INOFOAM ANTIBACTERIAL FOAMING HAND WASH- benzalkonium chloride liquid

Inofoam Antibacterial Foaming Hand Wash by

Drug Labeling and Warnings

Inofoam Antibacterial Foaming Hand Wash by is a Otc medication manufactured, distributed, or labeled by Avro Enterprises, LLC, Fuller Industries, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Uses

• Handwash to help reduce bacteria on the skin that potentially can cause disease. 
• Recommended for repeated use.

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:

INGREDIENTS AND APPEARANCE

INOFOAM ANTIBACTERIAL FOAMING HAND WASH 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73062-033
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 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73062-033-01	1 in 1 CARTON	11/20/2023
1		1000 mL in 1 BAG; 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)	11/20/2023

Labeler - Avro Enterprises, LLC (804030166)

Establishment
Name	Address	ID/FEI	Business Operations
Fuller Industries, Inc		078704329	manufacture(73062-033)