719 WALNUT AVE HAND FRESH ALOE- benzalkonium chloride liquid

719 WALNUT AVE HAND by

Drug Labeling and Warnings

719 WALNUT AVE HAND by is a Otc medication manufactured, distributed, or labeled by Personal Care Products. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Factsactive ingredients

Benzalkonium Chloride

Purpose

Antiseptic

Use

hand sanitizer to help reduce bacteria on skin

Warnings

For external use only.

Flammable Keep away from heat and flame. Do not store 104°F/40°C

Stop use and ask a doctor if

irritation ot redness develops.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222).

Directions

Wet hands thoroughly with the product and rub skin until dry. Children under 6 years of age should be supervised by an adult when using.

Inactive Ingredients

Cetrimonium Chloride, Citric Acid, Dimethicone, Disodium Cocoamphodiacetate, Aloe Barbadensis Leaf Juice, Fragrance, Glycerin, Tetrasodium EDTA Water (Aqua).

719 WALNUT AVE® FOAMING HAND SANITIZER fresh aloe product label

719 WALNUT AVE®

FOAMING HAND SANITIZER
fresh aloe

2 fl OZ (60 mL)

NDC: 29500-0555-1

Distributed by:
Wal-Mart Stores, Inc.
Bentonville, AR 72716

Made in China

INGREDIENTS AND APPEARANCE

719 WALNUT AVE HAND  FRESH ALOE
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 29500-0555
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	78 mg  in 60 mL

Inactive Ingredients
Ingredient Name	Strength
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
DIMETHICONE (UNII: 92RU3N3Y1O)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE DISODIUM (UNII: 7FLD91C86K)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 29500-0555-1	60 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/19/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/19/2017

Labeler - Personal Care Products (966155082)

Registrant - Personal Care Products (966155082)