LABEL
Your Formula.
Your Ingredient Stack.
No One Else’s.
Private label supplement manufacturing gives your brand something no white label program ever can — a formulation that belongs entirely to you. Built from the ground up by our R&D team, manufactured in GMP-certified facilities, and exported to 30+ countries under your name, your packaging, and your intellectual property.
When Your Brand Needs a
Formula Nobody Else
Can Replicate
Private label supplement manufacturing begins where white label ends. Instead of selecting from an existing catalogue and applying your brand name, private label means working directly with our formulation scientists to design an ingredient combination that exists nowhere else — built around your target customer, your health claim positioning, your competitive differentiation, and your intellectual property.
White label gets your product to market faster. Private label gets your brand to a position that no competitor can copy.
The result is a supplement formula that is legally yours — not shared across dozens of brands under the same catalogue SKU. Your formulation specification, your ingredient ratios, your proprietary stack. It goes into production only for you, and we protect that exclusivity throughout our relationship.
- Proprietary formulation developed by our R&D scientists — tailored to your brand and target market
- Ingredient sourcing coordinated directly from India’s botanical and nutraceutical origin suppliers
- Full brand identity development — logo, label design, packaging, regulatory-compliant panels
- GMP-certified production, batch-level quality testing, Certificate of Analysis on every run
- Regulatory compliance for FDA, TGA, MHRA, Health Canada, and EU food supplement directives
- International export with complete customs documentation — air or sea freight, door-to-door
Every Major Supplement
Category Available for
Custom Development
Our private label formulation network covers every major supplement category. Whether you are building a single hero product or a complete wellness range across multiple categories, our R&D team and manufacturing facilities support custom formulation development from concept through production-ready specification — entirely under your brand.
India is the single most important source in the world for standardised Ayurvedic botanicals. Our private label program gives you direct access to ashwagandha, shilajit, turmeric, brahmi, boswellia, moringa, shatavari, and 200+ additional herbs — sourced from authenticated Indian origin, extracted in our own facility, and incorporated into a proprietary blend built for your brand.
The global longevity supplement market is one of the fastest-growing supplement categories. Our private label program supports custom formulation of NMN, NR, trans-resveratrol, fisetin, pterostilbene, CoQ10, PQQ, spermidine, alpha-lipoic acid, and combination longevity stacks — each analytically verified for purity and potency before release.
Custom protein blends, proprietary pre-workout formulas, unique BCAA ratios, creatine combinations, and performance stack development. Clean label formulations, natural flavour and colour systems, third-party banned-substance testing. Built for brands targeting athletes, fitness enthusiasts, and the rapidly growing clean sports nutrition segment.
Custom adaptogen and nootropic formulations for the stress resilience, sleep quality, and cognitive performance categories. Proprietary magnesium glycinate complexes, L-theanine and ashwagandha stack formulas, custom melatonin release profiles, and branded cognitive support blends combining Ayurvedic botanicals with modern neuroscience-backed compounds.
Custom collagen peptide blends (Types I, II, III — bovine, marine, or plant-based), proprietary beauty-from-within formulas incorporating hyaluronic acid, biotin, silica, vitamin C, and astaxanthin. Joint health complexes combining glucosamine, chondroitin, MSM, and Indian botanicals including shallaki and boswellia in clinically-relevant dosages.
Custom multivitamin formulas, targeted mineral complexes, and single-nutrient supplements in the most bioavailable forms. Methylcobalamin B12, methylfolate, D3 + K2 MK-7, chelated minerals, and liposomal delivery systems. Prenatal and postnatal formulas developed to WHO nutritional guidelines and regional RDA specifications for USA, UK, EU, and Australian markets.
From Brief to
Branded Product
— Every Stage Mapped
Private label supplement development is a structured journey — not a single transaction. Each stage has clear inputs, defined outputs, and a client approval gate before the next stage begins. Nothing moves forward without your sign-off. You are involved at every decision point, with full visibility into formulation choices, ingredient sourcing, quality results, and packaging artwork before production commits.
Our formulation team conducts a structured discovery session covering your target consumer profile, primary health claim positioning, competitive landscape, ingredient preferences or restrictions, regulatory destination markets, packaging format, and budget parameters. This brief becomes the founding document for your formulation development — every ingredient decision made against it.
- Formulation brief document
- Preliminary regulatory assessment for destination markets
- Preliminary ingredient feasibility report
- Indicative pricing and timeline estimate
Our scientists develop your formulation from the brief — selecting ingredients, determining clinically-meaningful dosages, evaluating bioavailability and interaction profiles, confirming regulatory compliance for your target markets, and creating the full ingredient specification. Multiple formulation options presented where relevant, with transparent rationale behind every ingredient choice. You review, refine, and approve before prototype production begins.
