- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Other Information
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INACTIVE INGREDIENT
Inactive ingredientswater (aqua), potassium cocoate, hexylene glycol, sodium sulfate, tetrasodium EDTA, sodium lauryl sulfate, glycerin, citric acid, coco-glucoside, glyceryl oleate, fragrance, methylchloroisothiazolinone, CI 19140 (FD&C Yellow No. 5), methylisothiazolinone, CI 14700 (FD&C Red. No. 4)
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Principal Display Panel/Representative Label
NDC 63146-111-08
Kay
QSRFoaming Antibacterial Hand Soap
Jabón de manos antibacterial en espumaInstant foam lathers fast • Mild, pH-balanced formula • Fresh, clean fragrance
QSR Foaming Antibacterial Hand Soap is a rich lather hand soap with a
balanced blend of cleaning agents and skin protecting moisturizers.KEEP OUT OF REACH OF CHILDREN • FOR INSTITUTIONAL USE ONLY
Chloroxylenol 0.5%Para obtener las instrucciones en español, véase la caja exterior
Net contents: 25 US fl oz (750 ml)
Distributed by:
Kay Chemical Company · 8300 Capital Drive
Greensboro, NC 27409-9790 USA
Customer Service: (800) 529-5458
©2014 Kay Chemical Company | All rights reserved
756204-01 • KUSA 756204/8001/0214 -
INGREDIENTS AND APPEARANCE
QSR
chloroxyenol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63146-111 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) POTASSIUM COCOATE (UNII: F8U72V8ZXP) HEXYLENE GLYCOL (UNII: KEH0A3F75J) SODIUM SULFATE (UNII: 0YPR65R21J) EDETATE SODIUM (UNII: MP1J8420LU) SODIUM LAURYL SULFATE (UNII: 368GB5141J) GLYCERIN (UNII: PDC6A3C0OX) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) COCO GLUCOSIDE (UNII: ICS790225B) GLYCERYL OLEATE (UNII: 4PC054V79P) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FD&C RED NO. 4 (UNII: X3W0AM1JLX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63146-111-03 750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/22/2010 2 NDC:63146-111-08 750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/09/2013 3 NDC:63146-111-10 1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/09/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 02/22/2010 Labeler - Kay Chemical Company (003237021)