GENTLE EYE MAKEUP REMOVER- benzalkonium chloride liquid

Gentle Eye Makeup Remover by

Drug Labeling and Warnings

Gentle Eye Makeup Remover by is a Otc medication manufactured, distributed, or labeled by Longway Technology(Guangzhou) Co., Ltd, Medical Group Care LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

antiseptic

Directions

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

Warnings

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

Do Not Use

If skin irritation or rash develops

When Using

Avoid Direct Contact in Eyes

Keep out of reach of children

Use

Remove makeup from eye area

Ingredients

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GENTLE EYE MAKEUP REMOVER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85161-301
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CYCLOPENTASILOXANE (UNII: 0THT5PCI0R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
POLOXAMER 184 (UNII: BIS92ZSF57)
DISODIUM PHOSPHATE (UNII: 22ADO53M6F)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
CUCUMIS SATIVUS (CUCUMBER) JUICE (UNII: 61845009SP)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
POTASSIUM PHOSPHATE (UNII: B7862WZ632)
GLYCERIN (UNII: PDC6A3C0OX)
ALLANTOIN (UNII: 344S277G0Z)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
CYCLOHEXASILOXANE (UNII: XHK3U310BA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85161-301-08	244 mL in 1 PACKAGE; Type 0: Not a Combination Product	03/13/2028

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	03/13/2026

Labeler - Longway Technology(Guangzhou) Co., Ltd (844528915)

Registrant - Medical Group Care LLC (085137089)