ENDURE 200- 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

Do not use

In eyes

When using this product

If skin irritation and redness occurs, discontinue use.

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 spread 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, hydroxyethylcellulose, boric acid, cocamine oxide, fragrance, isopropyl alcohol, aloe barbadensis leaf juice, FDC green 3, FDC blue 1, FDC yellow 5

Questions? Call 1-800-332-6522.

Principal Display Panel and Representative Label

Hundtington brand

NDC 47593-263-31

DIN 02239250

ENDURE® 200

Healthcare Personnel Hand Wash

Net Contents: 18 fl oz / 540 mL

Skin Synergy® Dermatology Management System

represntative label

ENDURE 200
triclosan solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47593-263
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X)	Triclosan	10.35 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)
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)
BORIC ACID (UNII: R57ZHV85D4)
COCAMINE OXIDE (UNII: QWA2IZI6FI)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:47593-263-32	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/20/1998	04/28/2018
2	NDC:47593-263-31	540 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	11/20/1998	04/28/2018

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	11/20/1998	04/28/2018

Labeler - Ecolab Inc. (006154611)

Revised: 2/2018

Document Id: 74a661d1-0955-4992-af13-e50aca9c3fa7

Set id: cf6806e3-16d0-4380-9a15-916347df4a3a

Version: 3

Effective Time: 20180219

Ecolab Inc.