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Peach exfoliating foot scrub mask

OEM/ODM AvailableSmall Batch CustomizationFast SamplingRich Formula LibraryPrivate Label Support

Peach exfoliating foot scrub mask

Revitalize tired feet with gentle peach exfoliation and nourishing care — perfect for professional and home spa use.

Peach Extract FormulaExfoliating & MoisturizingSuitable for Daily Foot Care
Peach exfoliating foot scrub mask
This peach exfoliating foot scrub mask combines natural peach extract, fruit acids, and salicylic acid to gently soften and dissolve dead skin cells. The dual action of exfoliation and acids deeply cleanses rough, dead skin on the feet while replenishing moisture and nutrients, leaving feet noticeably softer, smoother, and more supple.
Target Markets Beauty care brands, spa suppliers, online skincare merchants, and foot care retailers seeking private label exfoliating foot products.
MOQ 1000 units
Lead Time 30-40 days after sample approval and packaging confirmation
Compliance Product can support cosmetic regulatory filing as required; third-party testing available upon request.
Customization Formula, fragrance, packaging, and branding design can be customized according to brand needs.

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
Normal skinDry skinRough skinCracked heels

1、Applicability

professional spa treatments, home spa use, tired feet care, rough skin renewal

2、Main Functions

gentle peach exfoliation, dead skin removal, deep cleanse and hydrate, soften and smooth feet

3、Suitable Population

Adults who suffer from dry or rough feet; salon professionals; personal foot care users.

Formula Customization Options

What you can change (and how far).
F
Formula & IngredientsCustomize exfoliating intensity, scent, and active botanical extracts.
P
Packaging FormAvailable in sachets, tubes, or jar sets per brand positioning.
L
Label & BrandingCustom graphics and logo printing according to brand CI.
T
Texture & FragranceControl the creaminess and aroma intensity — peach, citrus, or fragrance-free.
S
Sample DevelopmentFree initial formula testing and sample preparation before mass production.
R
Regulatory AssistanceSupport for ingredient documentation and local compliance filing.

Packaging & Craftsmanship

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

Packaging Options

Individual sachetPlastic jar with screw capPE tubeFoot-shaped pouchSet box packaging

Decoration & Finishing

Matte finish printingGloss labelHot foil stampingTransparent window designEmbossed logo
Recommended Packaging
Convenient single-use sachets are popular for trial and retail sets; customized designs available upon request.
Ask for Packaging Options

MOQ & Lead Time

MOQ
Flexible small-batch starting at 1000 pieces for new brand promotions.
Sampling
Sample preparation generally within 3–5 working days after formula confirmation. (1–3 formula options)
Bulk Production
Bulk production typically completed within 30–40 days following packaging readiness. after final approval
OEM Scope
Full-process OEM/ODM including product formulation, packaging design, and compliance documentation with support for beauty, retail, and spa brands.
Incoterms: EXW/FOB Guangzhou available upon request. Shelf-life: Estimated 24 months under standard storage conditions; confirm via stability test if needed.

Testing & Documents (Available)

Microbiological Test

Conducted to ensure product safety and preservation stability.

Dermatological Compatibility

Test available upon request to evaluate mildness on skin.

Stability Test

Monitors ingredient integrity and texture under various temperatures.

Buyer-ready checklist
Request the document set you need for your region.
Email our team
What QA checkpoints should buyers audit for body care filling, batching, and fragrance dosing?

QA checkpoints are critical for body care manufacturing in SEA, focusing on batching, filling, and fragrance dosing to prevent defects and ensure market readiness. Audit batching for raw material COA verification, batch formula adherence, and viscosity/pH measurements; filling for fill volume accuracy via checkweighers, leakage tests under pressure, and capping torque; fragrance dosing for precision scales, compatibility tests to avoid separation, and sensory evaluation. Concrete details: MOQ typically starts at 3000 units, influenced by packaging; sampling timeline is 4-6 weeks; testing includes microbial, stability, and packaging drop tests; lead time from PO is 10-12 weeks, with packaging compliance for SEA regulations. We support documentation like test reports and certificates, but final regulatory approval is the buyer's responsibility, as requirements vary by country.

