FOAMING HAND- benzalkonium chloride lotion 
Consumer Product Partners, LLC

----------

Antibacterial Foaming Hand Soap
224.000/224AA

Active ingredient

Benzalkonium chloride 0.13%

Purpose

Antibacterial

Use

for handwashing to decrease bacteria on the skin

Warnings

For external use only: hands only

When using this product

avoid contact with eyes. If contact occurs, rinse eyes with water.

Stop use and ask a doctor if

Keep out of reach of children.

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

Directions

Inactive ingredients

water, cocamidopropyl betaine, lauramidopropylamine oxide, lauramine oxide, myristamidopropylamine oxide, glycerin, citric acid, tetrasodium EDTA, sodium benzoate

Adverse event

Manufactured By: Vi-Jon, Inc.

St. Louis, Mo 63114

Adverse event

germ-X

Professional

ANTIBACTERIAL

FOAMING

HAND SOAP

1000 ML (33.8 FL OZ)

image description

FOAMING HAND 
benzalkonium chloride lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11344-224
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)  
GLYCERIN (UNII: PDC6A3C0OX)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
EDETATE SODIUM (UNII: MP1J8420LU)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11344-224-083785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/08/2018
2NDC:11344-224-96222 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product02/08/201804/11/2024
3NDC:11344-224-44532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/08/201802/24/2021
4NDC:11344-224-04750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/08/201804/11/2024
5NDC:11344-224-451150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/08/2018
6NDC:11344-224-2044 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product02/08/201804/11/2024
7NDC:11344-224-861000 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product02/08/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)02/08/2018
Labeler - Consumer Product Partners, LLC (119091520)
Registrant - Consumer Product Partners, LLC (119091520)
Establishment
NameAddressID/FEIBusiness Operations
Consumer Product Partners, LLC119091520manufacture(11344-224)
Establishment
NameAddressID/FEIBusiness Operations
Consumer Product Partners, LLC119091514manufacture(11344-224)

Revised: 4/2024
Document Id: 15d480dd-25a2-ef8c-e063-6294a90a43fb
Set id: 2002c182-b4a6-4baa-8497-74570713b8bb
Version: 16
Effective Time: 20240411
 
Consumer Product Partners, LLC