INOFOAM ANTIBACTERIAL FOAMING HAND WASH- benzalkonium chloride liquid 
Avro Enterprises, LLC

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Inofoam Antibacterial Foaming Hand Wash

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13%

Purppose

Antiseptic

Uses

Warings

For external use only.

When using this product 

Keep out of eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if

irritation and redness develop or if condition persists 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 with water and dispense sufficient amount of product into cupped palm of hand. • Wash both hands thoroughly for 15 seconds. •  Rinse under running water and dry thoroughly.

Inactive ingredients

Water, Sodium Lauryl Ether Sulfate, Cocamide MIPA, Sodium Sulfate, Fragrance, Magnesium Nitrate, Magnesium Chloride, Alcohol Denatured, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Red#4, FD&C Yellow #5

Package Labeling:

Label0

INOFOAM ANTIBACTERIAL FOAMING HAND WASH 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73062-032
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)  
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)  
SODIUM SULFATE (UNII: 0YPR65R21J)  
MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
ALCOHOL (UNII: 3K9958V90M)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73062-032-011 in 1 CARTON11/20/2023
13800 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)11/20/2023
Labeler - Avro Enterprises, LLC (804030166)
Establishment
NameAddressID/FEIBusiness Operations
Fuller Industries, Inc078704329manufacture(73062-032)

Revised: 11/2023
Document Id: 0a59627b-cad3-b9b2-e063-6394a90a2f7f
Set id: 4fc1e57f-b909-4dde-8c1a-2793af6eafb0
Version: 1
Effective Time: 20231117
 
Avro Enterprises, LLC