FDA.reportPublic FDA data

Inofoam Antibacterial Foaming Hand Wash

Product NDC
73062-033
11-digit product format
730620033
Labeler code
73062
Product ID
73062-033_0a5ec655-d06c-cb78-e063-6294a90aee74
Type
HUMAN OTC DRUG
Nonproprietary name
BENZALKONIUM CHLORIDE
Dosage form
LIQUID
Route
TOPICAL
Labeler
Avro Enterprises, LLC
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-11-20
Substance
BENZALKONIUM CHLORIDE
Active strength
1.3 mg/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Inofoam Antibacterial Foaming Hand Wash
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZALKONIUM CHLORIDE1.3 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
F5UM2KM3W7Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1046593Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
6615a17f-4e0a-405d-b60c-da50267d17dbAvailable on FDA.report

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

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 (product): 73062-033

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN6615a17f-4e0a-405d-b60c-da50267d17db1
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD6615a17f-4e0a-405d-b60c-da50267d17db1
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY6615a17f-4e0a-405d-b60c-da50267d17db1
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY6615a17f-4e0a-405d-b60c-da50267d17db1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
73062-033-01730620033011 BAG in 1 CARTON (73062-033-01) / 1000 mL in 1 BAG1 bag2023-11-20NoNoCurrent