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Hair Care OEM/ODM FAQs (MOQ, Samples, Packaging & QA)

This Hair Care FAQ hub helps buyers spec and de-risk shampoo, conditioner, masks, scalp care, and leave-ins—before placing a PO. Browse questions by stage (Start, Sampling, Production, Shipping) and topic (MOQ & cost, packaging fit, testing & QA, compliance docs, lead time) to get RFQ-ready faster.

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Where relevant, we reference audit-ready evidence (certs, compliance files, and test reports) so procurement and QA teams can speed up supplier due diligence.

European buyers for private label hair care products commonly require specific documents for regulatory compliance and quality assurance. The Certificate of Analysis (COA) confirms each batch meets ingredient and performance specifications. The Safety Data Sheet (SDS) is mandatory under EU CLP regulations for safe handling and transport. Stability test reports, often covering 3-6 months under […]

Our fragrance control starts with GC-MS fingerprinting of every fragrance batch before production. We maintain a master reference profile for each scent and compare every incoming batch against this standard. For hair care formulations, we blend fragrances in temperature-controlled rooms (22±2°C) with automated mixing to ensure uniform dispersion. Each production batch undergoes headspace GC analysis […]

For US market compliance, we commonly formulate with pyrithione zinc (0.3-1%), selenium sulfide (1%), salicylic acid (1.8-3%), ketoconazole (1%), and coal tar (0.5-5%). Our MOQ starts at 3,000 units for standard formats. Sampling takes 4-6 weeks including stability testing. We provide full documentation including ingredient specifications and safety data. Packaging must consider active compatibility with […]

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