PURE FORCE- benzalkonium chloride liquid

Pure Force by

Drug Labeling and Warnings

Pure Force 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
• recommended for repeated use

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

• 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 Material Safety Data Sheet (MSDS)
• for emergency medical information in USA, call 1.800.328.0026

INACTIVE INGREDIENT

Inactive ingredients  water (aqua), isopropoyl alcohol, propylene glycol, FDC red 40, FDC blue 1

QUESTIONS

Questions? call 1.866.444.7450

Principal Display Panel with Representative Label

Hand Sanitizing Foam

Active ingredient:  Benzalkonium chloride 0.1%

25 FL OZ (750 mL)

Pure Force™

Distributed by:                        © 2013 Ecolab USA Inc.

PureForce                               All Rights Reserved

370 Wabasha Street North       Made in U.S.A.

St. Paul, MN 55102                           755509/7100/0713

INGREDIENTS AND APPEARANCE

PURE FORCE 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-504
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: 47593-504-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/28/2013
2	NDC: 47593-504-59	1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/28/2013	09/28/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/28/2013

Labeler - Ecolab Inc. (006154611)