XTRA SQUEEZE ANTIBACTERIAL HAND FRESH LEMON- benzalkonium chloride gel

XTRA Squeeze Antibacterial Hand Fresh Lemon by

Drug Labeling and Warnings

XTRA Squeeze Antibacterial Hand Fresh Lemon by is a Otc medication manufactured, distributed, or labeled by MY IMPORTS USA LLC., Zhejiang Jifu Daily Chemical Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

For handwashing, to reduce bacteria on skin

Warnings

For external use only.

Keep out of reach of children

Keep out of reach od children

Avoid contact with eyes. If eye contact occures flush thoroughly with water.

Do not use with chlorine bleach to avoid irritating fumes.

Do not ingest. If ingested, drink plenty of water, contact a physician.

STORAGE AND HANDLING

Store in a cool and dry place, and avoid direct sunlight.

Directions

Squeeze liquid onto hands, scrub and rinse by water thoroughly.

Inactive ingredients

Water (Aqua)

Sodium Laureth Sulfate

Sodium Chloride

Decyl Glucoside

Sodium Benzoate

Phenoxyethanol

Fragrance

Citric Acid

Methylisothiazlinone

Label

INGREDIENTS AND APPEARANCE

XTRA SQUEEZE ANTIBACTERIAL HAND FRESH LEMON 
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51628-4502
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PHENOXYETHANOL (UNII: HIE492ZZ3T)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
SODIUM BENZOATE (UNII: OJ245FE5EU)
AQUA (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
CITRIC ACID (UNII: 2968PHW8QP)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Product Characteristics
Color		Score
Shape		Size
Flavor	LEMON	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51628-4502-1	458 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/09/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	07/09/2025

Labeler - MY IMPORTS USA LLC. (195767988)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Jifu Daily Chemical Co., Ltd.		710111693	manufacture(51628-4502)