DIGISAN- alcohol solution

DigiSan by

Drug Labeling and Warnings

DigiSan by is a Otc medication manufactured, distributed, or labeled by Ecolab Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl alcohol, 54.7% w/w

(equivalent to 62.5% v/v )

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 
Contents under pressure.  Do not store at temperatures above 120 oF (48 oC), puncture or incinerate
Operate only with spout pointing down 

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

• spread thoroughly onto hands and rub until 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 the USA)

Inactive ingredients

water (aqua), isobutane, glycerin, cetearyl alcohol, hydrofluorocarbon 152A, propane, polysorbate-60, sodium lauroyl lactylate, steareth-20, sodium benzoate, tert-butyl alcohol, dentatonium benzoate

QUESTIONS

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

Principal display panel and representative label

ECOLAB

6124832

DigiSan™ Aerosol Foam Hand Sanitizer

Active Ingredient: Ethyl alcohol 54.7 w/w (eqiuvalent to 62.5% v/v)

198 G (7 OZ)

This product may be patented: www.ecolab.com/patents

SDS-MA-1396

Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA ·

tel: 1 800 35 CLEAN (352 5326)

© 2019 Ecolab USA Inc · All rights reserved

Made in U.S.A.

www.ecolab.com · 749270/5402/0219

INGREDIENTS AND APPEARANCE

DIGISAN  
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-617
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.547 mg  in 1 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOBUTANE (UNII: BXR49TP611)
GLYCERIN (UNII: PDC6A3C0OX)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)
PROPANE (UNII: T75W9911L6)
POLYSORBATE 60 (UNII: CAL22UVI4M)
SODIUM LAUROYL LACTYLATE (UNII: 7243K85WFO)
STEARETH-20 (UNII: L0Q8IK9E08)
SODIUM BENZOATE (UNII: OJ245FE5EU)
TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-617-82	198000 mg in 1 CAN; Type 0: Not a Combination Product	01/10/2001

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/10/2001

Labeler - Ecolab Inc. (006154611)