- Active ingredient
- Purpose
- Uses
- Warnings
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DOSAGE & ADMINISTRATION
Directions: Concentrated Solution
- do not mix with anything except for potable water
- use only provided bottles for diution and dispensing of ready-to-use product
- insert probe into bag, twist cap tight, and close dispenser
- fill hand soap bottle with solution from dispenser
- place bottle into a Nexa dispenser for use
Directions: Ready-To-Use Solution
- wet hands with warm water
- apply soap to hands and scrub vigorously
- wash between fingers, around fingernails, and back of hands
- rinse hands thoroughly with warm water
- dry hands with clean towel or with mechanical dryer
- Other information
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INACTIVE INGREDIENT
Ingredients (acc. INCI): water (aqua), lauryl dimethylamine oxide, cocoamidopropyl PG-dimonium chloride phosphate, glycerine, polyquaternium-77, hexylene glycol, methyl gluceth-20, PEG-7 glyceryl cocoate, tetrasodium EDTA, polyquaternium-7, lactic acid, chloro-2-methyl-4-isothiazolin-3-one, PEG-12 dimethicone. glycereth-18 ethylhexanoate, fragrance, D&C Red 33
- QUESTIONS
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Principal Display Panel and Representative Label
ECOLAB®
NDC 63146-122-11
Concentrated Foaming Antibacterial Hand Soap
FOR INSTITUTIONAL USE ONLY
Distributed by | Distribuido por:
Kay Chemical Company · 8300 Capital Drive
Greensboro NC 27409-9790 USA
Customer Service: (800) 529-5458
©2016 Kay Chemical Company
All rights reserved | Todas los derechos reservados
Made in USA | Hecho en Estados Unidos763845-00 KUSA 7+3845/8000/0116
Net contents: 2L (0.53 US Gal)
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INGREDIENTS AND APPEARANCE
ECOLAB
benzalkonium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63146-122 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE 19.8 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4) GLYCERIN (UNII: PDC6A3C0OX) POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y) HEXYLENE GLYCOL (UNII: KEH0A3F75J) METHYL GLUCETH-20 (UNII: J3QD0LD11P) PEG-7 GLYCERYL COCOATE (UNII: VNX7251543) EDETATE DISODIUM (UNII: 7FLD91C86K) LACTIC ACID (UNII: 33X04XA5AT) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) PEG-12 DIMETHICONE (UNII: ZEL54N6W95) GLYCERETH-18 ETHYLHEXANOATE (UNII: IWS58C6V2Y) D&C RED NO. 33 (UNII: 9DBA0SBB0L) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63146-122-11 2000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/18/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 02/18/2016 Labeler - Kay Chemical Company (003237021)