PUREFORCE- alcohol 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

Ethanol 60% by volume

Purpose

Antiseptic handwash

Uses

• For handwashing to decrease bacteria on the skin

Warnings

For external use only

FLAMMABLE. Keep away from fire or flame, heat , sparks and sources of static discharge.

Do not use

• In eyes
• on deep cuts or puncture wound

When using this product

• If in eyes, rinse thoroughly with water
• Discontinue use if irritation and redness develop

Stop use and ask a doctor if

• Eye or 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

• Apply liberal amount into hand
• Spread by rubbing hands together
• Rub to dryness with attention to area around nails and between fingers

Other information

• THIS PRODUCT IS NOT A SUBSTITUTE FOR HANDWASHING WITH SOAP AND WATER
• for additional information, see Material Safety Data Sheet (MSDS)
• for emergency medical information in USA, call 1.651.222.5352

INACTIVE INGREDIENT

​Inactive ingredients​ water (aqua), isopropyl alcohol, triethanolamine, acrylates/C10-30 alkyl acrylate crosspolymer, propylene glycol, myristyl alcohol

QUESTIONS

​Questions?​ call​ 1.866.444.7450

Principal Display Panel and Representative Label

Economy

Hand Sanitizer

Active Ingredient: Ethanol 60% by volume

• Use Economy Hand Sanitizer to sanitize hands between handwashings.
• Evaporates quickly and leaves no residual fragrance.
• Leaves hands soothed and refreshed.
• Leaves no harmful or sticky residue.
• THIS PRODUCT IS NOT A SUBSTITUTE FOR SOAP AND WATER, HANDWASHING.
• FOLLOW ALL LOCAL HEALTH GUIDELINES.

8000152

Net Contents: 800 mL (27 US fl oz)

718850/7100/0712

INGREDIENTS AND APPEARANCE

PUREFORCE 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-498
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	534 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
TROLAMINE (UNII: 9O3K93S3TK)
POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
MYRISTYL ALCOHOL (UNII: V42034O9PU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-498-25	800 mL in 1 BAG; Type 0: Not a Combination Product	08/23/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/23/2012

Labeler - Ecolab Inc. (006154611)