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Private Label & OEM/ODM Cosmetics Manufacturing FAQs

Welcome to LAEYO’s manufacturing FAQ hub. Here you’ll find practical answers to the questions buyers ask most—MOQ, sampling time, custom formulation, compliance documents, packaging, lead time, and U.S. shipping/Amazon FBA requirements. Start by browsing by product category or search for your topic, then share your target market and SKU plan to get an accurate quote.

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Browse FAQs by Product Category

To help you find the answers you need quickly and easily, we’ve organized our FAQs into the categories below. If you need further assistance, feel free to contact us anytime.

Body Care FAQs

This Body Care FAQ hub answers the questions buyers ask most—MOQ and sampling, lead time planning, fragrance direction (or fragrance-free), packaging compatibility (pumps/foamers), testing scope, and compliance documents. Use these FAQs to shortlist SKUs and align requirements before you request an RFQ.

Eye Care FAQs

This Eye Care FAQ hub answers the questions buyers ask most—MOQ and sampling, lead time planning, packaging compatibility (airless pumps, tubes, jars), testing scope (stability/micro), and compliance documents. Use these FAQs to align requirements, shortlist candidates, and move faster from samples to RFQ.

Fragrance OEM/ODM FAQs

Perfume buyers ask different questions than skincare—IFRA/allergens, alcohol vs oil formats, leakage risk (bottle/atomizer/crimp), and hazardous shipping paperwork. This FAQ hub covers MOQ, sampling, concentration choices (EDP/EDT/extrait), documentation (SDS/MSDS), packaging checks, and shipping planning so you can align specs before requesting an RFQ.

Hair Care FAQs

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.

Lip Care FAQs

This Lip Care FAQ hub covers what buyers ask most—MOQ and sampling, taste/odor expectations, glide and finish targets, packaging compatibility (tube/jar/applicator), and leakage risk in transit. Use these FAQs to align specs fast, shortlist sample SKUs, and reduce rework before you request an RFQ.

Men Care FAQs

Typical buyer questions for men care: performance specs, scent direction, and packaging durability—especially for Amazon/FBA and barbershop channels. Use these FAQs to lock specs for repeat orders, shortlist sample-ready SKUs, and reduce leakage/breakage risk before you request an RFQ.

Mom & Baby Care FAQs

This Mom & Baby Care FAQ hub answers the questions buyers ask most—MOQ and sampling timelines, fragrance-free policy, mildness targets, safe packaging/closures, testing scope, and compliance documents. Use these FAQs to align requirements and shortlist options before you request samples or send an RFQ.

Skincare OEM/ODM FAQs

Start here if you’re sourcing skincare for DTC, Amazon/FBA, retail, or distributors. These FAQs focus on what actually determines feasibility and rework risk: MOQ drivers (formula vs packaging), sampling steps (3–7 days + 1–2 iterations), claims boundaries, stability/compatibility checks, and packaging fit (pump, tube, airless). Need audit-ready proof? Use our Trust Center to request the right compliance pack (SDS/MSDS, COA, INCI) and certifications for your target market.

Sunscreen OEM/ODM FAQs

This Sunscreen FAQ hub covers the questions buyers ask before committing to samples—SPF/UVA targets, water resistance, white-cast control, testing scope, and packaging compatibility (spray valves, leakage control, label durability). Use these answers to align target market requirements and packaging direction first, then request samples or submit an RFQ with fewer back-and-forths.

Most Asked Questions (Start Here)

These are the questions that decide feasibility, timeline, and rework risk. Expand to read the answer.

To prevent leakage in beard oil droppers and pump bottles during shipping, we implement a multi-step quality assurance protocol starting from design to final packaging. This includes pressure testing each batch to simulate air freight altitude changes and seal integrity checks for dropper caps and pump mechanisms, ensuring they can handle temperature shifts during transit. We also use torque testing for pump bottles to verify closure tightness and conduct fill-level audits to avoid overfilling, which reduces leakage risks from product expansion. For sampling, we recommend a 2-3 week timeline to test prototypes under real shipping conditions, with MOQ guidance typically starting at 5,000 units per SKU to justify custom tooling for secure seals. During production, we perform leakage tests at different temperatures to account for oil viscosity variations and use secure secondary packaging like foam inserts to minimize movement. Lead time from order to shipping is 6-8 weeks, including time for these QA steps and compliance documentation. For the US market, we support documentation such as FDA facility registration and product safety testing reports, but final regulatory approval remains the brand's responsibility. We ensure all packaging meets standard drop-test requirements and provide certificates of analysis for traceability.

