KAY QSR- triclosan solution

Kay QSR by

Drug Labeling and Warnings

Kay QSR by is a Otc medication manufactured, distributed, or labeled by Kay Chemical Co.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Triclosan 0.3%

Purpose

Antiseptic handwash

Uses

• For handwashing to decrease bacteria on the skin
  

Warnings

For external use only

• In eyes
  

• If in eyes, rinse promptly and throughly with water
• Discontinue use if irritation and redness develop
  

Stop use and ask a doctor if

• Skin irritation or redness occurs for more than 72 hours
  

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Wet hands and forearms
• Dispense a palmful of product to hands
• Scrub hands and forearms for 20 seconds
• Rinse throughly and dry
  

Other Information

• for additional information, see Material Safety Data Sheet (MSDS)
• Medical Emergency: (877) 231-2615 or call collect 0 (952) 853-1713
  

INACTIVE INGREDIENT

Inactive ingredients  water (aqua), potassium cocoate, alcohol, sodium laureth sulfate, hexylene glycol, boric acid, cocamidopropyl PG-dimonium chloride phosphate, tetrasodium EDTA, cocamine oxide, fragrance, PEG-75 lanolin, methylparaben, propylparaben, aloe barbadensis leaf juice, FDC Blue 1

QUESTIONS

Questions? Call 1-800-529-5458

Principal display panel and representative label

NDC NO: 63146-118-06

KAY

QSR Anti-Bacterial

Foam Hand Soap

See inside back label for complete drug facts panel

To obtain Spanish instructions, see outer carton.

Triclosan 0.3%

40.6 US fl oz (1200 ml)

753307-00   KUSA 75330/8000/0811    copyright 2011 Kay Chemical Company   All rights reserved

INGREDIENTS AND APPEARANCE

KAY QSR 
triclosan solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63146-118
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	0.3 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
POTASSIUM COCOATE (UNII: F8U72V8ZXP)
ALCOHOL (UNII: 3K9958V90M)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
BORIC ACID (UNII: R57ZHV85D4)
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
EDETATE SODIUM (UNII: MP1J8420LU)
COCAMINE OXIDE (UNII: QWA2IZI6FI)
PEG-75 LANOLIN (UNII: 09179OX7TB)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63146-118-06	1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/30/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/30/2011

Labeler - Kay Chemical Co. (003237021)