- Full formulation specification document
- Ingredient sourcing plan and supplier provenance
- Regulatory compliance review per destination market
- Dosage justification and health claims assessment
Small-batch sample production of your approved formulation for physical evaluation — appearance, texture, taste (where applicable), capsule or tablet characteristics, dissolution, and initial packaging mockup review. Third-party laboratory testing of samples for potency verification, contaminant screening, and stability markers. You evaluate, request refinements if needed, and issue formal written approval before full production is committed.
- Physical product samples — 50 to 200 units
- Sample Certificate of Analysis
- Packaging mockup for label approval
- Third-party potency and contaminant test report
Concurrent with sample evaluation, our design team develops your brand identity and product label artwork. Logo creation, colour palette, label design, supplement facts panel (formatted to FDA, TGA, or EU standards), allergen statements, QR code integration, barcode placement, and carton artwork. Multiple design rounds with revision cycles until you are satisfied. All artwork files delivered in print-ready format — yours to keep and use across any future supplier.
- Logo and brand identity files (AI, PDF, PNG)
- Product label print-ready artwork
- Regulatory-compliant supplement facts panel
- Packaging carton artwork (if applicable)
Your approved formulation enters full-scale production at the appropriate GMP and ISO 9001:2015 certified facility within our manufacturing network. Complete batch record documentation throughout. In-process quality monitoring at every production stage. Environmental monitoring, equipment calibration records, and yield verification. Finished batch undergoes comprehensive laboratory testing — identity, potency, purity, microbiology, heavy metals, and pesticide residue screening — before commercial release authorisation.
- Full batch production records
- In-process quality monitoring reports
- Comprehensive Certificate of Analysis
- Third-party independent test report (Growth and Enterprise tiers)
Released product filled into bottles or containers, your label applied and inspected, tamper-evident sealed, and packed into export cartons with FNSKU barcoding, GS1 labelling, and shipper identification as required. Complete export documentation package prepared: commercial invoice, packing list, Certificate of Analysis, MSDS, Certificate of Origin, phytosanitary certificates (herbal products), and country-specific regulatory documents. Sea freight or air cargo coordinated door-to-door to your warehouse, Amazon FBA fulfillment center, or third-party logistics provider.
- Filled, labelled, and sealed finished product
- Complete export documentation package
- Shipment tracking and customs clearance coordination
- Door-to-door delivery to your specified destination
R&D That Builds
Differentiation
Into the Formula Itself
Formulation is where most private label manufacturers in India stop thinking and start mixing. At Jireh Nutrition Hub, formulation R&D is a scientific process — not a catalogue selection exercise with your logo applied. Every custom formula we develop for a private label client is built around evidence: clinical research on ingredient efficacy, bioavailability data, dose-response relationships, and the regulatory context of your destination market.
Our scientists have worked across pharmaceutical, nutraceutical, and Ayurvedic categories for over a decade. That means they understand how botanical matrix effects influence bioavailability, which ingredient combinations produce synergistic outcomes, and which health claims are defensible in each of your target markets — before a single gram goes into a blender.
A Formula Without a Brand
Is Just a Product.
We Build Both.
Private label manufacturing is not just about what is inside the bottle. It is about the entire brand experience that communicates your product’s value before a consumer ever opens it. Our design and regulatory team develop label artwork, brand identity materials, and compliance documentation that meets the requirements of every major international market — delivered as ready-to-print, camera-ready files that belong entirely to you.
Logo design, colour palette, typography system, and brand style guide. Whether you are building a new brand from zero or extending an existing one into supplements, our designers create a visual identity that positions your product correctly in your target market — from minimalist clean-label aesthetics to bold wellness branding or premium Ayurvedic positioning.
Front panel design, supplement facts panel, ingredient list, allergen declarations, directions for use, and all required regulatory disclosures — laid out in compliance with the specific labelling regulations of your target market. FDA 21 CFR 101, TGA labelling requirements, EU 1169/2011, and Health Canada format all handled by our team as standard.
Secondary packaging design for boxes, display cartons, and outer shipper artwork. Custom insert cards, leaflets, and unboxing experience development for DTC and premium retail brands. Amazon FBA-compliant packaging dimensions and FNSKU barcode integration built into every carton specification as standard procedure.
Private Label Programs for
Brands at Every Stage
of Growth
Custom formulation development is a significant commitment — for us and for you. Our three-tier private label structure ensures that the investment in R&D, sampling, regulatory review, and brand development is appropriate to your current stage of growth, your order volume, and the level of differentiation your brand strategy requires. Every tier includes complete formulation ownership and exclusivity.
