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

Antispetic 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

When using this product

• if in eyes, rinse promptly and thoroughly with water
• discontinue use if irritation and rendess develop

Stop use and ask a doctor if

• eye or skin irritation or redenss 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

• for additional information, see Safety Data Sheet (SDS)
• emergency health information: 1 800 328 0026.  If located outside the United States and Canada, call collect 1 651 222 5352 (number is in the US).

INACTIVE INGREDIENT

Inactive ingredients  acrylic acid, isopropyl alcohol, myristyl alcohol, propylene glycol, triethanolamine, water (aqua)

QUESTIONS

Questions? call 1.800.444.7450

Principal Display Panel and Representative Label

Hand Sanitizer Gel

Hand Care

Cuidado de las manos

Active Ingredient: Ethanol 60% by volume

766465/7100/0616

Product No.

8000336

40.6 US FL OZ (1200 mL)

SDS-WI-15014

For questions or comments,

call 1-866-444-7450.

Distributed by
PureForce
370 Wabasha Street North
St. Paul, MN 55102
© 2016 Ecolab USA Inc
All rights reserved
Made in U.S.A.

INGREDIENTS AND APPEARANCE

PUREFORCE 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-570
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
ACRYLIC ACID (UNII: J94PBK7X8S)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
MYRISTYL ALCOHOL (UNII: V42034O9PU)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-570-56	1200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/27/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/27/2016

Labeler - Ecolab Inc. (006154611)