Sample development for men care products, such as shaving creams or beard oils, usually takes 2 to 4 weeks from initial brief to sample delivery. This timeline can vary based on factors like formulation complexity, raw material availability, and packaging customization needs. For instance, custom pump or bottle tooling can add 1-2 weeks, while stability testing for active ingredients may require additional time. Key drivers include: formulation stability and microbial testing, which are critical for US FDA compliance; packaging fit and leakage prevention checks, especially for airless pumps or sprays; and documentation support for ingredient safety assessments. We recommend sharing detailed specs early, including target cost, SKU size, and market claims, to avoid delays. At LAEYO Labs, we guide on sample MOQ (typically 50-100 units) and lead time gates. Post-sample approval, production lead time is 4-6 weeks, depending on order volume and packaging sourcing. We assist with testing protocols and compliance docs, but do not guarantee regulatory approval—brands should plan for extra time for third-party certifications or label reviews.

Packaging compatibility testing is a quality assurance process that evaluates how packaging components, such as bottles, caps, or tubes, interact with men's care products like shaving gels, beard oils, or face washes. This testing checks for chemical migration, physical changes, seal integrity, and stability under various conditions to prevent product degradation, discoloration, or safety risks. For the US market, it's crucial to align with FDA guidelines and industry standards like CTFA, ensuring consumer safety and compliance. The ideal timing is during the sampling stage after finalizing packaging design but before pilot production; this allows for adjustments if tests reveal incompatibilities, avoiding costly delays or recalls later. From an OEM/ODM perspective, factors like MOQ (Minimum Order Quantity) influence testing scope—for instance, MOQs starting from 3,000 to 5,000 units may include basic compatibility tests in sampling fees, while higher volumes require more comprehensive checks. Sampling timelines typically take 2 to 4 weeks for compatibility testing, depending on the product type and packaging complexity. Required documents include test reports, material safety data sheets (MSDS), and certificates of analysis, which we support by facilitating third-party lab testing if needed. Packaging choices, such as PET bottles for liquids or airless pumps for creams, must be validated through accelerated stability tests that simulate shelf life and storage conditions. Lead times for production can extend by 1 to 3 weeks if testing identifies issues, so early planning is essential to meet launch dates. We assist buyers by providing documentation support and testing coordination to streamline US market entry, focusing on practical steps like pre-shipment inspections and humidity resistance checks for reliable outcomes.

As a manufacturer, we recommend auditing at raw material receipt, in-process blending, filling, and final packaging. Key checkpoints include verifying COAs for active ingredients, monitoring viscosity and pH during mixing to ensure consistency, and conducting fill weight checks to prevent underfills. For the US market, microbial testing at critical stages is essential to meet FDA guidelines. Sampling typically takes 3-4 weeks after MOQ confirmation, with pilot batches used for stability testing. Packaging audits should focus on label alignment, pump torque consistency, and leakage tests under simulated shipping conditions. We provide all necessary documentation, including batch records and test reports, to support your regulatory submissions. Lead time from production start to shipping is 6-8 weeks, depending on MOQ and complexity. We advise on MOQ based on your sales forecast to optimize costs. Our QA team ensures every batch meets your specifications and compliance requirements. For specific products like beard oils, check essential oil dispersion and oxidation stability; for shaving creams, test foam density and canister pressure integrity.

Pomade is typically oil- or water-based, delivering high shine and flexibility for classic styles; clay provides a matte finish and firm hold, ideal for textured looks; wax offers medium hold with a semi-matte sheen for definition; and paste is versatile with moderate hold and finish, suited for daily use. Buyers should consider hair texture (fine, thick, curly), desired effect (natural, sleek, messy), and hold duration (light, medium, strong) to match their brand positioning and customer needs. For OEM/ODM production, MOQ for men styling products ranges 3,000-5,000 units per SKU, driven by packaging costs and raw material batches. Sampling takes 2-4 weeks for lab samples and 4-6 weeks for pilot batches, with viscosity and hold testing to ensure consistency. We support FDA compliance for the US market, including ingredient safety reviews, label approvals, and microbial stability checks over 3 months. Packaging options include jars, tubes, or pumps; we conduct leakage tests simulating air-freight pressure changes and humidity cycles to prevent failures. Lead time is 8-12 weeks from order to shipment, with gates for QA checks like fill weight, torque testing for caps, and pigment dispersion. Documentation includes COA, SDS, and batch records for audit trails.

