ANTIBACTERIAL HAND WASH- benzalkonium chloride 0.13% liquid

Antibacterial Hand Wash by

Drug Labeling and Warnings

Antibacterial Hand Wash by is a Otc medication manufactured, distributed, or labeled by Vi-Jon, Inc, Vi-Jon. nc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient section

Benzalkonium chloride 0.13%

Purpose

antibacterial

Use

for handwashing to decrease bacteria on the skin

Warnings

For external use only: hands only

When using this product

• avoid contact with the eyes.  If contact occurs, rinse eyes 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, cetrimonium chloride, cocamide MEA, glycerin, lauramidopropylamine oxide, myristamidopropylamine oxide, PEG-120 methyl glucose dioleate, Punica granatum fruit extract (pomegranate), Rubus idaeus (raspberry) fruit extract, Vaccinium macrocarpon (cranberry) fruit extract, tocopheryl acetate, Camellia oleifera leaf extract (green tea), fragrance, citric acid, tetrasodium EDTA, phenoxyethanol,
methylisothiazolinone, red 33, orange 4

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

416.001/416AB

princpal display panel

mountain

falls

helps

kill harmful

germs

gentle

on skin

antibacterial

foaming

hand soap

energy berry

7.5 FL OZ (221 mL)

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL HAND WASH 
benzalkonium chloride 0.13% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11344-416
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.313 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
GLYCERIN (UNII: PDC6A3C0OX)
lauramidopropylamine oxide (UNII: I6KX160QTV)
myristamidopropylamine oxide (UNII: 3HSF539C9T)
PEG-120 methyl glucose dioleate (UNII: YM0K64F20V)
POMEGRANATE (UNII: 56687D1Z4D)
raspberry (UNII: 4N14V5R27W)
CRANBERRY (UNII: 0MVO31Q3QS)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
EDETATE SODIUM (UNII: MP1J8420LU)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
D&C ORANGE NO. 4 (UNII: Q1LIY3BO0U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11344-416-96	221 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/27/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/27/2017

Labeler - Vi-Jon, Inc (150931459)

Registrant - Vi-Jon, Inc (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon. nc		150931459	manufacture(11344-416)