FDA.reportPublic FDA data

Advanced Antibacterial Foaming Hand Soap

Manufacturer
Ecolab Inc.
Effective date
2025-12-31
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:30:46

Label at a glance#

ProductAdvanced Antibacterial Foaming Hand Soap
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

for handwashing to decrease bacteria on the skin

Dosage and administration

wet hands and apply foam scrub hands and forearms rinse thoroughly and dry

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.5%

Purpose

OTC - PURPOSE SECTION

Antiseptic handwash

Uses

INDICATIONS & USAGE SECTION

  • for handwashing to decrease bacteria on the skin

Warning

WARNINGS SECTION

  • For external use only

Do not use

OTC - DO NOT USE SECTION

  • in eyes

When using the product

OTC - WHEN USING SECTION

  • if in eyes, rinse promptly and thoroughly with water
  • discontinue use if irritation and redness develop

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if skin irritation or redness occurs for more than 72 hours

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands and apply foam
  • scrub hands and forearms
  • rinse thoroughly and dry

Other information

REFERENCES SECTION

  • for additional information, see Safety Data Sheet (SDS)
  • EMERGENCY HEALTH INFORMATION: 1 800 328 0026. If located outside the United States and Canada, call collect 1 651 222 5352 (number is in the US

INACTIVE INGREDIENT SECTION

Inactive ingredients water (aqua), cocamine oxide, hexylene glycol, PEG-180, glycerin, cocamidopropyl PG-dimonium chloride phosphate, phenoxyethanol, polyquaternium 7, myristamide DIPA, myristamine oxide, citric acid, methyl gluceth-20, glyceryl caprylate/caprate, alcohol, PEG-12 dimethicone, potassium citrate, fragrance, blue 1

OTC - QUESTIONS SECTION

Questions? call 1-800-35-CLEAN (352-5326)

Representative Label and Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ecolab®

Advanced Antibacterial 

Foaming Hand Soap

Active ingredient: Benzalkonium chloride 0.5%

1200 mL (40.6 US FL OZ) 6102754

Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA ·

tel: 1 800 35 CLEAN (352 5326)

© 2024 Ecolab USA Inc. · All rights reserved

Made in U.S.A.

www.ecolab.com

Representative labelRepresentative label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1731737benzalkonium chloride 0.5 % Medicated Liquid SoapPSN9
1731737benzalkonium chloride 5 MG/ML Medicated Liquid SoapSCD9
1731737benzalkonium chloride 0.5 % Medicated Liquid SoapSY9

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130025469096647GTIN-13: 0025469096647
EAN-13: 0025469096647
GTIN-12: 025469096647
UPC-A: 025469096647
GTIN storage (14 digits): 00025469096647		label.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47593-543-41Advanced Antibacterial Foaming Hand Soap750 mL in 1 BOTTLE, PLASTICSOLUTION7509
47593-543-44Advanced Antibacterial Foaming Hand Soap1134000 mL in 1 CONTAINERSOLUTION11340009
47593-543-59Advanced Antibacterial Foaming Hand Soap1250 mL in 1 BOTTLE, PLASTICSOLUTION12509
47593-543-60Advanced Antibacterial Foaming Hand Soap1600 mL in 1 BOTTLE, PLASTICSOLUTION16009
47593-543-63Advanced Antibacterial Foaming Hand Soap1250 mL in 1 BOTTLE, PLASTICSOLUTION12509
47593-543-70Advanced Antibacterial Foaming Hand Soap1200 mL in 1 BOTTLE, PLASTICSOLUTION12009

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47593-54347593-543-60, 47593-543-63, 47593-543-59, 47593-543-41, 47593-543-44, 47593-543-70

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
COCAMINE OXIDEQWA2IZI6FIIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
POLYETHYLENE GLYCOL 8000Q662QK8M3BIACT
GLYCERINPDC6A3C0OXIACT
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATEH2KVQ74JM4IACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW)0L414VCS5YIACT
MYRISTIC DIISOPROPANOLAMIDE17DN142CTKIACT
MYRISTAMINE OXIDEJ086PM3RRTIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
METHYL GLUCETH-20J3QD0LD11PIACT
GLYCERYL MONO- AND DICAPRYLOCAPRATEU72Q2I8C85IACT
ALCOHOL3K9958V90MIACT
PEG-12 DIMETHICONEZEL54N6W95IACT
POTASSIUM CITRATEEE90ONI6FFIACT
FD&C BLUE NO. 1H3R47K3TBDIACT

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
82025-09-29monthly-update2026-06-03 17:38:11
72025-01-23full-release2026-06-01 00:53:46

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
Advanced Antibacterial Foaming Hand SoapBENZALKONIUM CHLORIDEEcolab Inc.ea6d45ee-7713-4a90-81a8-6963c7f5c2302025-12-31WarningsExact identifier
ndc (package): 47593-543-70
ndc (package): 47593-543-41
ndc (package): 47593-543-44
ndc (package): 47593-543-59
ndc (package): 47593-543-63
ndc (package): 47593-543-60
ndc (product): 47593-543
ndc11 (package): 47593054370
ndc11 (package): 47593054360
ndc11 (package): 47593054359
ndc11 (package): 47593054344
ndc11 (package): 47593054341
ndc11 (package): 47593054363
spl id: f6fa0ff7-6f71-4b1f-baa9-a6352c19c1db
spl set id: ea6d45ee-7713-4a90-81a8-6963c7f5c230

Reported adverse events (FAERS/openFDA)#

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