ENDURE 250- 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, 1%

Purpose

Healthcare personnel handwash

Uses

Healthcare personnel handwash

Warnings

For external use only

When using this product

avoid eye contact
in case of eye contact, rinse promptly and thoroughly with water

Stop use and ask doctor if

skin irritation or redness persists 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 skin and apply a small amount on hands and forearms
scrub well
rinse thoroughly and dry

Other Information

For emergency medical information in USA and Canada, call 1-800-328-0026.
For emergency medical information worldwide, call 1-651-222-5352 (in the USA).

Inactive ingredients water, potassium cocoate, propylene glycol, glycerin, potassium stearate, tetrasodium EDTA, boric acid, cocamine oxide, fragrance, isopropyl alcohol, aloe barbadensis leaf juice, FD&C blue #1, FD&C green #3, FD&C yellow #5

Questions? call 1-800-332-6522

Principal Display Panel and Representative Label

Huntington brand

25 oz

NDC 47593-244-41

DIN 02240389

ENDURE® 250

Foaming Healthcare Personnel Hand Wash

ECOLAB

890185/8501/0404

Representative label

ENDURE 250
triclosan solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47593-244
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X)	Triclosan	10.3 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
POTASSIUM COCOATE (UNII: F8U72V8ZXP)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
POTASSIUM STEARATE (UNII: 17V812XK50)
EDETATE SODIUM (UNII: MP1J8420LU)
BORIC ACID (UNII: R57ZHV85D4)
COCAMINE OXIDE (UNII: QWA2IZI6FI)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:47593-244-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/08/1999	05/05/2018

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	06/08/1999	05/05/2018

Labeler - Ecolab Inc. (006154611)

Revised: 1/2018

Document Id: f863d7f2-420d-412f-8518-4af0112d8b1c

Set id: 8408b8e5-546f-4228-b17d-7105fc32cd7a

Version: 4

Effective Time: 20180129

Ecolab Inc.