Active ingredient

Triclosan, 0.3%

Purpose

Antiseptic handwash

Uses

for handwashing to decrease bacteria on the skin

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 occurs 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 hands with warm water
Apply handsoap
Rub vigorously for 20 seconds
Wash between fingers, around fingernails and backs of hands
Rinse thoroughly with warm water
Dry with paper towels or air-dry

Other information

For additional information, see Safety Data Sheet (SDS)
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 ingredientswater (aqua), potassium cocoate, alcohol, sodium laureth sulfate, hexylene glycol, glycerin, boric acid, cocamidopropyl PG-dimonium chloride phosphate, hydroxyethylcellulose, PEG-75 lanolin, tetrasodium EDTA, cocamine oxide, fragrance, c12-15 pareth-7, methylparaben, propylparaben, sodium hydroxide, t-butyl alcohol, aloe barbadensis leaf juice, blue 1, denatonium benzoate

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

Principal display panel/Representative label

ECOLAB

10323

6110323

DigiClean™

E Hand Soap

3.78 L (1 US GAL)

This product may be patented: www.ecolab.com/patents

Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA · tel: 1 800 35 CLEAN (352 5326)

Made in U.S.A.

www.ecolab.com · 710457/5402/0317

Representative label

DIGICLEAN E
triclosan solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47593-305
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X)	Triclosan	3 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
POTASSIUM COCOATE (UNII: F8U72V8ZXP)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
ALCOHOL (UNII: 3K9958V90M)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
BORIC ACID (UNII: R57ZHV85D4)
HYDROXYETHYL CELLULOSE (3000 MPA.S AT 1%) (UNII: 7Q6P4JN1QT)
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)
EDETATE SODIUM (UNII: MP1J8420LU)
PEG-75 LANOLIN (UNII: 09179OX7TB)
COCAMINE OXIDE (UNII: QWA2IZI6FI)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:47593-305-11	3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/26/1999
2	NDC:47593-305-24	950 mL in 1 BAG; Type 0: Not a Combination Product	05/26/1999	12/18/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	05/26/1999

Labeler - Ecolab Inc. (006154611)

Drug Facts