FDA.reportPublic FDA data

Gentle Eye Makeup Remover

Manufacturer
Longway Technology(Guangzhou) Co., Ltd | Medical Group Care LLC
Effective date
2026-03-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:50:59

Label at a glance#

ProductGentle Eye Makeup Remover
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Dosage and administration

Shake well. Apply with a cotton pad on closed eye lids. Gently Rinse with warm water.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

antiseptic

Directions

DOSAGE & ADMINISTRATION SECTION

Shake well. Apply with a cotton pad on closed eye lids. Gently Rinse with warm water.

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 skin irritation or rash develops

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, Cyclopentasiloxane, Sodium Chloride, Poloxamer 184, Benzalkonium Chloride, Disodium Phosphate, Aloe Barbadensis Leaf Water, Cucumis Sativus (Cucumber) Extract, Butylene Glycol, Potassium Phosphate, Glycerin, Allantoin, Dipropylene Glycol, Hydroxyacetophenone, Cyclohexasiloxane

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130050428269428GTIN-13: 0050428269428
EAN-13: 0050428269428
GTIN-12: 050428269428
UPC-A: 050428269428
GTIN storage (14 digits): 00050428269428		CVS Gentle Eye Makeup Remover.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85161-301-08Gentle Eye Makeup Remover244 mL in 1 PACKAGELIQUID2442

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85161-30185161-301-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CYCLOPENTASILOXANE0THT5PCI0RIACT
SODIUM CHLORIDE451W47IQ8XIACT
POLOXAMER 184BIS92ZSF57IACT
DISODIUM PHOSPHATE22ADO53M6FIACT
ALOE BARBADENSIS LEAF JUICERUE8E6T4NBIACT
CUCUMIS SATIVUS (CUCUMBER) JUICE61845009SPIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
POTASSIUM PHOSPHATEB7862WZ632IACT
GLYCERINPDC6A3C0OXIACT
ALLANTOIN344S277G0ZIACT
DIPROPYLENE GLYCOLE107L85C40IACT
HYDROXYACETOPHENONEG1L3HT4CMHIACT
CYCLOHEXASILOXANEXHK3U310BAIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
53fc113b-1b6f-de65-e063-6394a90a7fc4db87d81c-bd6c-47dd-8d4c-61b6b1155ce82026-06-11WarningsExact identifier
spl set id: db87d81c-bd6c-47dd-8d4c-61b6b1155ce8

Reported adverse events (FAERS/openFDA)#

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