CONQUEST- 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%

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, sodium lauryl sulfate, tetrasodium EDTA, sodium sulfate, hexylene glycol, hydroxyethylcellulose, glycerine, coco glucoside and glyceryl oleate, citric acid, methylchloroisothiazolinone and methylisothiazolinone, fragrance, FDC Red #40, FDC Yellow #5, DC Red #33

Questions? Call 1-800-529-5458

Principal display panel and representative label

KAY

CONQUEST

Antibacterial hand Soap

KAY

An ECOALB Company

KAY CHEMICAL COMPANY

Greensboro, NC 27409-9790, USA

27 OZ (800 ml)

722452-05

KUSA 722452/8005/0305

representative label

CONQUEST
chloroxylenol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:63146-101
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)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
EDETATE SODIUM (UNII: MP1J8420LU)
SODIUM SULFATE (UNII: 0YPR65R21J)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
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:63146-101-02	800 mL in 1 POUCH; Type 0: Not a Combination Product	10/13/2005	11/28/2019
2	NDC:63146-101-01	3800 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/13/2005	11/28/2019

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	10/13/2005	11/28/2019

Labeler - KAY CHEMICAL CO. (003237021)

Revised: 3/2018

Document Id: bf50f61c-0c8a-4b7d-8af8-c008a57a7f02

Set id: 17244a4a-6383-4df0-af89-9993e7f0e8ed

Version: 2

Effective Time: 20180312

KAY CHEMICAL CO.