Label: ECOLAB- benzalkonium chloride solution
- NDC Code(s): 47593-581-41
- 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 July 18, 2023
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Representative label and principal display panel
NDC 47593-581-41
ECOLAB
Special Care
Foam Hand Sanitizer
Active Ingredient: Benzalkonium chloride 0.1%
CHG Compatible
Net Contents
25 fl oz (750 mL)
This product may be patented:
Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA · tel: 1 866 781 8787
© 2016 Ecolab USA Inc. · All rights reserved
Made in United States
769816/8500/1116
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INGREDIENTS AND APPEARANCE
ECOLAB
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47593-581 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:47593-581-41 750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/18/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 05/18/2017 Labeler - Ecolab Inc. (006154611)