Active ingredient

Benzalkonium chloride, 0.1%

Purpose

Antiseptic handwash

Uses

for handwashing to decrease bacteria on the skin

Warnings

For external use only
Flammable, keep away from fire or flame, heat sparks and sources of static discharge

Do not use

In eyes

When using this product

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

wet hands and 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)
For emergency medical information in USA and Canada, call 1-800-328-0026
For emergency medical information worldwide, call 1-651-222-5352 (in USA)

Inactive ingredients:

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

Questions?

Call 1-800-35-CLEAN (352-5326)

Principal Display Panel/Representative Label

ECOLAB

6123674

DigiSan™

E Foam Hand Sanitizer

750 mL (25 US FL OZ)

Active Ingredient:

Benzalkonium chloride 0.1%

706304/5405/1020

This product may be patented

www.ecolab.com/patents

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

5105 Tomken Road · Mississauga ON L4W 2X5 Canada

Made in U.S.A.

www.ecolab.com

Representative Label

DIGISAN E
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47593-404
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:47593-404-30	207 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/04/2003	03/13/2017
2	NDC:47593-404-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/04/2003
3	NDC:47593-404-59	1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/04/2003	03/13/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	11/04/2003

Labeler - Ecolab Inc. (006154611)

Drug Facts