CLEAN FORCE - 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

for handwashing to decrease bacteria on the skin
recommended for repeated use

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 right away.

Directions

wet hands and forearms
dispense a palmful of product to hands
scrub hand sand forearms for 20 seconds
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

Inactive ingredients water (agua), potassium cocoate, alcohol, sodium laureth sulfate, hexylene glycol, boric acid, coccamidopropyl PG-dimonium chloride phosphate, tetrasodium EDTA, cocamine oxide, fragrance, PEG-75 lanolin, methylparaben, propylparaben, aloe barbadensis leaf juice, FD&C blue 1

Questions? call 1.866.444.7450

Principal display panel and representative label

MONOGRAM

CLEANING DISPOSABLES

CLEAN

FORCE

CLEAN FORCE

Antibacterial Foam Hand Soap

Hand Care

8000184

42.3 US FL OZ (1250 mL)

Active ingredient: Triclosan, 0.3%

For service or additional information, call 1-866-444-7450.

Distributed by:

PureForce

370 Wabasha Street North

St. Paul, MN 55102

Made in U.S.A.

755356/7100/1113

representative label

CLEAN FORCE
triclosan solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47593-391
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)
COCAMINE OXIDE (UNII: QWA2IZI6FI)
PEG-75 LANOLIN (UNII: 09179OX7TB)
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:47593-391-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/29/2004	01/07/2023
2	NDC:47593-391-59	1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/02/2013

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	07/29/2004	01/07/2023

Labeler - Ecolab Inc. (006154611)

Revised: 6/2023

Document Id: a2887cf5-88bc-4c25-9c20-f63679b86cfa

Set id: bde2a733-c63f-4f63-b2e1-5bca9b29f965

Version: 5

Effective Time: 20230606

Ecolab Inc.