CLEAN FORCE- triclosan solution

Clean Force by

Drug Labeling and Warnings

Clean Force by is a Otc medication manufactured, distributed, or labeled by Ecolab Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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 INGREDIENT

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

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

© 2013 Ecolab USA Inc.

All Rights Reserved

Made in U.S.A.

755356/7100/1113

INGREDIENTS AND APPEARANCE

CLEAN FORCE 
triclosan solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-391
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	0.3 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-391-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/29/2004
2	NDC: 47593-391-59	1250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	12/02/2013

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

Labeler - Ecolab Inc. (006154611)