ANTIBACTERIAL- benzalkonium chloride solution

Antibacterial by

Drug Labeling and Warnings

Antibacterial by is a Otc medication manufactured, distributed, or labeled by Sam's West, Inc., Korex Chicago LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride (0.13%)

Purpose

Antiseptic Handwash

Use

• For handwashing to decrease bacteria on skin

Warnings

For external use only

Do not use In eyes

When using this product

• If in eyes, rinse promptly and thoroughly with water
• Discontinue use if irritation and redness develop

Stop use and ask a doctor if

• Skin irritation or redness occurs for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Wet hands Apply 5mL (teaspoonful) or palmful to hands and forearms Rub vigorously for 20 seconds Wash between fingers, around fingernails and backs of hands Rinse thoroughly with warm water Dry with paper towels or air-dry

Other information

For additional information, see Safety Data Sheet (SDS) For emergency medical information, call 1-866-767-5045

Inactive ingredients

Water, Cetrimonium chloride, Lauramine oxide, Cocamide MIPA, Lauramidopropylamine oxide, Sodium benzoate, PEG-120 methyl glucose dioleate, Citric acid, Glycerin, Sodium chloride, Fragrance, Disodium EDTA, Red 40.

PRINCIPAL DISPLAY PANEL

NDC: 68196-665-01

1

GALLON

M

Member's

Mark™

ANTIBACTERIAL

HAND SOAP

COMMERCIAL GRADE

KILLS 99.9% OF GERMS*

FRESH CLEAN FRAGRANCE

NET CONTENTS 1 GALLON (3.78 L)

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68196-665
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 g  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM BENZOATE (UNII: OJ245FE5EU)
WATER (UNII: 059QF0KO0R)
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
EDETATE DISODIUM (UNII: 7FLD91C86K)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
COCAMIDE MIPA (UNII: 21X4Y0VTB1)
RED 40 (UNII: WZB9127XOA)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)

Product Characteristics
Color	red	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68196-665-01	3.785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/2025
2	NDC: 68196-665-04	4 in 1 CARTON	01/01/2025
2		3.78 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/01/2025

Labeler - Sam's West, Inc. (051957769)

Registrant - Korex Chicago LLC (792133147)