To pass microbiology on sunscreen, we start from formula design: water phase load, pH, and your UV filters/emulsifiers can weaken certain preservatives. We typically shortlist 2-3 systems, then stress them in our microbiology challenge room and check compatibility (odor, viscosity drift, separation) with your target packaging. For the US, we align the preservative choice with your brand's compliance strategy (OTC sunscreen expectations, retailer/Amazon requirements) and can support the test package: micro limits, preservative efficacy (challenge) test, stability, and full batch documentation. Our factory runs under ISO 9001:2015 and we can provide REACH-related documentation where relevant. Commercially, MOQ is usually driven by packaging supplier minimums; we confirm after you pick the pack (e.g., tube lead time about 15 working days; acrylic bottle about 30). After sample sign-off, bulk production is commonly 10-20 working days, and an end-to-end one-stop launch typically lands in 45-60 days depending on packaging and testing scheduling.

For the US market, our private label MOQ is generally 1,000-3,000 pcs per SKU (each SKU = one formula + one packaging format). Simple, straightforward processes can start at 1,000 pcs (for example, sheet masks). If you are launching a skincare set/kit with more complex packaging, multiple items, or higher formulation/packaging complexity, the MOQ typically moves to 3,000 pcs. We support formula customization and lab sampling so you can confirm texture, fragrance, and performance before mass production. After sample approval, bulk production is usually 10-20 working days. Packaging ordering commonly takes 10-30 working days, so aligning artwork and packaging specs early helps keep timelines predictable. Packaging lead times (typical): inner packaging glass bottle ~15 days, acrylic bottle ~30 days, tube ~15 days, mask pouch ~15 days; outer packaging single box ~15 days, set box ~20 days. We can support documentation and product testing/inspection workflows (including tracking test reports), plus design and logistics coordination, but we do not guarantee regulatory approvals.

For a private label shampoo, we can usually deliver pre-production samples in about 10-20 working days once we lock the formula direction (scent, texture, key ingredients) and confirm what you want in the sample (bulk only vs filled + labeled). Our standard flow is: product selection,方案确认, contract, brand/pack design, then sample confirmation before mass production. Timing depends on materials and checks: raw material production is typically 5-7 working days, raw material testing about 5 working days, and finished-goods manufacturing steps are commonly around 7 working days. If you need packaging involved, packaging can be the long pole: inner pack examples include glass bottles 15 working days or acrylic bottles 30 working days; outer cartons are typically 15 working days (single box) or 20 working days (set box). Packaging testing can take about 3 days. For MOQ guidance, most items start at 1000-3000 units (simpler processes lower; more complex packs/formulas higher). After sample approval, bulk production delivery is commonly 10-20 working days, and we can support documentation and third-party testing/inspection coordination for US market needs.

In the US, hair growth/loss claims fall under FDA's drug classification, requiring extensive safety and efficacy data. We recommend using structure/function claims like 'supports healthy hair' instead. For drug claims, expect 6-9 months for testing and $15k-25k in documentation costs. Our MOQ for compliant formulations is 5,000 units. Sampling takes 4-6 weeks with stability testing. Packaging must include proper warnings and disclaimers. Lead time extends to 12-16 weeks for compliant products. We can support documentation but cannot guarantee FDA approval.

For US market lip care, shrink bands are most cost-effective with 5,000-unit MOQs, while induction seals require 10,000+ units due to specialized equipment needs. Custom tamper-evident designs start at 15,000 units. Sampling takes 2-3 weeks for prototype testing, including 72-hour humidity exposure checks. We provide ISO 22716-compliant documentation and can support FDA registration support. Lead time extends by 7-10 days for tamper-evident integration. Air freight pressure testing is included to prevent leakage during transit.

Tip: The search + filters above also work on these Q&A blocks. Type a keyword (e.g., “leakage”, “Alcohol-free”, “SPF”) to narrow instantly.

Send a Faster RFQ (Copy & Paste Checklist)

Copy the checklist, fill it in, and send it to speed up feasibility + next steps.

Target market & channel:
Product list (SKUs + format):
Positioning & claims direction:
Packaging preference (bottle/jar/tube + closure):
Target price band:
Quantity plan (pilot / first PO / 6-month forecast):
Required documents (COA/MSDS/SDS, IFRA, SPF route, etc.):
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