DigiSan by Ecolab Inc. Drug Facts

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]

DIGISAN  HAND SANITIZER- alcohol solution 
Ecolab Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active Ingredient

Ethyl alcohol, 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 Material Safety Data Sheet (MSDS)
• 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 lauryl lactylate, steareth-20, sodium benzoate

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

Principal display panel and representative label

ECOLAB

NDC: 47593-311-82

DigiSan

Aerosol Foam Hand Sanitizer

Active Ingredient: Ethyl alcohol 62.5% v/v

DIGITS

28432

Net Weight: 7oz/198 g

DIGISAN   HAND SANITIZER
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-311
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	54.7 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOBUTANE (UNII: BXR49TP611)
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)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-311-82	198 g in 1 CAN; Type 0: Not a Combination Product	01/10/2001	07/17/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/10/2001	07/17/2019

Labeler - Ecolab Inc. (006154611)

Registrant - Ecolab Inc. (006154611)

Revised: 7/2019

Document Id: 5f212451-33da-4b6c-be82-1c0d17a7e5db

34390-5

Set id: 87dfddfb-1f4e-406c-868e-c774e6b02d7c

Version: 4

Effective Time: 20190717

 

Ecolab Inc.