Beyond Basix NAD+ Peptide Clinic & Spa OEM Serum — Custom Formulations

Beyond Basix NAD+ Peptide Clinic & Spa OEM Serum is a professional-grade, customizable treatment serum that combines NAD+ precursors and targeted peptides to support cellular energy, skin repair, collagen synthesis, and visible anti-aging results. Designed specifically for professional use in clinics and spas, our formulations prioritize fast absorption, clinical tolerability, and synergistic ingredient profiles that enhance treatment outcomes. Backed by Guangzhou Beyond Basix Cosmetics Ltd.’s 23 years of R&D and manufacturing experience and produced in a 100,000-level GMPC pharmaceutical-grade workshop, our NAD+ peptide solutions deliver both efficacy and manufacturing quality you can trust. (Keyword: nad+ peptide oem for clinics and spas)

Yes — we provide full OEM/ODM custom formulation and private-label services. The typical process: 1) Discovery call to define objectives, target skin concerns, regulatory markets and packaging; 2) NDA and formulation proposal; 3) R&D and prototype (adjustable concentrations, peptide selection, carriers); 4) Stability, microbial and compatibility testing; 5) Samples for clinical or in-house evaluation; 6) Packaging design and production; 7) Mass manufacturing and delivery. Timelines vary by complexity, but most custom prototypes take 2–6 weeks and full stability/production runs 8–14 weeks. Our 12 production lines and advanced equipment let us scale from small boutique orders to large clinic chains efficiently. We also support label artwork, claims review and multilingual packaging.

Quality and safety are core to our manufacturing. Guangzhou Beyond Basix operates a 12,000 m² facility with a 100,000-level GMPC workshop, 12 production lines and advanced equipment from Germany and the US. We are certified to ISO 9001 and GMP and maintain CE, MSDS, HALAL and other certifications as required. Every batch undergoes raw material traceability, microbial testing, preservative efficacy, heavy metal and stability testing, and Certificate of Analysis (COA) documentation. We can also arrange third-party testing or clinical evaluations to support market entry and comply with local regulations. This rigorous approach ensures products are safe, stable and market-ready.

MOQs depend on packaging format and customization level. Typical MOQs range from small trial runs (100–500 units) for sample or pilot orders up to standard commercial MOQs of 1,000+ units. Pricing is influenced by active concentrations (NAD+ precursors and peptide complexity), raw material grade, packaging choice (airless pump, glass dropper, etc.), and regulatory/testing requirements. Estimated lead times: prototype 2–6 weeks, stability and regulatory checks 4–8 weeks, and mass production 4–10 weeks after approval. For an accurate quote and optimized MOQ, provide target formulation, packaging, and annual volume and we will prepare a tailored proposal.

Yes. We provide comprehensive post-manufacturing support including ingredient and efficacy dossiers, COAs, MSDS, stability reports, and production batch records. For stronger market positioning, we can assist with claim substantiation strategies, arrange clinical or consumer studies, produce before/after imagery protocols, and supply technical copy and multilingual labels tailored to clinic and spa settings. Leveraging our experience developing four brands (LANTHOME, PANSLY, FIRSTSUN, SAUVASINE) and 12 years focused on potent skincare actives, we help partners create credible, compliant marketing that highlights the performance of nad+ peptide oem for clinics and spas while meeting regulatory standards.