ANTIBACTERIAL- chloroxylenol liquid

antibacterial by

Drug Labeling and Warnings

antibacterial 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., fragrance, phenoxyethanol, citric acid, methylisothiazolinone, trisodium ethylenediamine disuccinate, yellow 5, blue 1

adverse reactions section

*This product is not manufactured or distributed by Procter & Gamble, distributor of Dawn Ultra Antibacterial Hand Soap Apple Blossom Scent

Do not add bleach.  Not for use in dishwashers.

Contains surfactants.  Phosphate-free formula.

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

Questions or comments?  1-888-593-0593

Made in the USA with US and foreign components

principal display panel

mountain

falls

*Compare to Dawn

tough on grease

ultra concentrated cleaning power

dish soap

antibacterial hand soap

crisp apple scent

90 FL OZ (2.66 L)

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11344-713
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	3 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)
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)
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)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11344-713-44	532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/14/2017
2	NDC: 11344-713-50	710 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/14/2017
3	NDC: 11344-713-04	1040 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/14/2017
4	NDC: 11344-713-57	1183 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/14/2017
5	NDC: 11344-713-68	1650 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/14/2017
6	NDC: 11344-713-51	1770 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/14/2017
7	NDC: 11344-713-90	2662 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(11344-713)