GenRx Hand Sanitizing

Manufacturer
PureTek Corporation
Effective date
2024-10-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:22:31

Label at a glance#

ProductGenRx Hand Sanitizing
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Indications and uses

■ a topical antiseptic that protects against germs

Dosage and administration

■ wet hands thoroughly with product ■ allow to dry without wiping ■ repeat as necessary

Storage and handling

■ protect from freezing ■ avoid excessive heat

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

■ a topical antiseptic that protects against germs

Warnings

WARNINGS SECTION

For external use only

Do not use on

OTC - DO NOT USE SECTION

■ deep or puncture wounds ■ animal bites ■ serious burns

When using this product

OTC - WHEN USING SECTION

■ do not get into eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ Irritation and redness develop
■ condition persists for more than 72 hours

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.

Directions

DOSAGE & ADMINISTRATION SECTION

■ wet hands thoroughly with product
■ allow to dry without wiping
■ repeat as necessary

Other information

STORAGE AND HANDLING SECTION

■ protect from freezing ■ avoid excessive heat

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe barbadensis (Aloe vera) leaf juice, butylene glycol, disodium EDTA, glycerin, phenoxyethanol,

purified water, sodium hyaluronate.

GenRx Hand Sanitizing Spray (8 oz label)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039012benzalkonium chloride 0.13 % Topical SprayPSN2
1039012benzalkonium chloride 1.3 MG/ML Topical SpraySCD2
1039012benzalkonium chloride 0.13 % Topical SpraySY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59088-315-16GenRx Hand Sanitizing237 mL in 1 BOTTLE, SPRAYSPRAY2372

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59088-315GENRX HAND SANITIZING (BENZALKONIUM CHLORIDE) SPRAY [PURETEK CORPORATION]2Current NDC, Legacy NDC, 1 package rows20241004_a12715c0-77f2-7716-e053-2995a90a06d3.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59088-31559088-315-16

Ingredients#

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

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

Source Document#

Source XML · Source PDF

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
GenRx Hand SanitizingBENZALKONIUM CHLORIDEPureTek Corporationa12715c0-77f2-7716-e053-2995a90a06d32024-10-02WarningsExact identifier
ndc (package): 59088-315-16
ndc (product): 59088-315
ndc11 (package): 59088031516
spl id: 2385f398-8cf7-8437-e063-6394a90a78a4
spl set id: a12715c0-77f2-7716-e053-2995a90a06d3

Reported adverse events (FAERS/openFDA)#

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