EPICARE PLUS- 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.

----------

Active ingredient

Triclosan, 0.3%

Purpose

Antiseptic handwash

Uses

for use by health care personnel in between patient contact to help reduce incidence of nosocomial infection.

Warnings

For external use only

When using this product

avoid eye contact

Stop use and ask a doctor if

irritation and 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.

Warnings

For External Use Only

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 1-651-5352 (in the USA)

Inactive ingredients

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

Questions?

Call 1-800-332-6522

Principal Display Panel/Representative Label

NDC 47593-266-24

EpiCare Plus
Antimicrobial Skin Cleanser

Net Contents: 32 fl oz/950 mL

Representative label

EPICARE PLUS
triclosan solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47593-266
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)
COCAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
POTASSIUM STEARATE (UNII: 17V812XK50)
EDETATE SODIUM (UNII: MP1J8420LU)
HYDROXYETHYL CELLULOSE (3000 CPS AT 1%) (UNII: 7Q6P4JN1QT)
COCAMINE OXIDE (UNII: QWA2IZI6FI)
METHYLPARABEN (UNII: A2I8C7HI9T)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
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:47593-266-24	950 mL in 1 POUCH; Type 0: Not a Combination Product	04/16/1999	01/30/2018

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	04/16/1999	01/30/2018

Labeler - Ecolab Inc. (006154611)

Revised: 1/2018

Document Id: 935e7c98-3093-4423-a342-9efd1fc60425

Set id: f6c745df-cfcd-4f6d-ba04-4b05b9abc1c9

Version: 2

Effective Time: 20180130

Ecolab Inc.