DIGISAN E- benzalkonium chloride solution

DigiSan E by

Drug Labeling and Warnings

DigiSan E 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
• 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

DIN 02242842

ECOLAB

23674

6123674

DigiSan™

E Foam Hand Sanitizer

750 mL (25 US FL OZ)

Active Ingredient:

Benzalkonium chloride 0.1%

706304/5404/0117

This product may be patented | Ce produit peut être breveté | Este producto puede ser

patentado: 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

© 2017 Ecolab USA Inc · All rights reserved | Tous droits réservés |

Todos los derechos reservados

Made in U.S.A. | Fabriqué aux É-U | Hecho en EE.UU.

www.ecolab.com · 706304/5404/0117

INGREDIENTS AND APPEARANCE

DIGISAN E 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-404
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: 47593-404-30	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 Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	11/04/2003

Labeler - Ecolab Inc. (006154611)