EQUI-STAT- benzalkonium chloride solution 
Ecolab Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient

Benzalkonium Chloride, 0.5%

Purpose

Antiseptic handwash

Uses

for handwashing to decrease bacteria on the skin

Warnings

For external use only

Do not use

  • in eyes

When using the product

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

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

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Other information

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

Questions? call 1-866-781-8787

Principal display panel and representative label

NDC 47593-585-41 ECOLAB

EQUI-STAT ™

Antimicrobial Hand Soap

Active Ingredient: 0.5% Benzalkonium Chloride
Antimicrobial Handwash for Healthcare
CHG Compatible
Net Contents

750 mL (25 US fl oz) 6000234

This product may be patented | Este producto puede ser patentado: www.ecolab.com/patents

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

© 2017 Ecolab USA Inc. · All rights reserved | Todos los derechos reservados

Made in U.S.A. | Hecho en EE.UU.

www.ecolab.com · 771525/8500/1017

representative label

EQUI-STAT 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-585
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
COCAMINE OXIDE (UNII: QWA2IZI6FI)  
HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)  
GLYCERIN (UNII: PDC6A3C0OX)  
HYDROXYETHYL CELLULOSE (4000 MPA.S AT 1%) (UNII: ZYD53NBL45)  
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
MYRISTIC DIISOPROPANOLAMIDE (UNII: 17DN142CTK)  
MYRISTAMINE OXIDE (UNII: J086PM3RRT)  
METHYL GLUCETH-20 (UNII: J3QD0LD11P)  
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)  
ALCOHOL (UNII: 3K9958V90M)  
PEG-12 DIMETHICONE (UNII: ZEL54N6W95)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47593-585-31540 mL in 1 BOTTLE; Type 0: Not a Combination Product12/20/2017
2NDC:47593-585-591250 mL in 1 BOTTLE; Type 0: Not a Combination Product12/20/2017
3NDC:47593-585-41750 mL in 1 BOTTLE; Type 0: Not a Combination Product12/20/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E12/20/2017
Labeler - Ecolab Inc. (006154611)

Revised: 10/2022
Document Id: ae073f3f-933e-47d3-b493-693dbf4bc436
Set id: 68e3174e-cb96-4739-a723-c36b2389f4f6
Version: 3
Effective Time: 20221018
 
Ecolab Inc.