Label: CLEAN FORCE FOAM HAND SANITIZER- benzalkonium chloride solution
- NDC Code(s): 47593-410-41
- 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 September 20, 2017
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Principal Display Panel and Representative Label
MONOGRAM™ CLEAN FORCE®
CLEANING DISPOSABLES
FOAM HAND SANITIZER
648499
Hand Care
8000180
25 FL OZ (750 mL)
H16
Active Ingredient: Benzalkonium chloride 0.1%
For questions or comments, call 1-866-444-7450.
Distributed by: © 2015 Ecolab USA Inc
PureForce All Rights Reserved
370 Wabasha Street North Made in U.S.A
St. Paul, MN 55102 755506/7100/0115
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INGREDIENTS AND APPEARANCE
CLEAN FORCE FOAM HAND SANITIZER
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47593-410 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:47593-410-41 750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/27/2003 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 10/27/2003 Labeler - Ecolab Inc. (006154611)