FDA.reportPublic FDA data

Problend E3 Foaming Hand Sanitizer

Manufacturer
Seatex, LLC
Effective date
2022-09-19
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-05-31 23:50:48

Label at a glance#

ProductProblend E3 Foaming Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure15 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose

Benzalkonium Chloride 0.1%...................Antimicrobial

INDICATIONS & USAGE SECTION

Uses

For hand sanitizing to decrease bacteria on the skin.

Recommended for repeated use.

OTC - WHEN USING SECTION

When using this product Avoid contact with eyes. In case of eye contact, flush eyes with water. Do not ingest.

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.

DOSAGE & ADMINISTRATION SECTION

Directions

Pump a small amount of foam into palm of hand.

Rub thoroughly over all surffaces of both hands

Rub hands together briskly until dry.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Water, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops and conditions persist.

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

WARNINGS SECTION

Warnings For External use only.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1 gl label1 gl label3.785 L 76250-120-01

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

330 gl label330 gl label1249 L 76250-120-30

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

55 gl label55 gl label208 L 76250-120-55

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

275 gl label275 gl label1041 L 76250-120-75

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1.25 L Front Label1.25 L Front Label1.25 L Front 76250-120-25

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1.25 L Back Label1.25 L Back Label1.25 L Back 76250-120-25

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN6
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD6
1038799benzalkonium chloride 0.1 % Topical FoamSY6

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76250-120-012024-01-30C16284748780-11030e365-0eb2-111a-e063-dadaa90a10e227120 Sanitizer Foam Bulk
76250-120-252024-01-30C16284748780-11030e365-0eb2-111a-e063-dadaa90a10e227120 Sanitizer Foam Bulk
76250-120-302024-01-30C16284748780-11030e365-0eb2-111a-e063-dadaa90a10e227120 Sanitizer Foam Bulk
76250-120-552024-01-30C16284748780-11030e365-0eb2-111a-e063-dadaa90a10e227120 Sanitizer Foam Bulk
76250-120-752024-01-30C16284748780-11030e365-0eb2-111a-e063-dadaa90a10e227120 Sanitizer Foam Bulk

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76250-120-01Problend E3 Foaming Hand Sanitizer3785 g in 1 BOTTLESOAP37856
76250-120-25Problend E3 Foaming Hand Sanitizer1250 g in 1 CARTRIDGESOAP12506
76250-120-30Problend E3 Foaming Hand Sanitizer1249000 g in 1 TANKSOAP12490006
76250-120-55Problend E3 Foaming Hand Sanitizer208000 g in 1 DRUMSOAP2080006
76250-120-75Problend E3 Foaming Hand Sanitizer1041000 g in 1 TANKSOAP10410006

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76250-120PROBLEND E3 FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) SOAP [SEATEX, LLC]6Legacy NDC, 5 package rows20220920_b3ecada5-37ea-13f7-e053-2995a90aac50.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76250-12076250-120-01, 76250-120-30, 76250-120-55, 76250-120-75, 76250-120-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
LAURTRIMONIUM CHLORIDEA81MSI0FICIACT
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
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
e90f5405-989c-d413-e053-2a95a90ab943b3ecada5-37ea-13f7-e053-2995a90aac502022-09-19WarningsExact identifier
spl id: e90f5405-989c-d413-e053-2a95a90ab943
spl set id: b3ecada5-37ea-13f7-e053-2995a90aac50

Reported adverse events (FAERS/openFDA)#

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