Label: CLEAN FORCE- benzalkonium chloride solution
- NDC Code(s): 47593-584-41, 47593-584-59
- 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 February 4, 2022
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- Active Ingredient
- Purpose
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INACTIVE INGREDIENT
Inactive ingredients water (aqua), cocamine oxide, hexylene glycol, PEG-180, glycerin, cocamidopropyl , PG-dimonium chloride phosphate, phenoxyethanol, polyquaternium-7, myristamide DIPA, myristamine oxide, citric acid, methyl gluceth-20, glyceryl caprylate/caprate, alcohol, PEG-12 dimethicone, potassium citrate, fragrance, blue 1
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Principal display panel and representative label
MONOGRAM CLEANING DISPOSABLES
CLEAN FORCE
ADVANCED ANTIBACTERIAL 768067
FOAM HAND SOAP
HAND CARE
8000460
42.3 US FL OZ (1250 mL) H26
Active Ingredient:
Benzalkonium chloride 0.5%
771096/5402/0521
For questions or comments,
call 1-866-444-7450
Manufactured by
Ecolab - 1 Eclab Place
St. Paul MN 55102 USA
(c) 2021 Ecolab USA Inc.
All rights reserved
Made in U.S.A.
Distributed by
US Foods Inc.
Rosemont, IL 60018 USA
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INGREDIENTS AND APPEARANCE
CLEAN FORCE
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:47593-584 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) COCAMINE OXIDE (UNII: QWA2IZI6FI) HEXYLENE GLYCOL (UNII: KEH0A3F75J) POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B) GLYCERIN (UNII: PDC6A3C0OX) COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y) MYRISTIC DIISOPROPANOLAMIDE (UNII: 17DN142CTK) MYRISTAMINE OXIDE (UNII: J086PM3RRT) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) METHYL GLUCETH-20 (UNII: J3QD0LD11P) GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N) ALCOHOL (UNII: 3K9958V90M) PEG-12 DIMETHICONE (UNII: ZEL54N6W95) POTASSIUM CITRATE (UNII: EE90ONI6FF) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:47593-584-41 750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/30/2017 2 NDC:47593-584-59 1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/30/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 06/30/2017 Labeler - Ecolab Inc. (006154611)