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5% Minoxidil and Biotin Hair Growth Serum, for restoring thicker hair.

OEM/ODM Private LabelMinoxidil 5% ActiveBiotin Strength ComplexScalp-Nourishing FormulaLow MOQ Support

5% Minoxidil and Biotin Hair Growth Serum, for restoring thicker hair.

Professional-grade Minoxidil 5% and Biotin serum designed for visible hair density restoration and scalp vitality improvement.

Targets thinning and weak hairPromotes stronger, thicker strandsIdeal for daily use
5% Minoxidil and Biotin Hair Growth Serum, for restoring thicker hair.
This 5% Minoxidil Biotin Hair Growth Serum is specially formulated for people with thinning hair and hair loss. It combines the classic hair growth ingredient minoxidil with nourishing biotin, penetrating deep into the scalp and hair roots to help improve the hair follicle growth environment. The serum has a light and refreshing texture, suitable for daily use.
Target Markets Hair care brands, professional salon lines, e-commerce private labels, and men's grooming collections seeking premium hair regrowth solutions.
MOQ 5000 units per SKU, adjustable upon request
Lead Time 30–45 days after sample confirmation
Compliance Can support regional cosmetic GMP and safety documentation as needed
Customization Full formula, packaging, and fragrance customization available upon request

What You Get (One-Stop OEM/ODM)

Formula · Manufacturing · QA · Packaging · Label Support

R&D + Formulation

From fast sampling to iterative optimization—aligned to your market and positioning.

Manufacturing & QC

Stable production workflow with quality checkpoints for consistency and scale-up.

Packaging & Launch Support

Packaging options, decoration, labeling/INCI coordination—helping you launch shelf-ready SKUs.

Product Fit

Skin Type & Key Benefits
All scalp typesOily scalpDry scalpSensitive scalp

1、Applicability

thinning hair, hair loss, weak roots, daily use, all scalp types

2、Main Functions

stimulates hair growth, nourishes follicles, strengthens roots, improves scalp health, enhances density

3、Suitable Population

Men and women experiencing thinning hair, postpartum shedding, or early-stage hair loss.

Formula Customization Options

What you can change (and how far).
A
Active Ingredient LevelAdjust Minoxidil concentration or supplement with herbal actives upon requirement.
F
Fragrance and TextureOptions for unscented, mild herb, or refreshing fragrance based on target market.
B
Bottle DesignCustom dropper, spray, or pump bottle with private labeling.
O
Outer PackagingBox, labeling, and printing materials tailored for retail display.
V
Volume OptionsCommon sizes include 30ml, 50ml, or 100ml; custom volumes supported.
F
Formula ClaimsCan support anti-hair loss, thickening, or scalp-balancing claims per your positioning.
R
Raw Material BrandingIngredient branding and botanical source certificate options available upon request.

Packaging & Craftsmanship

We can supply shelf-ready, retail-ready SKUs.

Packaging Options

Amber glass bottle with dropperHDPE opaque pump bottlePET clear bottle with fine mist sprayerCustom bottle shape mouldTravel-size mini packaging

Decoration & Finishing

Silkscreen printingHot stampingLabel appliqueMatte or glossy coatingEmbossed logo
Recommended Packaging Direction
Opt for opaque bottles to minimize light exposure and maintain Minoxidil stability.
Ask for Packaging Options

MOQ & Lead Time

MOQ
MOQ flexible for initial market testing; bulk price tiers available.
Sampling
Sample preparation typically within 5–7 working days. (1–3 formula options)
Bulk Production
Mass production lead time about 30–45 days post sample approval. after final approval
OEM Scope
Full OEM/ODM cooperation including formula development, packaging design, filling, and regulatory filing support where applicable.
Incoterms: FOB Guangzhou or EXW terms; other terms available upon request. Shelf-life: 24 months under normal storage conditions.

Testing & Documents (Available)

Stability Testing

Ensures long-term ingredient and color stability under various temperatures.

Dermatological Safety

Formulated to minimize scalp irritation; patch test recommended.

Efficacy Evaluation

Custom efficacy test protocols can be arranged to validate hair density performance.

Buyer-ready checklist
Request the document set you need for your region.
Email our team
How do you accelerate sampling and reach a golden sample faster for EU buyers?

