KAY QSR- triclosan solution
Kay Chemical Co.

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 Facts

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 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? 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)

representative label

KAY QSR
triclosan solution

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

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	03/03/2023

Labeler - Kay Chemical Co. (003237021)

Revised: 11/2022

Document Id: 1b9c2a54-4ee9-42e6-a1f4-032b83e45b3d

Set id: eaf61ca2-35db-4d5e-88f9-e471dc142a2a

Version: 4

Effective Time: 20221114

Kay Chemical Co.