging, and international export documentation, our technical teams ensure seamless market entry for global buyers.
Scale quickly with market-proven base formulations, low minimum order quantities (MOQs), and validated shelf-life data.
Expand product portfolios into new dosage formats (spray, diskettes, effervescent tablets) without capital investment.
Launch high-margin private label dietary supplements backed by complete analytical Certificate of Analysis (COA).
Offer custom-branded therapeutic nutrition, probiotics, and phytopharma supplements designed for target clinical outcomes.
US FDA registered, FSSC 22000 (Intertek), WHO-GMP, HACCP, ISO 22000, FSSAI, AYUSH, and Halal certified manufacturing campus.
Instrumented quality control labs equipped with HPLC, GC, UV-Vis, and dissolution apparatus ensuring strict assay and purity standards.
Annual production capacity of 400M tablets, 140M capsules, 70M liquids, and 35,000 MT powders with fast batch turnaround.
Clients can select from over 850 commercialized formulations or work directly with our formulation scientists to engineer bespoke active ingredients, flavor profiles, and dose delivery formats:
An international wellness startup partnered with Zeon to introduce a specialized phytopharma supplement line targeting stress management and immunity in North America and Western Europe.
A established Middle Eastern distributor required rapid development of a multi-active probiotic and prebiotic formulation with guaranteed CFU strain survival throughout 24-month shelf life.
We produce tablets (film-coated, chewable, effervescent), hard gelatin/HPMC capsules, nutritional diskettes, powder blends in jars or sachets, sublingual sprays, and oral syrups across dedicated cleanroom facilities.
Yes, all parameters including active ingredient concentrations, excipients, natural/synthetic flavor systems, unit packaging (bottles, blisters, tubs, stick packs), and master outer cartons are fully customizable to meet destination market regulations.
Yes, our R&D lab provides R&D sample batches and pilot trials for physical evaluation, taste testing, analytical assay verification, and client approval prior to full commercial scale-up.
Our facility operates strictly under US FDA, FSSC 22000, and GMP standards. Every batch comes with a comprehensive Certificate of Analysis (COA), microbiological testing, heavy metal clearance, stability data, and export documents.
Consult with our technical R&D scientists and international regulatory specialists to review formulations, sample requests, minimum order quantities, and manufacturing lead times.
