Label: DIGISAN- alcohol aerosol, foam
- NDC Code(s): 47593-618-87
- Packager: Ecolab Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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.
Drug Label Information
Updated October 10, 2022
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
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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 120o F (48o C), puncture or incinerate
Operate only with spout pointing down - Directions
- Other Information
- INACTIVE INGREDIENT
- QUESTIONS
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Principal display panel and representative label
ECOLAB
6122644
DigiSan™ Healthcare Hand
Sanitizer Foam
425 G (15 OZ)
Active Ingredient: Ethyl alcohol 54.7% w/w (equivalent to 62.5% v/v)
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 · 720162/5403/0219
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INGREDIENTS AND APPEARANCE
DIGISAN
alcohol aerosol, foamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47593-618 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:47593-618-87 425000 mg in 1 CAN; Type 0: Not a Combination Product 10/31/2003 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 10/31/2003 Labeler - Ecolab Inc. (006154611)