SWISHER- benzalkonium chloride liquid 
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 0.1%

Purpose

Antiseptic handwash

Uses

Warnings

For external use only

Do not use

  • In eyes

When using this 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), isopropoyl alcohol, propylene glycol, FD&C red 40, FD&C blue 1

Questions? call 1.866.444.7450

Principal display panel & representative label

SWISHER

HIGH PERFORMANCE HAND SANITIZER

6101905

750 mL (25 US FL OZ)

Active ingredient: 

Benzalkonium chloride 0.1%

772419/5400/0618

For more ingredient information visit: www.ecolab.com/sds

This product may be patented: www.ecolab.com/patents

For more information visit: www.swsh.com

For questions or comments, call 1-866-444-7450.

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

© 2018 Ecolab USA Inc. · All rights reserved | Made in U.S.A. 

representative label

SWISHER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-592
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47593-592-41750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/15/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E06/15/2018
Labeler - Ecolab Inc. (006154611)

Revised: 6/2023
Document Id: 007c812c-824d-40f2-ae79-695bc8757906
Set id: 29cb072c-5273-4121-9288-2228335590e5
Version: 2
Effective Time: 20230614
 
Ecolab Inc.