Active ingredient

Triclosan 0.3%

Purpose

Antiseptic handwash

Uses

for handwashing to decrease bacteria on the skin

Warnings

For external use only

Do not use

in eyes

When using this product

if in eyes, rinse promptly and thoroughly 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 skins and apply a small amount on hands an forearms
scrub well, rinse thoroughly and dry

Other information

for additional information see, Safety Data Sheet (SDS)
for emergency medical information in USA and Canada, call 1.800.328.0026

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, FD&C blue 1

Questions? call 1.800.35.CLEAN (352.5326)

Principal display panel and representative label

KEYSTONE

ANTIBACTERIAL FOAM HANDSOAP

Triclosan 0.3%

SYSCO 0281531

6100517 ECOLAB

Net Contents: 1200 mL (40.6 US fl oz)

750767/5401/0420

Distributed by

Sysco Corporation

Manufactured by

Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA ·

tel: 1 800 35 CLEAN (352 5326)

Made in U.S.A.

representative label

KEYSTONE
triclosan solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47593-341
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:47593-341-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/26/2000	05/03/2024
2	NDC:47593-341-56	1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/26/2000

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	07/26/2000

Labeler - Ecolab Inc. (006154611)

Drug Facts