SWISHER- benzalkonium chloride solution

Swisher by

Drug Labeling and Warnings

Swisher by is a Otc medication manufactured, distributed, or labeled by Ecolab Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium chloride 0.1%

Purpose

Antiseptic handwash

Uses

• for handwashing to decrease bacteria on the skin
  

Warnings

• For external use only
• FLAMMABLE. Keep away from fire or flame, heat, sparks, and sources of static discharge.

Do not use

• in eyes
  

When using this product

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

Stop use and ask doctor if skin irritation or redness persists 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

• wash hands to remove soil
• dispense palmful
• spread to cover hands, rub in well
• air dry, do not rinse or towel dry

Other information

• 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 USA)

INACTIVE INGREDIENT

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

QUESTIONS

Questions? call 1.800.35.CLEAN (352.5326)

Representative label and principal display panel

SWISHER

Foodservice Foaming Hand Sanitizer

Active Ingredient:  Benzalkonium chloride 0.1%

6101426

750 mL (25 US FL OZ)

Active ingredient | Benzalkonium chloride 0.1%

767264/5402/0619

This product may be patented

www.ecolab.com/patents

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

Ecolab · 1 Ecolab Place · St Paul MN 55102 USA

© 2019 Ecolab USA Inc. · All rights reserved

Made in U.S.A.

INGREDIENTS AND APPEARANCE

SWISHER 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-576
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-576-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/08/2016
2	NDC: 47593-576-30	207 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/21/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	09/08/2016

Labeler - Ecolab Inc. (006154611)