GenRx Hand Sanitizing Gel with Lavender

Manufacturer
PureTek Corporation
Effective date
2024-10-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:22:32

Label at a glance#

ProductHand Sanitizing with Lavender Oil
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

■ Hand sanitizer to help reduce bacteria on the skin

Dosage and administration

■ Dispense and rub onto hands until dry. Do not rinse off. ■ Children under 6 years of age should use this product under supervision. ■ repeat as necessary

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62% (v/v)

Purpose

OTC - PURPOSE SECTION

Anti-Bacterial

Uses

INDICATIONS & USAGE SECTION

■ Hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

■ Flammable. Keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

■ do not use in or near eyes. In case of contact, rinse eyes throughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ irritation or redness develop and last 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

■ Dispense and rub onto hands until dry. Do not rinse off.

■ Children under 6 years of age should use this product under supervision.

■ repeat as necessary

Other information

SPL UNCLASSIFIED SECTION

■ Do not store above 110°F (43°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis (aloe vera) Leaf Juice, Butyrospermum Parkii (Shea) Butter, Glycerin, Lavandula Angustifolia (Lavender) Oil, Panthenol, Polyacrylate Crosspolymer-6, Water (Aqua)

GenRx Hand Sanitizing Gel with Lavender

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Manufactured in the USA by PureTek Corporation
Panorama City, CA 91402 USA
877-921-7873
www.genrxwoundcare.com

List No:41431JLA

NDC 59088-413-08

4 floz Label4 floz Label

NDC 59088-413-31

16.9 floz16.9 floz

NDC 59088-413-39

24 FLOZ24 FLOZ

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN3
581660ethanol 0.62 ML/ML Topical GelSCD3
581660ethanol 62 % Topical GelSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59088-413-06Hand Sanitizing with Lavender Oil1 in 1 KITGEL13
59088-413-08Hand Sanitizing with Lavender Oil118 mL in 1 BOTTLEGEL1183
59088-413-14Hand Sanitizing with Lavender Oil1 in 1 KITGEL13
59088-413-31Hand Sanitizing with Lavender Oil500 mL in 1 BOTTLEGEL5003
59088-413-36Hand Sanitizing with Lavender Oil1 in 1 KITGEL13
59088-413-39Hand Sanitizing with Lavender Oil710 mL in 1 BOTTLEGEL7103

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59088-413HAND SANITIZING WITH LAVENDER OIL (ALCOHOL) GEL [PURETEK CORPORATION]3Current NDC, Legacy NDC, 6 package rows20241004_a75d25a7-1e23-717f-e053-2a95a90a6d93.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59088-41359088-413-39, 59088-413-06, 59088-413-08, 59088-413-14, 59088-413-36, 59088-413-31

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

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
Hand Sanitizing with Lavender OilALCOHOLPureTek Corporationa75d25a7-1e23-717f-e053-2a95a90a6d932024-10-01WarningsExact identifier
ndc (package): 59088-413-14
ndc (package): 59088-413-31
ndc (package): 59088-413-06
ndc (package): 59088-413-39
ndc (package): 59088-413-36
ndc (package): 59088-413-08
ndc (product): 59088-413
ndc11 (package): 59088041314
ndc11 (package): 59088041308
ndc11 (package): 59088041336
ndc11 (package): 59088041339
ndc11 (package): 59088041331
ndc11 (package): 59088041306
spl id: 237334e4-0b89-c4b2-e063-6394a90a5540
spl set id: a75d25a7-1e23-717f-e053-2a95a90a6d93

Reported adverse events (FAERS/openFDA)#

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