Label: CLEAN FORCE- benzalkonium chloride liquid
- NDC Code(s): 47593-586-41
- 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 May 31, 2023
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Principal display panel and representative label
MONOGRAM CLEAN FORCE
CLEANING DISPOSABLES
FOAM 917669
HAND SANITIZER
Hand Care
8000319
750 mL (25 US FL OZ) H13
Active ingredient
Benzalkonium
chloride 0.1%
771920/5400/0917
This product may be patented:
www.ecolab.com/patents
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call 1-866-444-7450
Manufactured by Distributed by
Ecolab US Foods
1 Ecolab Place Rosemont IL
St. Paul MN 55102 USA Inc 60018 USA
© 2017 Ecolab USA Inc
All rights reserved
Made in U.S.A.
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INGREDIENTS AND APPEARANCE
CLEAN FORCE
benzalkonium chloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47593-586 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:47593-586-41 750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/20/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 12/20/2017 Labeler - Ecolab Inc. (006154611)