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 Wal-Mart, Inc, Vi-Jon, LLC, Vi-Jon. LLC. 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, glycerin, lauramine oxide, cocamidopropyl betaine, PEG-150 distearate, Punica granatum fruit extract (pomegranate), Rubus idaeus (raspberry) fruit extract, Vaccinium macrocarpon (cranberry) fruit extract, tocopheryl acetate, Camellia oleifera leaf extract (green tea), cocamide MEA, fragrance, citric acid, tetrasodium EDTA, DMDM hydantoin, benzophenone-4, red 33, orange 4

Questions?

call 1-888-287-1915

Satisfaction guaranteed

For questions or comments please call 1-888-287-1915

Satisfaction guaranteed - For questions or comments please call 1-888-287-1915

Adverse Reactions

DISTRIBUTED BY:

Wal-Mart Stores, Inc.,

Bentonville, AR 72716

416.000/416AB

principal display panel

NEW!

equate

Quality Guaranteed

Antibacterial

Foaming

Hand Wash

Energy Berry

• Helps kill harmful germs
• Gentle on sin

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: 49035-079
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)
GLYCERIN (UNII: PDC6A3C0OX)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
POMEGRANATE (UNII: 56687D1Z4D)
RASPBERRY (UNII: 4N14V5R27W)
CRANBERRY (UNII: 0MVO31Q3QS)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
EDETATE SODIUM (UNII: MP1J8420LU)
DMDM HYDANTOIN (UNII: BYR0546TOW)
SULISOBENZONE (UNII: 1W6L629B4K)
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: 49035-079-96	750 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/28/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/28/2016

Labeler - Wal-Mart, Inc (051957769)

Registrant - Vi-Jon, Inc (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon. nc		150931459	manufacture(49035-079)