INTRODUCING OUR NEW SERVICE: Private Label (Eom)

Empower Your Brand with Scientifically Backed, FDA-Compliant Custom Formulations

With 28 years of expertise in advanced R&D, clinical-grade formulation, and GMP-compliant manufacturing in the United States, we are proud to launch our Private Label (EOM – Exclusive Original Manufacturing) service — a complete, professional solution for individuals, clinics, spas, and distributors seeking to launch their own branded product lines with regulatory peace of mind and scientific credibility.

Two Flexible Pathways To Build Your Brand

FREQUENTLY ASKED QUESTIONS (FAQ)

  1. I don’t have a formula yet. Can you help develop one?

Absolutely. With nearly three decades of experience in product R&D, our formulation scientists will work with you to create a safe, evidence-based product that meets your functional, aesthetic, and commercial goals.

  1. Will my formula be protected and kept confidential?

Yes. We sign a Non-Disclosure Agreement (NDA) with every OEM client. Your proprietary formulations, concepts, and intellectual property are protected at the highest legal and professional level.

  1. Can I just choose a pre-formulated product and rebrand it?

Yes. Our White Label offering allows you to choose from a wide range of proven, lab-tested products. You can customize the packaging and brand identity, and we’ll ensure compliance with FDA labeling standards.

  1. What is the minimum order quantity (MOQ)?

Cosmetic and peptide-based products: from 100–500 units

Nutritional supplements and injectables: from 1,000 units

We will advise you on the most cost-effective pathway for your specific product category and business model.

  1. Are your ingredients certified and traceable?

Yes. All raw materials are sourced from FDA-compliant, GMP-certified, and safety-tested suppliers. We provide full documentation, including COA (Certificate of Analysis), MSDS, origin traceability, and storage protocols.

  1. Can I sell the product internationally?

Yes. We offer support for export documentation, international registrations, and compliance standards for markets such as the EU, Canada, Vietnam, the Middle East, and more.

  1. What other support do you provide beyond manufacturing?

Our value-added services include:

  • Formula review and safety assessment
  • Clinical guidance for skin health and wellness use cases (at no cost)
  • FDA-compliant content creation and product labeling
  • Packaging design and marketing consulting
  • Long-term product development strategy support
  1. How long does it take to complete a Private Label order?

Lead times vary depending on the product category, complexity of the formulation, and raw material sourcing. On average, projects take 6–8 weeks from the time the formula and packaging are approved. For products requiring specialty ingredients or advanced testing, timelines may be extended slightly to ensure quality and compliance.

  1. Do you handle product stability and safety testing?

Yes. All products undergo safety verification and, where applicable, stability testing in compliance with FDA and international regulatory standards. This ensures your product remains safe, effective, and market-ready throughout its intended shelf life.

  1. Can you help with packaging design and FDA-compliant labeling?

Absolutely. Our creative and regulatory teams work together to deliver packaging that is both visually compelling and fully compliant with FDA requirements, covering ingredient listings, claims, and usage instructions.

  1. Do you provide market or clinical guidance on product selection?

Yes – at no cost. With 28 years of industry expertise, we offer complimentary consultations to help you select or develop products that are scientifically sound, commercially viable, and aligned with current market trends in aesthetics, skin health, and wellness.