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PureForce by Ecolab Inc.

Dosage form: solution
Ingredients: CHLOROXYLENOL 5.25mg in 1mL
Labeler: Ecolab Inc.
NDC Code: 47593-495

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.

Drug Facts

Active ingredient

Chloroxylenol 0.5%

Purpose

Antiseptic Handwash

Uses
  • For handwshing 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 irritatio and redness develop

Stop use and ask a doctof 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 ingredients​ water (aqua), potassium cocoate, hexylene glycol, sodium sulfate, tetrasodium EDTA, sodium lauryl sulfate, glycerin, citric acid, coco-glucoside, glyceryl oleate, fragrance, methylchloroisothiazolinone, CI 19140 (FDC yellow no 5), methylisothiazolinone, CI 14700 (FDC Red No 4)

​Questions?​ call​ 1.866.444.7450

Principal display panel and representative label

Economy

Antibacterial Hand Soap

Active ingredient: Chloroxylenol 0.5%

8000148

Net Content:

750 ml (25 US fl oz)

For questions or comments, call 1-866-444-7450

Distributed by:

PureForce

370 Wabasha Street North

St. Paul, MN 55102

© 2012 PureForce

All Rights Reserved

Made in U.S.A.

718617/7100/0712

PUREFORCE 
chloroxylenol solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47593-495
Route of AdministrationTopicalDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLOROXYLENOL (CHLOROXYLENOL) CHLOROXYLENOL5.25 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
water 
POTASSIUM COCOATE 
HEXYLENE GLYCOL 
SODIUM SULFATE 
EDETATE SODIUM 
SODIUM LAURYL SULFATE 
GLYCERIN 
CITRIC ACID MONOHYDRATE 
COCO GLUCOSIDE 
GLYCERYL OLEATE 
METHYLISOTHIAZOLINONE 
FD&C YELLOW NO. 5 
METHYLCHLOROISOTHIAZOLINONE 
FD&C RED NO. 4 
Packaging
#Item CodePackage Description
1NDC:47593-495-41750 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/23/2012
Labeler - Ecolab Inc. (006154611)
Establishment
NameAddressID/FEIOperations
Kay Chemical Co.003237021manufacture(47593-495), analysis(47593-495), label(47593-495), pack(47593-495), relabel(47593-495), repack(47593-495)

Revised: 08/2012
 
Ecolab Inc.

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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