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 sparks and open flame

Do not use

In eyes
on deep cuts or puncture wounds

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

Eye or skin irritation and redness persist 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 and Canada, call 1.800.328.0026
for emergency medical information worldwide, call 1.651.222.5352 (in USA)

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

Questions? call 1.866.444.7450

Principal display panel and representative label

CLEAN FORCE

HAND SANITIZER

Use Clean Force 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.

Net Contents: 27 fl oz/800 mL

Product No. 8000307749811/7100/0610

Distributed by:

PureForce

370 Wabasha Street North

St. Paul, MN 55102

Made in U.S.A.

749813/7100/0610

representative label

CLEAN FORCE
ethyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47593-406
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	60 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
MYRISTYL ALCOHOL (UNII: V42034O9PU)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
TROLAMINE (UNII: 9O3K93S3TK)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:47593-406-41	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/29/2013	02/19/2024
2	NDC:47593-406-80	800 mL in 1 POUCH; Type 0: Not a Combination Product	10/27/2003

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	505G(a)(3)	10/27/2003

Labeler - Ecolab Inc. (006154611)

Drug Facts