FDA.reportPublic FDA data

PureForce

Manufacturer
Ecolab Inc.
Effective date
2025-12-30
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:29:13

Label at a glance#

ProductPureForce
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

For handwashing to decrease bacteria on the skin

Dosage and administration

Wash hands to remove soil dispense 20 mL into hand (palmful) spread to cover hands, rub in well for at least 30 seconds air dry, do not rinse or towel dry

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride, 0.1%

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 this product

OTC - WHEN USING SECTION

  • Discontinue use if irritation and redness develop

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if skin irritation and redness develop

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

  • Wash hands to remove soil
  • dispense 20 mL into hand (palmful)
  • spread to cover hands, rub in well for at least 30 seconds
  • air dry, do not rinse or towel dry

Other information

REFERENCES SECTION

  • for additional information, see Safety Data Sheet (SDS)
  • for emergency medical information in USA and Canada, call 1-800-328-0026
  • for emergency medical information worldwide, call 1-651-222-5352 (in the USA)

INACTIVE INGREDIENT SECTION

Inactive ingredients water (aqua), isopropyl alcohol, propylene glycol, FD&C red 40, FD&C blue 1

OTC - QUESTIONS SECTION

Questions? call 1-866-444-7450

Principal Display Panel and Representative Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Foodservice Foaming

Hand Sanitizer

Hand Care

Active ingredient: Benzalkonium Chloride 0.1%

Product No.

8000360

25 US FL OZ

(750 mL)

766561/5401/1021

For questions or comments,

call 1-866-444-7450.

Distributed by
Ecolab

1 Ecolab Place

St Paul MN 55102 USA

© 2021 Ecolab USA Inc

All rights reserved

Made in U.S.A.

representative labelrepresentative label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038791benzalkonium chloride 0.1 % Topical SolutionPSN5
1038791benzalkonium chloride 1 MG/ML Topical SolutionSCD5
1038791benzalkonium chloride 0.1 % Topical SolutionSY5

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
47593-567-30PureForce207 mL in 1 BOTTLE, PLASTICSOLUTION2075
47593-567-41PureForce750 mL in 1 BOTTLE, PLASTICSOLUTION7505
47593-567-59PureForce1250 mL in 1 BOTTLE, PLASTICSOLUTION12505

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47593-56747593-567-41, 47593-567-59, 47593-567-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
FD&C RED NO. 40WZB9127XOAIACT
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
PureForceBENZALKONIUM CHLORIDEEcolab Inc.4c2bcf98-a2c8-48ee-a3e0-e49cb667b27e2025-12-30WarningsExact identifier
ndc (package): 47593-567-41
ndc (package): 47593-567-59
ndc (package): 47593-567-30
ndc (product): 47593-567
ndc11 (package): 47593056730
ndc11 (package): 47593056741
ndc11 (package): 47593056759
spl id: 2b024278-ada2-4425-9502-2a6fa4e9e94d
spl set id: 4c2bcf98-a2c8-48ee-a3e0-e49cb667b27e

Reported adverse events (FAERS/openFDA)#

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