As your OEM partner, we accelerate sampling by starting with a pre-approved hair care formula base from our library, tailored to EU regulations like REACH and SCCS. This cuts R&D time by up to 2 weeks. We run stability, microbiological, and packaging compatibility tests in parallel during sample production, not sequentially. For EU buyers, we immediately align on critical specs: claims boundaries, ingredient restrictions, and label requirements to avoid rework. Packaging is sourced from pre-tooled components or rapid prototyping to fit samples quickly. We provide documentation support including CPSRs and test reports, but final regulatory approval is your responsibility as the brand owner. The golden sample process typically takes 3-4 weeks with expedited options, versus 6-8 weeks standard. Key drivers: clear briefs, using existing molds, and upfront compliance checks. We recommend a pilot batch of 500-1000 units post-sample to validate scale-up before full production.

How do European buyers compare hair care suppliers: EU compliance support, QA, and consistency?

European buyers compare hair care suppliers by first assessing EU compliance support. They look for suppliers who can assist with safety assessments, product information files (PIF), and testing for heavy metals, allergens, and microbial limits under Regulation 1223/2009. This includes documentation management and guidance on labeling requirements. For QA and consistency, buyers review the supplier's quality systems, such as in-house microbiology labs, stability testing, and batch uniformity checks for viscosity, pH, and performance. Consistency is ensured through standardized production and regular audits. Concrete details: MOQ guidance typically starts at 5,000 units for shampoos and conditioners. Sampling timeline is 2-4 weeks for formula approval. Lead time from production to shipping is 8-12 weeks, depending on packaging complexity. Packaging must comply with EU labeling, including INCI lists and multilingual options. We support all necessary testing and documentation but cannot guarantee regulatory approval; buyers should verify with local authorities.

What information should EU buyers include in an RFQ to get an accurate hair care quote?

To get an accurate hair care quote for the EU market, include your target channels like Amazon, retail, or salons, and list all SKUs with formats such as shampoo, conditioner, or mask and sizes like 200ml or 500ml. Specify packaging materials and designs, noting if you need sustainable options like PCR plastic or refillable systems, as EU compliance requires specific labeling and material safety. Also, outline any claims like sulfate-free or color-safe, as we can help ensure they meet EU Regulation (EC) No 1223/2009 through documentation and testing. Provide your budget per unit and launch timeline to align production. MOQs typically start at 3,000-5,000 units per SKU but drop with higher volumes or simpler packaging. Sampling takes 4-6 weeks with stability and compatibility checks, while full production lead time is 8-12 weeks post-approval, including CPNP notification and safety assessment support.

How do you formulate a scalp serum for oily scalp without irritation risk?

To formulate a scalp serum for oily scalp without irritation, we focus on lightweight, non-comedogenic bases such as hyaluronic acid or squalane, and incorporate actives like zinc PCA for sebum regulation and prebiotics for microbiome balance. We exclude potential irritants like alcohol denat or fragrances, and conduct patch testing during R&D to minimize risk. For sampling, we offer lab samples within 2-3 weeks, with MOQs typically starting at 10,000-20,000 units per SKU depending on packaging complexity. Common packaging includes airless pumps or dropper bottles to prevent contamination and ensure precise application. Testing involves microbial analysis, stability studies under EU storage conditions, and compatibility checks with packaging materials. We support documentation like the Product Information File (PIF) and safety assessments, but do not guarantee regulatory approval. Lead time from final sample approval to production is 8-12 weeks, factoring in raw material sourcing and quality control stages. Our GMP-certified facility ensures consistent batch quality for EU market entry.

How do you formulate an anti-dandruff positioning shampoo without making drug claims in the EU?

In the EU, anti-dandruff shampoos must be positioned as cosmetics, not drugs, by focusing on cosmetic claims like 'helps reduce visible flakes' and using approved ingredients such as piroctone olamine or climbazole, while avoiding banned substances like zinc pyrithione in certain concentrations. Key details include MOQ guidance of 10,000 units minimum, which can drop to 5,000 for stock packaging, and a sampling timeline of 3-4 weeks after formula approval, including stability checks for viscosity and pH under varied temperatures. For testing and docs, we conduct microbial hold-time tests, provide a Product Information File (PIF) with safety assessments, and ensure packaging labels meet EU regulation (EC) No 1223/2009 with ingredient lists in local languages. Lead time from production to shipping is 8-12 weeks, factoring in batch QA for leakage risks and pigment dispersion in final mixes. We avoid guaranteeing regulatory approval but assist with all necessary compliance steps to streamline your launch.

How do you set shelf life and PAO for hair care under EU expectations?

