CONQUEST II chloroxylenol solution

United States - English - NLM (National Library of Medicine)

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Active ingredient:
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)
Available from:
Kay Chemical Co
INN (International Name):
CHLOROXYLENOL
Composition:
CHLOROXYLENOL 0.5 mL in 100 mL
Prescription type:
OTC DRUG
Authorization status:
OTC monograph not final

CONQUEST II - chloroxylenol solution

Kay Chemical Co

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they

comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredient (in each use)

Chloroxylenol 0.5%

Purpos e

Antiseptic handwash

Us es

For handwashing to decrease bacteria on the skin.

Warnings

For external use only.

When using this product

Do not get in eyes.

If contact occurs, rinse eyes thoroughly with water.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center

right away.

Directions

Wet hands and forearms.

Apply 5 ml (teaspoonful) or palmful to hands and forearms.

Scrub thoroughly for 20 seconds.

Rinse.

Repeat.

Other Information

For additional information, see Material Safety Data Sheet (MSDS)

For emergency medical information in USA call 1(800)304-0824 or call collect 0(303)592-1709

Inactive ingredients

water, potassium cocoate, hexylene glycol, sodium sulfate, tetrasodium EDTA, sodium lauryl sulfate,

hydroxyethylcellulose, glycerine, coco-glucoside and glyceryl oleate, citric acid,

methylchloroisothiazolinone and methylisothiazolinone, FDC Red #40, FDC Yellow #5, DC Red #33.

Questions? Call 1-800-529-5458

Principal display panel and representative label

KAY

CONQUEST II

Antibacterial Hand Soap

KAY

An ECOLAB Company

Kay Chemical Company

Greensboro, NC 27409-9790, USA

Customer Service: (800) 529-5458

27 OZ (800 ml)

727899-09

GDUSA 727899/8003/0405

copyright 2004, 2005

Kay Chemical Company

All Rights Reserved

CONQUEST II

chloroxylenol solution

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:6 3146 -20 1

Route of Administration

TOPICAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

CHLO RO XYLENO L (UNII: 0 F32U78 V2Q) (CHLOROXYLENOL - UNII:0 F32U78 V2Q)

CHLOROXYLENOL

0 .5 mL in 10 0 mL

Inactive Ingredients

Ingredient Name

Stre ng th

WATER (UNII: 0 59 QF0 KO0 R)

PO TASSIUM CO CO ATE (UNII: F8 U72V8 ZXP)

HEXYLENE GLYCO L (UNII: KEH0 A3F75J)

SO DIUM SULFATE (UNII: 0 YPR6 5R21J)

EDETATE SO DIUM (UNII: MP1J8 420 LU)

SO DIUM LAURYL SULFATE (UNII: 36 8 GB5141J)

HYDRO XYETHYL CELLULO SE ( 2 0 0 0 CPS AT 1%) (UNII: S38 J6 RZN16 )

GLYCERIN (UNII: PDC6 A3C0 OX)

CO CO GLUCO SIDE (UNII: ICS79 0 225B)

Kay Chemical Co

GLYCERYL MO NO O LEATE (UNII: 4PC0 54V79 P)

CITRIC ACID MO NO HYDRATE (UNII: 29 6 8 PHW8 QP)

METHYLCHLO RO ISO THIAZO LINO NE (UNII: DEL7T5QRPN)

METHYLISO THIAZO LINO NE (UNII: 229 D0 E1QFA)

FD&C RED NO . 4 0 (UNII: WZB9 127XOA)

FD&C YELLO W NO . 5 (UNII: I753WB2F1M)

D&C RED NO . 3 3 (UNII: 9 DBA0 SBB0 L)

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:6 3146 -20 1-0 2

8 0 0 mL in 1 POUCH

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

OTC mo no graph no t final

pa rt333E

10 /13/20 0 5

Labeler -

Kay Chemical Co (003237021)

Revised: 6/2011

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