Premium Cosmeceutical Manufacturing.
End-to-end custom formulation and private-label production with specification-led development, packaging support, and selected starting MOQs from 500–1000 pc.
Engineered for Active Stability & Sensory Excellence
Explore seven specialized formulation suites engineered for active stability, sensory excellence, and regulatory compliance.
Advanced Skin Care
Clinical serums, barrier repair creams, treatments & gentle cleansers.
Explore Formulation Suite
Scalp & Hair Therapeutics
Sulphate-free shampoos, peptide scalp serums & botanical oils.
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Body & Dermal Wellness
Niacinamide body lotions, AHA body scrubs & rich botanical wraps.
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Pediatric & Maternity Care
Hypoallergenic, tear-free pediatric & maternity barrier treatments.
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Men's Grooming & Performance
Matte-finish face moisturizers, beard growth serums & post-shave gels.
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Suncare & Personal Hygiene
Broad-spectrum SPF 50 sunscreens, roll-on deodorants & intimate washes.
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Curated Bundles & Travel Sets
Custom packaged retail discovery sets & seasonal gifting collections.
Explore Formulation SuiteTurnkey Cosmeceutical Manufacturing Pipeline
End-to-end OEM/ODM capabilities spanning active bio-sourcing, vacuum homogenisation, stability testing, and custom packaging.
Turnkey Private Label Manufacturing
Turnkey contract manufacturing for beauty and wellness brands, spanning ingredient sourcing, controlled processing, filling, secondary packaging, and the applicable product documentation.
Custom Formula Scale-Up & Toll Manufacturing
Seamless scale-up of your proprietary formulations from bench-top samples to multi-ton production batches. Equipped with vacuum homogenizers delivering 0.2–5 micron micro-droplet stability.
Bio-Active Cosmeceutical R&D
Custom formulation development for high-efficacy treatments: multi-weight Hyaluronic Acid complexes, micro-encapsulated Retinoids, Niacinamide barrier gels, and lipid-replenishing Ceramide matrices aligned to pH 4.5–5.5 skin mantles.
Primary & Secondary Packaging Integration
Comprehensive packaging solutions tailored to active ingredient stability. Includes airless bottles to prevent active oxidation, UV-blocking amber dropper bottles, barrier laminate tubes, and eco-conscious PCR plastics.
Analytical QC & ICH Stability Testing
Quality plans are agreed against the product specification and intended market. They can include pH, viscosity, microbial-limit, stability, compatibility, or other product-specific checks, with release documentation defined before production.
Indian & International Regulatory Documentation
Documentation support can cover INCI ingredient lists, agreed testing records, label review, and market-specific files for domestic or export readiness. The exact scope is confirmed for each product and destination.
Production Lead-Time & Specification Estimator
Select your target batch quantity to evaluate production lead-times, sampling turnarounds, QC protocols, and packaging compatibility.
Regulatory Dossiers & Bio-Active Standards
Review our compliance frameworks and proven active carrier compatibility matrix.
Licensing & Label Support
Support for applicable Indian cosmetic licensing, ingredient declarations, label review, and product documentation is scoped against the product category and route to market.
Quality-Managed Manufacturing
GMP-aligned production controls, documented cleaning and batch procedures, in-process checks, and defined release specifications support repeatable manufacturing.
Agreed Stability Programme
Stability work is scoped to the formulation, packaging system, target shelf life, and destination-market requirements before commercial production.
Market-Ready Documentation
Support can include standardized INCI declarations and the agreed product, packaging, and testing records for the intended domestic or export market.
From Technical Brief to Retail-Ready Dispatch
A transparent five-phase pathway with development, production, testing, packaging, and dispatch timelines confirmed against the approved scope.
Brief & Target Active Mapping
Define target consumer, preferred benchmark product, active percentage requirements, and benchmark budget. An initial technical review follows before sampling begins.
Lab Formulation & Sample Dispatch
Our R&D chemists prepare bench-top samples and refine viscosity, skin feel, fragrance direction, and other agreed attributes until the client approves the development sample.
Costing, Packaging & Documentation Review
Transparent itemized quotation per unit, final MOQ confirmation, packaging compatibility checks, and review of the applicable regulatory documentation.
Controlled Batch Production & QC
Controlled mixing and homogenization are followed by the agreed pH, viscosity, microbial-limit, and release checks for the formulation.
Inline Filling, Labelling & CoA Dispatch
Automatic filling under laminar airflow, precision batch coding, shrink wrapping, and shipping with Certificate of Analysis (CoA) and batch manufacturing records.
Frequently Asked Questions
What are your Minimum Order Quantities (MOQs)?
Our MOQ starts at just 500–1000 pc per SKU for standard stock packaging, making it ideal for emerging D2C beauty brands testing new formulations. For custom packaging componentry or bespoke molded jars, MOQs typically start at 2,500–5,000 units.
Can you manufacture formulations using our custom active ingredients?
Yes. We accept client-supplied proprietary ingredients (such as patented botanical extracts or specialized peptide complexes) subject to safety data sheet (SDS) review and lab compatibility testing.
What quality control testing is performed on each batch?
Every production batch undergoes analytical testing in our QC lab: pH balance verification, viscosity measurement, specific gravity, organoleptic testing, and microbial limit testing (Total Viable Count, Yeast & Mold). A signed Certificate of Analysis (CoA) accompanies every dispatch.
Do you provide regulatory licensing support for selling in India and exporting?
Yes. Support can include applicable Indian cosmetic licensing documentation, product label and INCI review, and agreed export documentation for markets such as the United States or European Union. The exact scope is confirmed for each product and destination market.
How long does formulation sampling and mass production take?
Our target turnaround for an approved formulation brief is within 14 business days for the first R&D sample. Once you approve the sample, mass batch production and inline filling typically require 18–21 business days, depending on packaging component lead times.
Can you handle custom primary and secondary packaging?
Yes. We work with airless pump bottles, glass droppers, aluminium tubes, PCR plastic bottles, and luxury unit cartons. We also offer screen printing, hot foil stamping, and pressure-sensitive labelling.
Ready to Formulate Your Next Hero Product?
Share your intended product, benchmark, packaging direction, target market, and batch quantity for a structured technical review.
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