HAND WASH- benzalkonium chloride liquid

Hand Wash by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredient

Benzalkonium chloride 0.13%

PURPOSE

Antiseptic

Use

for handwashing to decrease bacteria on the skin

Warnings

For external use only: hands only

When using this product

• avoid contact with 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, cocamidopropyl betaine, lauramidopropylamine oxide, lauramine oxide, myristamidopropylamine oxide, glycerin, fragrance, citric acid, tetrasodium EDTA, benzophenone-4, sodium benzoate, red 4, yellow 5

principal display panel

mountain

falls

gentle

and mild

helps

kill harmful

gers

antibacterial

foaming

hand soap

32 FL OZ (1 QT) 946 mL

principal display panel

SIMPLY

U

GOAMING

HAND WASH

FRESH SCENT

helps kill harmful germs

7.5 FL OZ (221 mL)

INGREDIENTS AND APPEARANCE

HAND WASH 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11344-466
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)
glycerin (UNII: PDC6A3C0OX)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
EDETATE SODIUM (UNII: MP1J8420LU)
sulisobenzone (UNII: 1W6L629B4K)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11344-466-96	221 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/17/2016
2	NDC: 11344-466-44	532 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/17/2016
3	NDC: 11344-466-45	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/17/2016
4	NDC: 11344-466-03	1479 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/17/2016
5	NDC: 11344-466-57	1182 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/17/2016
6	NDC: 11344-466-08	3780 mL in 1 BOTTLE, PLASTIC; Type 1: Convenience Kit of Co-Package	02/17/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/17/2016

Labeler - Vi-Jon (150931459)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		088520668	manufacture(11344-466)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		150931459	manufacture(11344-466)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		790752542	manufacture(11344-466)