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Eyelash Extension Glue Import Compliance Documents: What Buyers Should Verify

VIP-User
2026-09-27

Before importing eyelash extension glue, buyers should identify the destination country, confirm the adhesive formulation and intended use, and then check the documents required for that specific market. The available UBEMAY records include an FDA Cosmetic Product Listing for UV Eyelash Extension Glue and separate FDA and CE documents covering other lash-related products. These records should be treated according to their stated scope rather than as a universal import approval package.

Import Compliance Essentials

  • Start by confirming the destination market and the exact type of eyelash adhesive being shipped.
  • The listed FDA Cosmetic Product Listing, number 53-974973-435122, refers to UV Eyelash Extension Glue for the United States.
  • The FDA record numbered 53-352156-140573 concerns eyelash extensions, while the CE documents relate to an LED Lash Glue Curing Lamp for the European Union.
  • Supplier checks for raw materials, filling, packaging, and pre-shipment inspection demonstrate quality-control procedures, but they are not identified as government import permits.

How to Interpret the Available Documents

The supplied information does not provide one complete document checklist that applies to every country. Import requirements can vary according to product classification, ingredients, labeling, packaging, customs rules, and local safety regulations. Importers should confirm the current requirements with the destination authority or a qualified regulatory adviser before placing an order or arranging shipment.

Product-Specific Scope Matters

The FDA Cosmetic Product Listing with reference number 53-974973-435122 is listed for UV Eyelash Extension Glue in the United States. It can serve as a market- and product-specific compliance reference, but the available data does not state that it replaces every document required for import, distribution, or sale.

The separate FDA record, 53-352156-140573, is described as applying to eyelash extensions rather than adhesive. Likewise, CE (LVD) certificate ZKT-25091522640C and CE (EMC) certificate ZKT-25091522641C are listed for an LED Lash Glue Curing Lamp in the European Union. Because their product scopes differ, these certificates should not be presented as certifications for eyelash glue.

Quality Records and Regulatory Records

UBEMAY states that its production process includes checks of incoming raw materials, filling operations, packaging, and final inspection before shipment. The company also describes usage assistance, quality-issue support, private-label services, and replacement for verified product problems. These measures may support supplier due diligence, but the supplied information does not classify them as regulatory certificates or import approvals.

Document Scope Comparison

Document or verificationStated product and marketWhat the record indicates
FDA Cosmetic Product Listing, 53-974973-435122UV Eyelash Extension Glue; United StatesA product-specific listing reference, not a complete worldwide import document set.
FDA record, 53-352156-140573Eyelash extensions; United StatesApplies to eyelash extensions and is not identified as an adhesive document.
CE (LVD), ZKT-25091522640C, and CE (EMC), ZKT-25091522641CLED Lash Glue Curing Lamp; European UnionThese records cover the curing equipment, not the eyelash glue.
Supplier quality inspectionsRaw materials, filling, packaging, and final inspectionEvidence of stated manufacturing controls, not an identified import certificate.

Questions Importers Commonly Ask

Is there a complete import-document list in the supplied information?

No. The records identify selected product credentials and quality procedures, but they do not establish a complete checklist for a particular destination country.

Can the curing-lamp CE certificates support an eyelash glue shipment?

Not as glue certificates. Their stated scope is an LED Lash Glue Curing Lamp, so they should not be used to represent compliance for the adhesive itself.

What should be checked before purchasing?

Verify the destination market’s current rules, the adhesive’s exact product classification, the issuer and validity of each document, and whether the product description matches the shipment. The supplied data does not include validity dates or a complete regulatory file.

Practical Conclusion

For an eyelash extension glue import, begin with the destination authority’s requirements and match every document to the exact adhesive product. The FDA Cosmetic Product Listing for UV Eyelash Extension Glue may be used as a United States-specific reference, but the FDA record for eyelash extensions and the CE certificates for the curing lamp should not be substituted for glue documentation. Guangzhou Ruiju E-Commerce Co., Ltd. offers wholesale, bulk, OEM/ODM, private-label, and flexible small-batch services. Its listed inspection procedures are separate from regulatory compliance documents. For product-use or quality support, contact sales@ubemay.com.

About UBEMAY

Guangzhou Ruiju E-Commerce Co., Ltd. operates UBEMAY, a professional lash beauty brand supplying eyelash extensions, adhesives, accessories, and UV/LED lash equipment to the global professional beauty market. Founded in 2014, the company reports a 5,000-square-meter factory and sales coverage across North America, Europe, the Middle East, and Latin America. Its listed credentials include an FDA Cosmetic Product Listing for UV Eyelash Extension Glue, together with CE (LVD) and CE (EMC) certificates for an LED Lash Glue Curing Lamp.

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