In the EU, shelf life and Period After Opening (PAO) for hair care products are established based on EU Cosmetics Regulation (EC) No 1223/2009, which requires evidence of product stability over time. We conduct accelerated stability testing at elevated temperatures (e.g., 40°C for 3 months) and real-time testing under normal conditions to determine expiration dates and recommend PAO symbols (like 6M or 12M) based on formulation type and packaging. For MOQ guidance, minimum order quantities of 5,000-10,000 units often justify the cost of full stability studies, with smaller batches relying on accelerated data but requiring longer lead times. Sampling timelines typically involve 4-6 weeks for initial stability checks, followed by 3-6 months for complete testing cycles, depending on product complexity (e.g., shampoos vs. serums). Testing and documentation include stability reports, microbial challenge tests to assess preservative efficacy, and compatibility tests with packaging materials to prevent leaching or degradation. We assist in preparing all necessary documents, such as Product Information Files (PIFs) and safety assessments, for EU market entry, though final regulatory approval is the brand's responsibility. Packaging choices, like airless pumps or UV-protected bottles, can extend shelf life by reducing oxidation, and we optimize production lead times to 8-12 weeks from final approval to shipping, incorporating QA checkpoints for batch consistency.

What should a real COA include for shampoo, conditioner, hair mask, and scalp serum?

A Certificate of Analysis (COA) is a mandatory quality document for hair care products like shampoo, conditioner, hair mask, and scalp serum in the EU. It confirms each batch meets specified standards under EU Regulation EC No 1223/2009, ensuring traceability and safety for consumers. Without a proper COA, products cannot be legally sold or imported into the EU market, risking non-compliance penalties or recalls. Key inclusions are product name and code, batch number, production and expiry dates, manufacturer details, and test parameters with acceptance limits. For hair care, typical tests cover pH (4.0-7.0 for most), viscosity, microbial limits (e.g., <100 CFU/g for bacteria), heavy metals (lead, arsenic), preservative efficacy, and stability data under accelerated conditions. The COA must also state compliance with EU cosmetic product safety reports and ingredient restrictions, such as banned substances or allergen labeling. From a factory perspective, generating a COA involves batch-specific testing after production, which adds 1-2 weeks to lead time depending on lab capacity. MOQ influences this: smaller batches may have higher per-unit testing costs, while larger batches ensure consistency and cost efficiency. Sampling for COA requires pilot batches to validate formulations, with timelines of 3-4 weeks for testing and documentation. Packaging must be validated for compatibility to prevent leaching or contamination, affecting COA stability claims. We support by conducting in-house or third-party tests, providing draft COAs for review, and assisting with documentation for EU notifications, but final regulatory approval depends on authorities. Always factor in COA preparation when planning launch dates to avoid delays.

What is the EU compliance-ready document pack for private label hair care shipments?

For EU shipments of private label hair care, the compliance document pack must meet Regulation (EC) No 1223/2009. Key elements are the Product Information File (PIF) with a safety assessment by an expert, detailed formula with ingredient concentrations, and proof for claims like 'volumizing' or 'repair'. We start this during sampling, which takes 2-3 weeks after formula approval, and MOQ guidance is typically 5,000 units per SKU to justify documentation costs. Testing includes microbiological, stability, and packaging compatibility checks to ensure safety and prevent leakage. Packaging must have EU-compliant labels with INCI ingredient lists in the target country's language, and we provide GMP certificates. Lead time from order to shipment is 8-10 weeks, including 2 weeks for document compilation. We support with all tests and documentation, but brands must verify final compliance with local authorities. For efficiency, we recommend batching orders to optimize MOQ and reduce lead time variations, and our QA team aligns in-process checks with documentation.

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Send target market + MOQ + packaging preference to get a fast quote.
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Typical Sampling Process (B2B / OEM)

1
Submit RequirementsShare target function, fragrance, and packaging preferences.
2
Formula ProposalOur lab will propose a suitable formulation based on your brief.
3
Sample PreparationLab samples are produced within approximately 5–7 days.
4
Client EvaluationYou review and feedback on appearance, texture, and efficacy.
5
Adjustment & ConfirmationFormula revised as needed until approval.
6
Packaging FinalizationFinalize bottle and decoration designs for mass production.
7
Production Kick-offBegin full-scale production and packing after deposit and sample confirmation.
  • Our team will answer your inquiries within 8 hours.
  • Your information will be kept strictly confidential.

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