EPISOFT- 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

antibacterial hand soap

Warnings

For external use only

Do not use

In eyes

When using this product

Discontinue use if irritation and redness develop

Stop use and ask a doctor if

skin irritation or 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 skin and apply 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 and Canada, call 1-800-328-0026
for emergency medical information worldwide, cal 1-651-222-5352 (in the USA)

Inactive ingredients

water, potassium cocoate, SD alcohol 40-B, glycerin, potassium stearate, tetrasodium EDTA, cocamidopropyl PG-dimonium chloride phosphate, cocamine oxide, fragrance, methylparaben, tocopheryl acetate, citric acid, potassium hydroxide, isopropyl alcohol, propylparaben, aloe barbadensis leaf juice, FDC blue 1, FDC yellow 5

Questions?

Call 1-800-35-CLEAN (352-5326)

Principal Display Panel

NDC 47593-336-41
DIN 02242330EpiSoft
Foaming Antibacterial Lotion Soap
Turn Past click.Keep From Freezing
ECOLAB
Net Contents
25 fl oz/750 mL891300/8902/0803

Representative label

EPISOFT
triclosan solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47593-336
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)
GLYCERIN (UNII: PDC6A3C0OX)
POTASSIUM STEARATE (UNII: 17V812XK50)
EDETATE SODIUM (UNII: MP1J8420LU)
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
COCAMINE OXIDE (UNII: QWA2IZI6FI)
METHYLPARABEN (UNII: A2I8C7HI9T)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
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:47593-336-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/10/2000	04/26/2018

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	03/10/2000	04/26/2018

Labeler - Ecolab Inc. (006154611)

Revised: 2/2018

Document Id: 81b70ee6-b431-4b16-8931-b91e0b32e754

Set id: bde8f9d7-adfa-4c92-9c81-533d5d6542e0

Version: 2

Effective Time: 20180201

Ecolab Inc.