FDA.reportPublic FDA data

Clean Force

Manufacturer
Ecolab Inc.
Effective date
2024-08-02
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:16:32

Label at a glance#

ProductClean Force
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

Warnings

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

  • READ SAFETY DATA SHEET (SDS) BEFORE USING THIS PRODUCT
  • EMERGENCY HEALTH INFORMATIN: 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 hydroxide, fragrance, blue 1

OTC - QUESTIONS SECTION

Questions? call 1.866.444.7450

Principal display panel and representative label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

MONOGRAM CLEANING DISPOSABLES

CLEAN FORCE

ADVANCED ANTIBACTERIAL      768071

FOAM HAND SOAP

HAND CARE

8000461

25 US FL OZ (750 mL)         H24

Active Ingredient:

Benzalkonium chloride 0.5%

771092/5402/0920

For questions or comments,

call 1-866-444-7450

Manufactured for

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

(c) 2020 Ecolab USA Inc. All rights reserved

Made in U.S.A.

Distributed by                  

US Foods Inc.

Rosemont, IL 60018 USA

representative labelrepresentative label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1731737benzalkonium chloride 0.5 % Medicated Liquid SoapPSN3
1731737benzalkonium chloride 5 MG/ML Medicated Liquid SoapSCD3
1731737benzalkonium chloride 0.5 % Medicated Liquid SoapSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47593-584-41Clean Force750 mL in 1 BOTTLE, PLASTICSOLUTION7503
47593-584-59Clean Force1250 mL in 1 BOTTLE, PLASTICSOLUTION12503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47593-584CLEAN FORCE (BENZALKONIUM CHLORIDE) SOLUTION [ECOLAB INC.]3Current NDC, Legacy NDC, 2 package rows20240805_dc7bad8c-2e29-4d5d-b87e-8d9eae7c2c1c.zip

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47593-58447593-584-41, 47593-584-59

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 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
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
METHYL GLUCETH-20J3QD0LD11PIACT
GLYCERYL MONO- AND DICAPRYLOCAPRATEU72Q2I8C85IACT
PEG-12 DIMETHICONE (300 CST)ZEL54N6W95IACT
POTASSIUM HYDROXIDEWZH3C48M4TIACT
FD&C BLUE NO. 1H3R47K3TBDIACT

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
Clean ForceBENZALKONIUM CHLORIDEEcolab Inc.dc7bad8c-2e29-4d5d-b87e-8d9eae7c2c1c2024-08-02WarningsExact identifier
ndc (package): 47593-584-59
ndc (package): 47593-584-41
ndc (product): 47593-584
ndc11 (package): 47593058441
ndc11 (package): 47593058459
spl id: 95962829-ae2f-4b3e-8f88-c9f78fbe33bc
spl set id: dc7bad8c-2e29-4d5d-b87e-8d9eae7c2c1c

Reported adverse events (FAERS/openFDA)#

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