- Custom formulation development — 1 SKU
- Ingredient sourcing coordination
- Standard dosage form (capsule or tablet)
- Basic label design and supplement facts panel
- GMP-certified production
- Certificate of Analysis per batch
- Standard sea freight shipping
- 10–12 week development timeline
- Full formulation IP ownership — yours
- — Third-party independent testing
- — Custom packaging or molds
- — Multi-SKU formulation range
- Custom formulation R&D — up to 3 SKUs
- Advanced bioavailability options (Phytosome, liposomal)
- All dosage forms — capsule, softgel, powder, gummy
- Professional full brand identity development
- GMP + third-party independent testing
- Custom packaging and closure options
- Priority production scheduling
- Air freight coordination available
- 8–10 week development timeline
- Dedicated account manager
- Amazon FBA-ready carton marking
- Regulatory compliance review — 2 markets
- Fully custom multi-SKU range development
- Proprietary ingredient blend co-development
- Custom molds and branded primary packaging
- Complete brand ecosystem design
- Advanced testing — HPLC, heavy metals, pesticide residue
- Full regulatory dossier — FDA, TGA, MHRA, EFSA
- Volume pricing with margin optimisation
- Expedited production options
- Dedicated senior partnership team
- Strategic botanical sourcing agreements
- Long-term supply chain continuity planning
- Patent-readiness support for novel formulas
Every Batch Released
Only After It Passes.
No Exceptions.
In private label manufacturing, quality is not an optional premium — it is the entire value proposition. When your name is on the label, every quality failure is your brand’s failure. Our quality control framework ensures that nothing carrying your label was produced, tested, or released without passing the same rigorous protocol we apply to every batch across every client in our network.
All manufacturing facilities within the Jireh network operate under GMP and WHO-GMP certification — the internationally recognised standard for pharmaceutical and nutraceutical production quality. Every batch produced under full documented procedures: equipment calibration records, environmental monitoring, personnel training logs, deviation management, and complete batch record traceability from raw material receipt to finished product release.
ISO 9001:2015 quality management certification across our manufacturing partner network. Independent annual third-party audits against the full ISO standard. Documented quality objectives, process control measures, corrective and preventive action frameworks, customer complaint management, and continuous improvement protocols — all embedded into day-to-day manufacturing operations, not demonstrated only at audit time.
FSSAI (Food Safety and Standards Authority of India) licensed production and HACCP (Hazard Analysis and Critical Control Points) certified manufacturing for all food supplement and nutraceutical categories. Critical control point monitoring at every production stage with documented corrective action procedures. Complete food safety management system independently verified.
Manufacturing practices aligned to US FDA 21 CFR Part 111 — the Current Good Manufacturing Practice regulations for dietary supplements. Identity testing of all incoming raw materials. In-process quality monitoring. Finished product batch testing against specification. Complete documentation available to support FDA facility inspection and Amazon’s quality documentation requests for US-market supplement brands.
HPLC and UV-Vis spectroscopy verification of active ingredient identity and potency against specification. Every claimed active compound verified at the stated dosage before batch release. No estimate. No assumption. Verified.
Total aerobic count, total yeast and mould count, E. coli, Salmonella, Staphylococcus aureus, and Pseudomonas aeruginosa — all tested to USP and EP limits. Finished product microbiology cleared before any batch receives commercial release authorisation.
ICP-MS analysis for lead, mercury, cadmium, and arsenic against USP and EU maximum limits. Pesticide residue screening using GC-MS and LC-MS/MS for Ayurvedic and herbal-based formulas. Solvent residue testing for extract-based ingredients. Aflatoxin screening for applicable categories.
A Decade of Private Label
Excellence — Measured
in What Matters
Behind every number below is a formulation developed correctly, a batch released only after it passed, and a client brand that trusted us with their name — and came back for their next product. This is what ten years of founder-led, quality-first private label manufacturing in India produces.
Six Reasons Serious Brands
Build Their Private Label
with Jireh
Custom formulation manufacturing is the highest-stakes sourcing decision a supplement brand makes. The wrong partner delays your launch, compromises your formula, or ships product that fails regulatory review in your target market. These six reasons explain why the brands that have done their due diligence end up here — and why they stay for every subsequent product launch.
Our formulation team consists of pharmaceutical scientists with genuine R&D backgrounds — not supplement industry salespeople who know which catalogue numbers to combine. When you brief a formulation requirement, it is evaluated scientifically: clinical literature, bioavailability data, ingredient interaction profiles, and regulatory compliance — before a recommendation is made.
Authentic KSM-66 ashwagandha. Himalayan shilajit. BCM-95 turmeric. These are not ingredients we import — they are ingredients we source from their Indian agricultural origin, verify for botanical authenticity, and extract in our own facility. Your private label formula gets the real thing, at the real source, with full traceability documentation.
Every formulation we develop for a private label client is documented with your name as the proprietary owner. We do not repurpose your ingredient ratios, your stack combinations, or your development findings for another client. Your formula is yours. If you ever choose to manufacture elsewhere, your specification leaves with you. This is not standard practice in our industry. It is standard practice here.
