Conquest by KAY CHEMICAL CO. Drug Facts

Conquest by

Drug Labeling and Warnings

Conquest by is a Otc medication manufactured, distributed, or labeled by KAY CHEMICAL CO.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

copyright 2004, 2005 Kay Chemical Company All Rights Reserved

CONQUEST 
chloroxylenol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63146-101
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
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 Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
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

34390-5

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

Version: 2

Effective Time: 20180312