PUREFORCE- benzalkonium chloride solution

PureForce by

Drug Labeling and Warnings

PureForce 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
  

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 20 mL into hand (palmful)
• Spread to cover hands, rub in well for at least 30 seconds
• 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 1.866.444.7450

Principal Display Panel and Representative Label

Foodservice Foaming

Hand Sanitizer

Hand Care

Cuidado de las manos

Active ingredient: Benzalkonium Chloride 0.1%

766499/7100/0616

Product No.

8000340

42.3 US FL OZ (1250 mL)

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

Distributed by
PureForce
370 Wabasha Street N
St Paul MN 55102-1390 USA
© 2016 Ecolab USA Inc
All rights reserved
Made in U.S.A.

INGREDIENTS AND APPEARANCE

PUREFORCE 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-567
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: 47593-567-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/14/2016
2	NDC: 47593-567-59	1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/14/2016
3	NDC: 47593-567-30	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	06/14/2016

Labeler - Ecolab Inc. (006154611)