What is the best shipping method for body care to Southeast Asia to reduce leakage and heat damage?

For the SEA market, sea freight in a refrigerated (reefer) or at minimum a ventilated container is the standard choice. This method avoids the drastic air pressure changes of air freight, which is the primary cause of pump and spray valve failure and leakage. The stable, cooler environment also protects heat-sensitive ingredients like butters, vitamins, and certain emulsifiers from separating or degrading during the 3-5 week voyage. We coordinate the container booking, inland trucking, and export customs clearance as part of a full FOB service. Key steps include a 48-hour inverted leakage test on all sealed units post-filling and using desiccants in master cartons to manage humidity. For urgent, small batches, air freight is possible but requires specific packaging validation: we must test the final packed product in a vacuum chamber to simulate cabin pressure and use thicker, inner bubble wrap to cushion pumps. We can provide the packing list, commercial invoice, and Certificate of Origin needed for your import agent. Always factor in at least 7-10 days for customs clearance at destinations like Indonesia or Vietnam.

What are the pros and cons of aluminum-free deodorant for Southeast Asia buyers?

Aluminum-free deodorants are popular in Southeast Asia due to growing demand for natural and halal-compliant personal care, aligning with clean beauty trends. This offers a marketing edge for brands targeting health-conscious buyers. However, these formulas can have reduced antiperspirant efficacy, which is a con in humid SEA climates, requiring careful formulation with alternatives like zinc ricinoleate for odor control. MOQ guidance typically starts at 5,000 units to cover setup costs, with sampling taking 3-4 weeks for development and feedback. We assist with testing and documentation, including safety assessments and halal certification support, though final regulatory approval depends on local authorities. Packaging must be humidity-resistant, using materials like PET or secure closures to prevent leakage. Lead time from order to shipment is around 10-12 weeks, including production, QA checks, and doc preparation. By collaborating on formulation and compliance, we ensure a smooth launch for your brand.

How do you formulate a deodorant for Southeast Asia humidity to control odor and sweat feel?

Formulating deodorants for Southeast Asia's humid climate focuses on sweat control and odor prevention. Key ingredients include aluminum salts to reduce perspiration, and antimicrobials like triclosan alternatives to combat bacteria. We adjust viscosity for easy application in heat, ensuring no sticky residue, and use fragrance blends that mask odor without irritation. For MOQ, typical orders start at 5,000 units per SKU, scalable based on packaging complexity. Sampling takes 2-3 weeks for lab samples and 4 weeks for finished prototypes, including stability checks at high humidity. Testing covers microbial limits, pH balance, and 3-month accelerated stability under tropical conditions. We assist with documentation for ASEAN compliance, such as CPNP filings and IFRA certificates, but do not guarantee approval—we provide test reports and safety assessments. Packaging uses moisture-barrier materials like aluminum roll-ons or airless pumps to prevent leakage. Lead time from production to shipping is 6-8 weeks, with QA checkpoints for fill accuracy and label adhesion in humid environments. We recommend pilot runs to validate performance before full-scale production.

How do buyers compare body care suppliers for Southeast Asia: compliance, QA, pricing, and consistency?

When comparing body care suppliers for Southeast Asia, prioritize compliance with the ASEAN Cosmetic Directive (ACD). Key documents include Product Information Files (PIFs), safety assessments, and ingredient declarations. Suppliers must handle local notifications in countries like Thailand or Indonesia, and we assist with documentation, though approval relies on authorities. For QA, demand in-house testing for microbial limits, heavy metals, and preservative efficacy under high humidity to prevent spoilage. Stability testing should cover 3-6 months at elevated temperatures to ensure shelf life. Packaging must be vetted for leakage resistance and label adhesion in humid conditions to avoid rework. Pricing transparency hinges on MOQ drivers: typical MOQs are 3,000-10,000 units per SKU, influenced by custom packaging, raw material grades, and formula complexity. Consistency requires ISO-certified production with batch records, viscosity checks, and third-party audits for color and fragrance uniformity. Sampling takes 2-4 weeks, while production lead time is 45-60 days, including raw material sourcing and pilot runs. We support with testing and docs, but final compliance is buyer's responsibility.

