FDA.reportPublic FDA data

Facilipro

Manufacturer
Ecolab Inc.
Effective date
2025-04-21
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:59:28

Label at a glance#

ProductFacilipro
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 1 866 781 8787

Principal display panel and representative label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ECOLAB   6102762

FACILIPRO

Advanced Antibacterial Foaming Hand Soap

1200 mL (40.6 US FL OZ)

Active Ingredient Benzalkonium chloride 0.5%

Ecolab Inc · 1 Ecolab Place · St. Paul MN 55102 USA · tel: 1 800 35 CLEAN (352 5326)

© 2025 Ecolab USA Inc. · All rights reserved

Made in U.S.A.

783749/5400/0425

representative labelrepresentative label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1731737benzalkonium chloride 0.5 % Medicated Liquid SoapPSN4
1731737benzalkonium chloride 5 MG/ML Medicated Liquid SoapSCD4
1731737benzalkonium chloride 0.5 % Medicated Liquid SoapSY4

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
47593-566-59Facilipro1250 mL in 1 BOTTLE, PLASTICSOLUTION12504
47593-566-70Facilipro1200 mL in 1 BOTTLE, PLASTICSOLUTION12004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
47593-566FACILIPRO (BENZALKONIUM CHLORIDE) SOLUTION [ECOLAB INC.]4Current NDC, Legacy NDC, 2 package rows20250423_59580c40-ca37-4ac9-a2c3-ea86197cf68c.zip

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
47593-56647593-566-59, 47593-566-70

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
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
METHYL GLUCETH-20J3QD0LD11PIACT
GLYCERYL MONO- AND DICAPRYLOCAPRATEU72Q2I8C85IACT
ALCOHOL3K9958V90MIACT
PEG-12 DIMETHICONE (300 CST)ZEL54N6W95IACT
POTASSIUM CITRATEEE90ONI6FFIACT
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
FaciliproBENZALKONIUM CHLORIDEEcolab Inc.59580c40-ca37-4ac9-a2c3-ea86197cf68c2025-04-21WarningsExact identifier
ndc (package): 47593-566-59
ndc (package): 47593-566-70
ndc (product): 47593-566
ndc11 (package): 47593056659
ndc11 (package): 47593056670
spl id: ea4736cb-53e7-47c6-a72b-ce63e47e1d72
spl set id: 59580c40-ca37-4ac9-a2c3-ea86197cf68c

Reported adverse events (FAERS/openFDA)#

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