PUREFORCE- triclosan solution

Pureforce by

Drug Labeling and Warnings

Pureforce 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
• recommended for repeated use

Do not use

• in eyes
  

When using this product

• if in eyes, rinse promptly and throughly 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 hands and 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 (aqua), potassium cocoate, alcohol, sodium laureth sulfate, hexylene glycol, boric acid, cocamidopropyl PG-dimonium chloride phosphate, tetrasodium EDTA, cocamine oxide, fragrance, PEG-75 lanolin, methylparaben, propylparaben, aloe barbadensis leaf juice, FDC blue 1

QUESTIONS

Questions? call 1.866.444.7450

Principal display panel and representative label

PureForce Antibacterial Foam Hand Soap

Hand Care

25 FL OZ (750 mL)

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

Product No. 8000186

Distributed by:

PureForce

370 Wabasha Street North

St. Paul, MN 55102

©2013 Ecolab USA Inc.

All Rights Reserved

Made in U.S.A.

755349/7100/0713

INGREDIENTS AND APPEARANCE

PUREFORCE 
triclosan solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-564
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: 47593-564-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/03/2011

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	03/03/2011

Labeler - Ecolab Inc. (006154611)