FDA.reportPublic FDA data

719 WALNUT AVE HAND

Manufacturer
Personal Care Products
Effective date
2017-05-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:51:40

Label at a glance#

Product719 WALNUT AVE HAND fresh aloe
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Dosage and administration

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.

Label contents#

Full prescribing information#

Drug Factsactive ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

hand sanitizer to help reduce bacteria on skin

Warnings

WARNINGS SECTION

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

OTC - STOP USE SECTION

irritation ot redness develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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

PC-WM WalnutAve FoamHand San - 555PC-WM WalnutAve FoamHand San - 555

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020365benzalkonium chloride 0.13 % Topical FoamPSN1
1020365benzalkonium chloride 1.3 MG/ML Topical FoamSCD1
1020365benzalkonium chloride 0.13 % Topical FoamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
29500-0555-12020-01-31C16284748780-19d75b9cf-febd-f424-e053-dadaa90a57cePC-WM Foaming Hand Sanitizer 0555

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
29500-0555-1719 WALNUT AVE HANDfresh aloe60 mL in 1 BOTTLE, PUMPLIQUID601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
29500-0555719 WALNUT AVE HAND FRESH ALOE (BENZALKONIUM CHLORIDE) LIQUID [PERSONAL CARE PRODUCTS]1Legacy NDC, 1 package rows20170619_9bb2133e-9f45-4635-802e-afb59a0a13b3.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
29500-055529500-0555-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
DIMETHICONE92RU3N3Y1OIACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
EDETATE DISODIUM7FLD91C86KIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
08a84a41-00bd-41f5-ab29-cc38c1151fb49bb2133e-9f45-4635-802e-afb59a0a13b32017-05-21WarningsExact identifier
spl id: 08a84a41-00bd-41f5-ab29-cc38c1151fb4
spl set id: 9bb2133e-9f45-4635-802e-afb59a0a13b3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.