FDA dietary supplement regulations, TGA listed medicine requirements, MHRA food supplement rules, EU permitted ingredient lists, Health Canada NHP regulations — our team navigates all of them. Your formulation is designed to comply from the first draft. Your label is built to the exact specification of your destination market. Your documentation arrives formatted for customs, regulators, and retailer audits.
Nutraceuticals. Pharmaceuticals. Ayurvedics. Peptides. As your private label range grows across product categories, you do not need to source additional manufacturing partners. Our four-facility network covers every major supplement category — each independently GMP-certified, each operating under our unified quality management system. Scale without fragmentation.
Jireh Nutrition Hub is founder-led and founder-accountable. In a manufacturing partnership, that means decisions get made at the right level, problems get escalated and solved directly, and commitments made in a sales conversation are the same commitments honoured in production. A decade of operating this way has produced 200+ active B2B partners — most of whom we never had to acquire twice.
Private Label Manufacturing —
Your Questions
Answered Directly
These are the questions every serious private label client asks before committing to a formulation partner. We have answered them without qualification and without referring you to a brochure — because the brands that ask these questions deserve direct answers. If something is not covered here, our team responds to every enquiry within 24 business hours.
Private label programs begin at 15,000 units per SKU — higher than our white label minimum of 5,000 units, because custom formulation development involves R&D investment that is only commercially viable at higher production volumes. For brands validating a new product concept before committing to a proprietary formula, we typically recommend starting with a white label run to confirm market demand, then transitioning to private label development for the established product.
The complete timeline from initial formulation brief to finished product delivery is typically 12–16 weeks for standard formulations, and 16–20 weeks for complex proprietary blends requiring advanced bioavailability development or novel ingredient combination. This breaks down as: formulation R&D and specification (2–4 weeks), sample production and approval (2–3 weeks), label design and approval (concurrent, 1–2 weeks), full production and QC testing (4–6 weeks), and international shipping (2–4 weeks sea, 5–7 days air).
You own it. Completely and exclusively. Every private label formulation developed for your brand is documented with you as the proprietary specification owner. We do not repurpose your ingredient ratios, your stack combinations, or your development findings for any other client — regardless of whether they operate in the same category. Your formulation specification is delivered to you in full, and if you ever choose to manufacture elsewhere, that specification leaves with you. Full stop.
Yes — and this is often the most efficient development path for private label clients. Our 8,700+ base formulations represent validated starting points. Rather than rebuilding from zero, our scientists can modify an existing formulation to your specification: adding or removing ingredients, adjusting dosages, improving bioavailability, changing the dosage form, or incorporating proprietary botanical combinations. This typically shortens the development timeline and reduces R&D investment compared to a fully ground-up formulation.
Every private label production batch includes a Certificate of Analysis (COA) from an accredited laboratory, Material Safety Data Sheet (MSDS), commercial invoice, packing list, Certificate of Origin, and nutritional analysis. For herbal and botanical formulations, phytosanitary certificates are included as standard. Additional documentation — Country of Pharmaceutical Product (COPP) certificates, organic certificates, halal or kosher certification, regulatory dossiers, and country-specific health certificates — is available based on your destination market requirements.
Yes — sample production and approval is a mandatory stage in our private label development process, not an optional add-on. No full production run begins without your written approval of the physical sample. Samples (50–200 units) are produced from the approved formulation specification, tested for potency and safety, and delivered with a preliminary COA. Sample fees apply for the development and testing investment, but are credited in full against full production orders of 30,000 units and above.
Yes, extensively. A significant portion of our private label clients are Amazon FBA supplement brands or Amazon brand owners expanding into health and wellness. We understand Amazon’s label requirements, FBA packaging specifications, FNSKU barcode placement standards, and the quality documentation Amazon requests during seller verification. We can ship directly to Amazon fulfillment centers in the USA, UK, EU, and Australia with correct shipper labelling, carton marking, and all customs documentation prepared for the destination country.
Our standard private label payment structure is 30% deposit on order confirmation (to begin formulation R&D), 30% upon sample approval and production commencement, and 40% balance before shipment. International payment is accepted via bank wire transfer, Wise, and PayPal. All pricing is quoted in USD with complete line-item transparency — formulation development fees, production costs, testing, packaging, label printing, and logistics all itemised separately with no post-confirmation adjustments or hidden charges.
Ready to Build a Formula
the Market Cannot Copy?
Whether you are building your first proprietary supplement brand, expanding an existing line with a differentiated product, or developing a full multi-SKU wellness range — this conversation is where it starts. Schedule a formulation consultation with our R&D team and receive a complete capability overview, preliminary formulation feasibility assessment, and indicative development pricing within 24 hours.