FDA.reportPublic FDA data

Afia Foaming E2 Sanitizing Hand Cleaner

Manufacturer
National Chemical Laboratories, Inc.
Effective date
2017-01-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:48:33

Label at a glance#

ProductAfia Foaming E2 Sanitizing Hand Cleaner
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

Uses • For hand-washing to decrease bacteria on the skin. Helps prevent cross contamination by hand contact.

Dosage and administration

• Wet hands and wrist with water. Pump 2 strokes of foam into palm of hand. • Rub thoroughly over all surfaces of both hands and wrist, include between fingers and under cuticles, for 60 seconds. • Rinse hands completely and dry thoroughly.

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient. Purpose

Benzalkonium Chloride 0.15%...........Antimicrobial hand Cleaner

ActiveActive

Uses

OTC - PURPOSE SECTION

  • Uses • For hand-washing to decrease bacteria on the skin. Helps prevent cross contamination by hand contact.

UsesUses

Warnings:

WARNINGS SECTION

Warnings For external use only.

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water. Stop use and ask a doctor if irritation or redness develops, 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.

WarningsWarnings

Directions

DOSAGE & ADMINISTRATION SECTION

• Wet hands and wrist with water. Pump 2 strokes of foam into palm of hand. • Rub thoroughly over all surfaces of both hands and wrist, include between fingers and under cuticles, for 60 seconds. • Rinse hands completely and dry thoroughly.

DosageDosage

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water / Cetrimonium Chloride / Coco Glucoside / Dihydroxyethyl Cocamine Oxide / Laurtrimonium Chloride / Glycereth-17 Cocoate / Cocamidopropyl Hydroxysultaine / Hydroxyethylcellulose / Citric Acid

Inactive ingredientsInactive ingredients

Uses

INDICATIONS & USAGE SECTION

For hand-washing to decrease bacteria on the skin. Helps prevent cross contamination by hand contact.

usesuses

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Keep out of reachKeep out of reach

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Afia Foaming E2 Sanitizing Hand Cleaner

Final PackageFinal PackageCartonCarton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapPSN2
1233282benzalkonium chloride 1 MG/ML Medicated Liquid SoapSCD2
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71023-448-572024-01-30C16284748780-11030e365-350c-111a-e063-dadaa90a10e2Listing of Afia Foaming E2 Sanitizing Hand Cleaner

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71023-448-57Afia Foaming E2 Sanitizing Hand Cleaner1000 mL in 1 BAGSOAP10002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71023-448AFIA FOAMING E2 SANITIZING HAND CLEANER (BENZALKONIUM CHLORIDE) SOAP [NATIONAL CHEMICAL LABORATORIES, INC.]2Legacy NDC, 1 package rows20170119_466478c7-ea1d-0f6c-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71023-44871023-448-57

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
HYDROXYETHYL CELLULOSE (5000 MPA.S AT 1%)X70SE62ZARIACT
GLYCERETH-17 COCOATE3057VPT0KCIACT
WATER059QF0KO0RIACT
COCO GLUCOSIDEICS790225BIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
LAURTRIMONIUM CHLORIDEA81MSI0FICIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
COCAMIDOPROPYL HYDROXYSULTAINE62V75NI93WIACT

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
466478c7-ea22-0f6c-e054-00144ff88e88466478c7-ea1d-0f6c-e054-00144ff88e882017-01-18WarningsExact identifier
spl id: 466478c7-ea22-0f6c-e054-00144ff88e88
spl set id: 466478c7-ea1d-0f6c-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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