KEYSTONE ANTIBACTERIAL- triclosan solution
Ecolab Inc.

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.

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Drug Facts

Active ingredient

Triclosan, 0.3%

Purpose

Antiseptic handwash

Uses

For handwashing to decrease bacteria on the skin

Warnings

For external use only

When using this product

Discontinue use if irritation and redness develop
Avoid contact with eyes

Stop use and ask a doctor if

Irritation, discomfort and redness persist 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 with warm water
Apply handsoap
Rub vigorously for 20 seconds
Wash between fingers, around fingernails and backs of hands
Rinse thoroughly with warm water
Dry with paper towels or air-dry
Use once or twice daily as part of a daily cleaning routine

Other information

For additional information, see Material Safety Data Sheet (MSDS)
For emergency medical information in USA and Canada, cal 1-800-328-0026
For emergency medical information worldwide, call 1-651-222-5352 (in the USA)

Inactive Ingredients water, potassium cocoate, sodium laureth sulfate, SD alcohol 40-B, hexylene glycol, boric acid, hydroxyethylcellulose, cocamidopropyl PG dimonium chloride phosphate, tetrasodium EDTA, PEG 75 lanolin, lauramine oxide, fragrance, methylparaben, propylparaben, aloe barbadensis, FDC blue 1

Questions? Call 1 800 35 CLEAN

Principal Display Panel and Representative Label

KEYSTONE™

KEYSTONE ANTIBACTERIAL

LIQUID HAND SOAP

SYSCO™ 7682457

6100079 ECOLAB®

Net Contents 3.78 L (1 US gal)

Keystone is a trademark of Ecolab USA Inc.

Manufactured by:

Ecolab • 370 Wabasha Street N • St Paul MN 55102-1390 USA • tel. 1 800 352 5326

Made in United States | Hecho en EEUU • 731563/5400/0309

representative label

KEYSTONE ANTIBACTERIAL
triclosan solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47593-462
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X)	Triclosan	3 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
POTASSIUM COCOATE (UNII: F8U72V8ZXP)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
ALCOHOL (UNII: 3K9958V90M)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
BORIC ACID (UNII: R57ZHV85D4)
HYDROXYETHYL CELLULOSE (3000 CPS AT 1%) (UNII: 7Q6P4JN1QT)
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
EDETATE SODIUM (UNII: MP1J8420LU)
PEG-75 LANOLIN (UNII: 09179OX7TB)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
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:47593-462-11	3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/11/2009

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	11/11/2009	06/06/2023

Labeler - Ecolab Inc. (006154611)

Revised: 6/2023

Document Id: e8d09f99-1527-4689-87a2-d4ff37ea22d4

Set id: 3cc1b9ee-bd32-4e87-9062-3cb14db6cb86

Version: 7

Effective Time: 20230606

Ecolab Inc.