chloroxylenol by Vi-Jon, LLC CHLOROXYLENOL 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 and redness develop
• condition persists for more than 72 hours

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Conrol 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, isopropylideneglycerol, sodium chloride, alcohol denat., phenoxyethanol, citric acid, methylisothiazolinone, trisodium ethylenediamine disuccinate, fragrance, yellow 5, red 33

SPL UNCLASSIFIED SECTION

Do not add bleach.  Not for use in dishwashers.

​Contains Surfactants. Phosphate Free

disclaimer

This product is not manufactured or distributed by Procter & Gamble, distributor of Dawn Ultra Antibacteial Hand Soap Orange Scent

710.002/710A Rev 1

principal display panel

mountain

falls

*Compare

to Dawn

tough

on

grease

ultra

concentrated

cleaning

power

dish soap

atibacterial hand soap

orange scent

24 FL OZ (710 mL)

INGREDIENTS AND APPEARANCE

CHLOROXYLENOL 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11344-710
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	3.09 mg  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)
SOLKETAL (UNII: 3XK098O8ZW)
sodium chloride (UNII: 451W47IQ8X)
ALCOHOL (UNII: 3K9958V90M)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
trisodium ethylenediamine disuccinate (UNII: YA22H34H9Q)
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: 11344-710-50	710 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/14/2017
2	NDC: 11344-710-57	1183 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/14/2017
3	NDC: 11344-710-51	1770 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/14/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/14/2017

Labeler - Vi-Jon, Inc (150931459)

Registrant - Vi-Jon, Inc (088520668)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon, Inc		088520668	manufacture(11344-710)