Kay Qsr (Triclosan) Solution [Kay Chemical Co.] -

KAY QSR (TRICLOSAN) SOLUTION [KAY CHEMICAL CO.]
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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

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

Ingredient Name	Strength
Inactive Ingredients
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)

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

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

Labeler - Kay Chemical Co. (003237021)

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