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.

----------

Drug Facts

Active ingredient (in each use)

Chloroxylenol 0.5%

Purpose

Antiseptic handwash

Uses

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

Kay Chemical Company

representative label

CONQUEST II
chloroxylenol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:63146-201
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	0.5 mg in 100 mL

Ingredient Name	Strength
Inactive Ingredients
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 MONOOLEATE (UNII: C4YAD5F5G6)
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:63146-201-02	800 mL in 1 POUCH; Type 0: Not a Combination Product	10/13/2005	04/07/2018

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	10/13/2005	04/07/2018

Labeler - Kay Chemical Co (003237021)

Revised: 3/2018

Document Id: 5d19ac85-b64a-465b-b4a5-a7624ae51a3e

Set id: b6c8ca0e-e4e4-495b-ab7d-81feef1cfd38

Version: 2

Effective Time: 20180313

Kay Chemical Co