PUREFORCE- benzalkonium 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 0.1%

Purpose

Antiseptic handwash

Uses

for handwashing to decrease bacteria on the skin
recommended for repeated use

Warnings

For external use only

Do not use

in eyes

When using this product

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

Sto use and ask a doctor if

skin iritation or redness occurs for more than 72 hours

Keep out of reach of children. If swallowed, get meidcal 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 infromation, see Material Safety Data Sheet (MSDS)
for emergency medical information in USA and Canada, call 1.800.328.0026

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

Questions? call 1.866.444.7450

Principal display panel and representative label

Economy

Foam Hand Sanitizer

8000149

Net Contents:

750 ml (25 US fl oz)

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

Distributed by:

PureForce

370 Wabasha Street North

St. Paul, MN 55102

Made in U.S.A.

718767/7100/0612

representative label

PUREFORCE
benzalkonium solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47593-496
Route of Administration	TOPICAL

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

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:47593-496-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/23/2012	02/16/2018

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	08/23/2012	02/16/2018

Labeler - Ecolab Inc. (006154611)

Revised: 2/2018

Document Id: 9ac5af25-1822-4733-99e8-9aa1c7b9a0c1

Set id: a687ebcc-7d29-4d92-b5a0-f4a184f8f8d3

Version: 2

Effective Time: 20180216

Ecolab Inc.