What are common reasons body care products fail stability tests in tropical markets?

Body care products in tropical SEA markets commonly fail stability tests because high humidity and temperatures accelerate microbial contamination, leading to spoilage and safety issues. Formulations may separate, change viscosity, or lose efficacy under these conditions. Packaging materials like labels can bubble, and seals may degrade, increasing leakage risks during storage or transit. From our OEM experience, controlling fill temperature windows and conducting microbial hold-time studies are critical to prevent failures during production. For MOQ guidance, we advise a minimum of 5000 units per SKU to allow adequate batch sizes for stability testing, ensuring cost-effective scaling without compromising quality. Sampling typically takes 4-6 weeks, including accelerated stability cycles that simulate tropical climates to identify issues early. We support documentation such as stability reports and microbial testing to help meet regulatory standards, though approval depends on local authorities. Use moisture-resistant packaging like sealed pumps and UV-protected bottles to enhance durability. Lead time may extend by 2-3 weeks for additional testing phases, so plan launches accordingly to avoid delays. Always consider rework risks if initial tests fail, and factor in extra time for adjustments based on real-time environmental simulations in our facility.

How do you choose pump and foamer components that resist clogging in humid climates?

For SEA's humid climate, component selection is critical. We specify pumps with internal mechanisms made from polypropylene (PP) or acetal, which resist moisture absorption and swelling. Spring materials are stainless steel to prevent rust, which is a common failure point that leads to clogging or inconsistent dispensing. The sealing gasket material is also chosen for its resistance to mold and degradation in constant 80%+ RH environments. During sampling, we run salt spray tests on metal components and function-tests units after exposure to high humidity chambers. For production, we implement inline checks on every batch, including a torque test to ensure the actuator hasn't become stiff or stuck due to material expansion. We can support documentation like MSDS for all components and a Declaration of Conformity for the assembled packaging. Lead time for tooling new components is 45-60 days, with a standard MOQ of 10,000 units per component. Final packaging includes silica gel in master cartons to control moisture during ocean freight.

What hidden costs surprise U.S. private label buyers (testing scope, packaging rework, freight damage)?

The biggest “hidden” cost is testing scope creep. What starts as basic checks can expand into micro/stability/challenge and claim-support testing depending on positioning and channels. We can help arrange send-out testing and track reports, and we can support the documentation set you’ll need for your supply chain, but we never promise regulatory outcomes. Packaging rework is #2. After the first sample, brands commonly revise artwork, instructions, pricing sheets, or component specs (pump/cap fit, label size, box dielines). Packaging lead times add up: outer cartons are often ~15 working days for a single box, ~20 for a set box; inner packs can be ~15 for glass bottles, ~30 for acrylic, ~15 for tubes/mask pouches. Changing components midstream usually triggers re-order minimums and new proofs. Freight damage is #3. Fragile packs (glass, pumps) can require extra inserts, stronger master cartons, and better palletization. Without planning, you may pay for replacements, rework labor, and expedited shipping. Typical MOQs are 1,000-3,000 units (simple items like masks can start at 1,000; complex skincare sets often 3,000). Production is commonly 10-20 working days once everything is confirmed, while full one-stop brand delivery is often 45-60 days.

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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 brand credentialsProvide business license and trademark information for processing eligibility.
2
Define product requirementsDiscuss formula preferences, fragrance, and packaging.
3
R&D formulationOur engineers prepare the initial lab formulation per request.
4
Sample sending and confirmationReceive physical samples for evaluation and feedback.
5
Contract & depositConfirm formula and sign production contract.
6
Packaging design & orderProfessional design assistance and packaging procurement.
7
Production & quality checkBulk production, inspection, and delivery.
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