ENDURE 100- 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, 0.2%

Purpose

Antiseptic hand wash

Uses

for hand washing 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 immediately.

Directions

wet skin and spread a small amount on hands and forearms
scrub well, rinse thoroughly and dry

Other information

for additional information, see Material Safety Data Sheet (MSDS)
for emergency medical information in USA, call 1.800.328.0026

Inactive ingredients water (aqua), potassium cocoate, SD alcohol, potassium stearate, glycerin, boric acid, cocamidopropyl PG-dimonium chloride phosphate, hydroxyethylcellulose, tetrasodium EDTA, cocamine oxide, PEG-75 lanolin, methylparaben, propylparaben, fragrance, aloe barbadensis leaf juice, FDC green 3

Questions? call 1.866.781.8787

Principal Display Panel and Representative Label

ECOLAB

NDC 47593-262-32

ENDURE® 100

Antibacterial Skin Cleaner

Active Ingredient: 0.2% Triclosan

Net Contents: 1000 mL (33.8 fl oz)

61430146

represntative label

ENDURE 100
triclosan solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47593-262
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X)	Triclosan	2.05 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
POTASSIUM COCOATE (UNII: F8U72V8ZXP)
ALCOHOL (UNII: 3K9958V90M)
POTASSIUM STEARATE (UNII: 17V812XK50)
GLYCERIN (UNII: PDC6A3C0OX)
BORIC ACID (UNII: R57ZHV85D4)
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)
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 GREEN NO. 3 (UNII: 3P3ONR6O1S)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:47593-262-32	1000 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: 1/2018

Document Id: b539693d-596b-404f-823d-008b28f17d6d

Set id: 1516c1f3-cbeb-4e3d-8ad9-8abae2015c3e

Version: 3

Effective Time: 20180129

Ecolab Inc.