ECOCARE 360- benzalkonium solution

EcoCare 360 by

Drug Labeling and Warnings

EcoCare 360 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 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 Material Safety Data Sheet (MSDS)
• for emergency medical information in USA, call 1.800.328.0026. If located outside the United States and Canada, call collect 1.651.222.5352 (number is in the U.S.)

INACTIVE INGREDIENT

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

Questions?

Call 1.800.392.3392

Principal Display Panel - Representative Label

ECOLAB

EcoCare 360

Hand Sanitizer with Skin Conditioner

Active Ingredient: Benzalkonium Chloride 0.1%

1250 mL (42.3 flx oz)

Hand Sanitizer

Ecolab 370 Wabasha Street N St Paul MN 55102-1390 USA

tel: 1 800 392 3392

© 2014 Ecolab USA Inc All rights reserved

Made in United States

www.ecolab.com 759199/5300/1114

INGREDIENTS AND APPEARANCE

ECOCARE 360 
benzalkonium solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-275
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
ISOPROPYL ALCOHOL (UNII: ND2M416302)
WATER (UNII: 059QF0KO0R)
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: 47593-275-83	2000 mL in 1 BAG; Type 0: Not a Combination Product	02/23/1999
2	NDC: 47593-275-84	8000 mL in 1 BAG; Type 0: Not a Combination Product	02/23/1999
3	NDC: 47593-275-11	3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/23/1999
4	NDC: 47593-275-21	208000 mL in 1 DRUM; Type 0: Not a Combination Product	02/23/1999
5	NDC: 47593-275-30	207 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/23/1999
6	NDC: 47593-275-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/23/1999
7	NDC: 47593-275-56	1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/23/1999
8	NDC: 47593-275-59	1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/16/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	02/23/1999

Labeler - Ecolab Inc. (006154611)