GenRx Anti-Bacterial Gel

Manufacturer: PureTek Corporation
Effective date: 2024-10-01
Label type: HUMAN OTC DRUG LABEL
Version: 6
Source: full-release
Hydrated at: 2026-06-01 00:22:31

Label at a glance#

ProductGenRx Anti-Bacterial Gel

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.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62% (v/v)

Purpose

OTC - PURPOSE SECTION

Antiseptic

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

If irritation or rash appears and lasts.

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

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.

Other information

SPL UNCLASSIFIED SECTION

■ Do not store above 110°F (43°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis (aloe vera) Leaf Juice, Aminomethyl Propanol, Butyrospermum Parkii (Shea) Butter, Carbomer, Glycerin, Isopropyl Myristate, Water (Aqua)

GenRx Hand Sanitizing Gel (24 fl oz)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581660	ethanol 62 % Topical Gel	PSN	6
581660	ethanol 0.62 ML/ML Topical Gel	SCD	6
581660	ethanol 62 % Topical Gel	SY	6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
59088-299-08	GenRx Anti-Bacterial Gel	118 mL in 1 BOTTLE, PUMP	LIQUID	118	6
59088-299-31	GenRx Anti-Bacterial Gel	500 mL in 1 BOTTLE, DISPENSING	LIQUID	500	6
59088-299-39	GenRx Anti-Bacterial Gel	710 mL in 1 BOTTLE, PUMP	LIQUID	710	6
59088-299-48	GenRx Anti-Bacterial Gel	710 mL in 1 BOTTLE, PUMP	LIQUID	710	6

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59088-299	GENRX ANTI-BACTERIAL GEL (ALCOHOL) LIQUID [PURETEK CORPORATION]	6	Current NDC, Legacy NDC, 4 package rows	20241004_a124e37e-1a44-212a-e053-2995a90a0af0.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

GenRx Anti-Bacterial Gel
Alcohol
SHEA BUTTER
AMINOMETHYL PROPANEDIOL
ALOE VERA LEAF
GLYCERIN
CARBOMER HOMOPOLYMER TYPE C
ISOPROPYL MYRISTATE
PANTHENOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
59088-299	59088-299-48, 59088-299-08, 59088-299-31, 59088-299-39

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
Name	UNII	Kind
SHEA BUTTER	K49155WL9Y	IACT
AMINOMETHYL PROPANEDIOL	CZ7BU4QZJZ	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
GLYCERIN	PDC6A3C0OX	IACT
CARBOMER HOMOPOLYMER TYPE C	4Q93RCW27E	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
PANTHENOL	WV9CM0O67Z	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
GenRx Anti-Bacterial Gel	ALCOHOL	PureTek Corporation	a124e37e-1a44-212a-e053-2995a90a0af0	2024-10-01	Warnings	Exact identifier ndc (package): 59088-299-48 ndc (package): 59088-299-39 ndc (package): 59088-299-08 ndc (package): 59088-299-31 ndc (product): 59088-299 ndc11 (package): 59088029948 ndc11 (package): 59088029939 ndc11 (package): 59088029931 ndc11 (package): 59088029908 spl id: 23733118-0f3a-e4a8-e063-6394a90aa41e spl set id: a124e37e-1a44-212a-e053-2995a90a0af0

Reported adverse events (FAERS/openFDA)#

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