DIGICLEAN SLIM-LINE- 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

Triclosan, 0.3%

Uses

Antiseptic handwash

Uses

Anti-bacterial hand soap

Warnings

For external use only

Do not use

In eyes

Discontinue use if irritation and redness develop.

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.

Directions

Wash hands and apply foam
Scrub hands and forearms
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, call 1-651-222-5352 (In USA)

Inactive ingredients water, potassium cocoate, SD alcohol 40-B, sodium laureth sulfate, hexylene glycol, boric acid, cocamidopropyl PG dimonium chloride phosphate, tetrasodium EDTA, PEG 75 lanolin, cocamine oxide, fragrance, methylparaben, propylparaben, aloe barbadensis, FDC blue 1

Questions?

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

Principal display panel and representative label

ECOLAB

NDC 47593-381-41

DIN 02246200

DigiClean Slim-Line

Anti-Bacterial Foam Hand Soap

DIGITS

24365

Net Contents: 750 mL/25 fl oz

Ecolab Inc., Institutional Division

370 Wabasha Street N., St. Paul, MN 55102-1390 U.S.A.

representative label

DIGICLEAN SLIM-LINE
triclosan solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47593-381
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)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
BORIC ACID (UNII: R57ZHV85D4)
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 (UNII: V5VD430YW9)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:47593-381-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/15/2003	02/01/2018

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	04/15/2003	02/01/2018

Labeler - Ecolab Inc. (006154611)

Revised: 2/2018

Document Id: 3315e9ab-19d2-430c-8ccc-87c7d3ed9137

Set id: a3a7d4ab-7f40-4a64-b1fc-f73e752c22c7

Version: 2

Effective Time: 20180201

Ecolab Inc.