FDA.reportPublic FDA data

Eye Makeup Remover

Manufacturer
Longway Technology(Guangzhou) Co., Ltd | Medical Group Care LLC
Effective date
2026-03-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:49:54

Label at a glance#

ProductEye Makeup Remover
Active ingredientALLANTOIN
Label structure10 sections

Dosage and administration

Apply with a cotton pad on closed eye lids, morning or night

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Allantoin 0.05%

Purpose

OTC - PURPOSE SECTION

skin protectant

Directions

DOSAGE & ADMINISTRATION SECTION

Apply with a cotton pad on closed eye lids, morning or night

Warnings

WARNINGS SECTION

Avoid Direct Contact in Eyes. Rinse thoroughly if contact occurs. If skin irritation or rash develops, discontinue use. 

Do Not Use

OTC - DO NOT USE SECTION

If Irritation Occurs

When Using

OTC - WHEN USING SECTION

Avoid Direct Contact in Eyes

When Using

OTC - WHEN USING SECTION

Avoid Direct Contact in Eyes

Use

INDICATIONS & USAGE SECTION

Remove makeup from eye area

Ingredients

INACTIVE INGREDIENT SECTION

WATER, HEXYLENE GLYCOL, SODIUM LAURETH SULFATE, PHENOXYETHANOL, DISODIUM PHOSPHATE, IMIDAZOLIDINYL UREA, DISODIUM EDTA, ALLANTOIN, o-CYMEN-5-OL, POTASSIUM PHOSPHATE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130050428269350GTIN-13: 0050428269350
EAN-13: 0050428269350
GTIN-12: 050428269350
UPC-A: 050428269350
GTIN storage (14 digits): 00050428269350		CVS Eye Makeup Remover.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85161-300-04Eye Makeup Remover118 mL in 1 PACKAGELIQUID1181

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85161-30085161-300-04

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
PHENOXYETHANOLHIE492ZZ3TIACT
DISODIUM PHOSPHATE22ADO53M6FIACT
IMIDAZOLIDINYL UREAM629807ATLIACT
EDETATE DISODIUM7FLD91C86KIACT
O-CYMEN-5-OLH41B6Q1I9LIACT
POTASSIUM PHOSPHATEB7862WZ632IACT
ALLANTOIN344S277G0ZACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4d787d48-d209-d6e4-e063-6294a90abc001a6191d6-6b75-4d33-81c3-7fc705b41bb52026-03-20WarningsExact identifier
spl set id: 1a6191d6-6b75-4d33-81c3-7fc705b41bb5

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.