We are a professional OEM cosmetics manufacturer manufacturer |

We support emerging beauty brands, established brands, distributors, retailers, salons and spas that need private label, OEM, ODM or contract manufacturing support.

Yes. Depending on scope, INTE can support concept review, formulation or sample-based customization, packaging coordination, filling, labeling, packing, quality documentation and delivery planning.

Yes. These are core product areas for our B2B manufacturing projects. We can also review related personal-care formats, including masks, ampoules, body care, fragrance and selected makeup formats.

Yes. A ready formula or an adjusted formula can be the fastest route. We will confirm whether the formula, ingredients, packaging and claims are suitable for your target market.

We can review trend-led ingredient concepts and assess formulation feasibility, stability, compatibility, dosage, claims and target-market requirements. The final formula depends on the product format, ingredient version, packaging and compliance review.

Yes, these concepts can be evaluated through ingredient selection, texture, fragrance, preservative system, packaging compatibility and target-market claims. We recommend defining the intended consumer and claim language before sample development.

Sample-based customization is available subject to technical feasibility, ingredient availability, intellectual-property considerations and the requested performance target. A benchmark sample is a starting reference, not a guarantee of an identical formula.

Yes. Please include preferred ingredients, exclusions, target texture, scent, color, finish, skin or hair concern and target market in the development brief.

We can screen ingredients and develop toward a requested positioning. Official certification, market-specific definitions and registration responsibilities must be reviewed separately and confirmed for the final formula.

Sunscreen projects require early confirmation of the target country, UV filters, SPF or protection claims, testing plan, packaging and regulatory route. We can review the project scope before confirming feasibility and timing.

As a planning guide, standard bottles and droppers often start at 5,000 units; single-use formats may start at 5,000 boxes; special bottle formats and fragrance may start at 10,000 units; glass ampoule components may require 100,000 sticks. Exact MOQ is confirmed by SKU and packaging route.

Usually, each SKU and packaging route requires its own workable production quantity. We can review a multi-SKU launch plan and recommend a practical combination of formulas, packaging and volumes.

It starts after the product function, ingredient direction and development requirements are confirmed. It does not automatically include courier transit, custom packaging sampling or additional testing.

It starts after formula, artwork, packaging, quantity and production details are approved, required materials are available and the project is released for production. The confirmed project schedule is the controlling timeline.

A faster route may be possible when an existing formula and standard packaging are available. Custom formulas, special components, additional testing and international logistics can extend the schedule. Rush feasibility must be confirmed case by case.

Customer-supplied packaging can be reviewed for specification, compatibility, usable quantity and production responsibility before approval. Please share drawings, material information, dimensions and delivery timing with the project brief.

We can review packaging requirements and coordinate suitable stock or custom options. Custom molds, decoration, printing and packaging minimums may affect cost and lead time.

Packaging solutions can include labels, cartons and other secondary packaging. The artwork, engineering and design scope should be confirmed for each project before production.

We can coordinate the project from product concept and formulation through packaging, filling, packing, documentation and delivery planning, with the exact scope defined in the quotation.

The supplied certificate package includes ISO 22716:2007 and US FDA CFSAN Cosmetic GMP certificates for Yingte Cosmetics (Guangdong) Co., Ltd. The certificates shown are valid from 23 July 2025 to 22 July 2028, subject to surveillance and the stated scope. The contracting entity and certified manufacturing entity should be confirmed for each project.

No. ISO 22716 and GMP describe manufacturing-practice controls and do not by themselves approve every finished product, prove efficacy or replace destination-market requirements.

Depending on the SKU and target market, available documents may include INCI information, MSDS/SDS, formulation information, batch or test records, stability or compatibility studies and efficacy reports. The final document list should be agreed before production.

Selected products have third-party testing and 28-day human efficacy reports. Not every formula has human efficacy testing. If a specific claim requires additional evidence, we can review the testing plan and responsible party.

We can review the product, formula, claims, label, documents and target market at project start. The responsible party for safety assessment, product information, notification, registration or market filings must be agreed separately for the final destination.

A cleanroom classification report is different from an ISO 22716 or GMP certificate. If a buyer requires a specific cleanroom grade, test date, testing body or area scope, this should be confirmed with the factory before publication or quotation.

We support global B2B projects, subject to the product, destination, order volume, shipping route, customs requirements and market documentation. Please include the destination country in your first inquiry.

Please share the product type, target market, formula direction or benchmark, active ingredients, claims, fill size, packaging preference, quantity, artwork status and delivery destination.

Yes. Samples can be developed or selected for project evaluation before bulk approval. Sample scope, timing, fees and courier arrangements should be confirmed for the specific product.

Submit a product brief through the inquiry form or contact our team directly. We will review the project, identify missing information, recommend a development route and confirm the next step.