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Pureforce

Ecolab Inc.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Triclosan, 0.3%

Purpose

Antiseptic handwash

Pureforce 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 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

Pureforce 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, 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? call 1.866.444.7450

Principal display panel and representative label

PureForce Antibacterial Foam Hand Soap

Hand Care

G

Product No. 8000052

Net Contents:  25 fl oz/750 mL

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

Distributed by:

PureForce

370 Wabasha Street North

St. Paul, MN 55102

copyright 2010 PureForce

All Rights Reserved

Made in U.S.A.

705373/7100/0710

Pureforce

Pureforce

triclosan SOLUTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:47593-468
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
TRICLOSAN TRICLOSAN 0.3 mL

Inactive Ingredients

Ingredient Name Strength
water
POTASSIUM COCOATE
ALCOHOL
SODIUM LAURETH SULFATE
Hexylene Glycol
BORIC ACID
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE
EDETATE SODIUM
COCAMINE OXIDE
PEG-75 LANOLIN
METHYLPARABEN
PROPYLPARABEN
Aloe Vera Leaf
FD&C BLUE NO. 1

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:47593-468-41 750 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partE part333E 2011-03-01


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