PUREFORCE- chloroxylenol 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

Chloroxylenol 0.5%

Purpose

Antiseptic handwash

Uses

• For handwashing to decrease bacteria on the skin

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 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 skin and spread a small amount on hands and forearms
• scrub well, rinse thoroughly and dry

Other information

• read Safety Data Sheet (SDS) before using this product
• emergency Healthcare 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  water (aqua), potassium cocoate, hexylene glycol, sodium sulfate, tetrasodium EDTA, sodium lauryl sulfate, hydroxyethylcellulose, glycerin, cocoglucoside, glyceryl oleate, citric acid, fragrance, methylchloroisothiazolinone, methylisothiazolinone, FD&C Red #40, FD&C Yellow #5, D&C Red #33

Questions?

call 1 866 444 7450

Representative label and principal display panel

Antibacterial

Hand Soap

Hand Care

Cuidado de las manos

Active ingredient: Chloroxylenol 0.5%

Ingrediente activo: Cloroxilenol 0.5%

Product No.

8000354

1 US GAL (3.78 L)         pureFORCE

For questions or comments,

call 1-866-444-7450

Distributed by

PureForce
370 Wabasha Street North
St. Paul MN 55102 USA
© 2016 Ecolab USA Inc
All rights reserved
Made in U.S.A.
766544/7101/0716

INGREDIENTS AND APPEARANCE

PUREFORCE 
chloroxylenol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47593-571
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
POTASSIUM COCOATE (UNII: F8U72V8ZXP)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
SODIUM SULFATE (UNII: 0YPR65R21J)
EDETATE SODIUM (UNII: MP1J8420LU)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)
GLYCERIN (UNII: PDC6A3C0OX)
COCO GLUCOSIDE (UNII: ICS790225B)
GLYCERYL OLEATE (UNII: 4PC054V79P)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47593-571-11	3780 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)