PROCLEAN FOAM NEXA HAND SANITIZER- benzalkonium chloride solution

ProClean Foam Nexa Hand Sanitizer by

Drug Labeling and Warnings

ProClean Foam Nexa Hand Sanitizer 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

Do not use

• in eyes

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

Direction

• 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)
• 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

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)

Principal display panel and representative label

ProSystem

Proclean

Foam Nexa Hand Sanitizer

Active Ingredient: Benzalkonium chloride 0.1%

6102737

750 mL

(25 US FL OZ)

Manufactured by

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

© 2024  Ecolab USA Inc. · All rights reserved

Made in U.S.A.

www.ecolab.com

INGREDIENTS AND APPEARANCE

PROCLEAN FOAM NEXA HAND SANITIZER 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-657
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 mg  in 100 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: 47593-657-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/17/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/17/2024

Labeler - Ecolab Inc. (006154611)