CHLOROXYLENOL- chloroxylenol 0.3% liquid

Chloroxylenol by

Drug Labeling and Warnings

Chloroxylenol by is a Otc medication manufactured, distributed, or labeled by Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Chloroxylenol 0.3%

Purpose

Antibacterial

Use

 for handwashing to decrease bacteria on the skin

Warnings

For external use only: hands only

When using this product

• do not get into eyes.  If contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

• irritation or redness develops
• condition persists 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 hands
• apply palmful to hands
• scrub thoroughly
• rinse thoroughly

Inactive ingredients

water, sodium C14-16 olefin sulfonate, lauramine oxide, sodium laureth sulfate, sodium lauryl sulfate, alcohol denat., phenoxyethanol, sodium chloride, sodium xylenesulfonate, citric acid, methylisothiazolinone, fragrance, yellow 5

WARNING

Not for use in dishwasher.  Do not add bleach.

Phosphate Free.  Contains Surfactants.

adverse reactions

Manufactured by: Vi-Jon, Inc., St. Louis, MO 63114

Questions or Comments? 1-888-593-0593

Made in the USA

with US and foreign parts.

562.000/562AA

Principal display panel

mountain

falls

tough

on

grease

ultra concentrated

cleaning

power

dish soap

antibacterial hand soap

citrus scent

24 FL OZ (710 mL)

INGREDIENTS AND APPEARANCE

CHLOROXYLENOL 
chloroxylenol 0.3% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11344-562
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	3.09 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
ALCOHOL (UNII: 3K9958V90M)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11344-562-50	710 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/29/2015
2	NDC: 11344-562-68	1650 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	04/29/2015

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/29/2015

Labeler - Vi-Jon (150931459)

Registrant - Vi-Jon (088520668)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		088520668	manufacture(11344-562)