FDA.reportPublic FDA data

Inofoam Antibacterial Foaming Hand Wash

Manufacturer
Avro Enterprises, LLC | Fuller Industries, Inc
Effective date
2023-11-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:02:27

Label at a glance#

ProductInofoam Antibacterial Foaming Hand Wash
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Indications and uses

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

Dosage and administration

• 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.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warings

WARNINGS SECTION

For external use only.

When using this product 

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation and redness develop or if condition persists for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

• 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

INACTIVE INGREDIENT SECTION

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:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label02Label02

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN1
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD1
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY1
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73062-033-01Inofoam Antibacterial Foaming Hand Wash1000 mL in 1 BAGLIQUID10001
73062-033-01Inofoam Antibacterial Foaming Hand Wash1 in 1 CARTONLIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73062-033INOFOAM ANTIBACTERIAL FOAMING HAND WASH (BENZALKONIUM CHLORIDE) LIQUID [AVRO ENTERPRISES, LLC]1Current NDC, 2 package rows20231120_6615a17f-4e0a-405d-b60c-da50267d17db.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73062-03373062-033-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM LAURETH-3 SULFATEBPV390UAP0IACT
COCO MONOISOPROPANOLAMIDE21X4Y0VTB1IACT
SODIUM SULFATE0YPR65R21JIACT
MAGNESIUM NITRATE77CBG3UN78IACT
MAGNESIUM CHLORIDE02F3473H9OIACT
ALCOHOL3K9958V90MIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
FD&C RED NO. 4X3W0AM1JLXIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Inofoam Antibacterial Foaming Hand WashBENZALKONIUM CHLORIDEAvro Enterprises, LLC6615a17f-4e0a-405d-b60c-da50267d17db2023-11-17WarningsExact identifier
ndc (package): 73062-033-01
ndc (product): 73062-033
ndc11 (package): 73062003301
spl id: 0a5ec655-d06c-cb78-e063-6294a90aee74
spl set id: 6615a17f-4e0a-405d-b60c-da50267d17db

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.