Germ-X D69.001/D69AA

Manufacturer: UpLift Brands, LLC | Nice-Pak Products, LLC
Effective date: 2026-04-13
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-06-01 01:53:30

Label at a glance#

ProductEthyl Alcohol

Active ingredientALCOHOL

Label structure14 sections

Indications and uses

to decrease bacteria on the skin that could cause disease recommended for repeated use

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping for children under 6, use only under adult supervision not recommended for infants

Storage and handling

do not store above 105⁰F may discolor some fabrics harmful to wood finishes and plastics

Contacts and useful links#

Websitewww.germx.com

www.germx.com

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin that could cause disease
recommended for repeated use

Warnings

WARNINGS SECTION

For external use only: hands

Flammable, keep away from fire or flame.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. In case of contact with eyes, flush thoroughly with water.
avoid contact with broken skin
do not inhale or ingest

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 and allow to dry without wiping
for children under 6, use only under adult supervision
not recommended for infants

Other information

STORAGE AND HANDLING SECTION

do not store above 105⁰F
may discolor some fabrics
harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, sodium hyaluronate, carbomer, fragrance, isopropyl myristate, tocopheryl acetate

Questions?

OTC - QUESTIONS SECTION

1-866 MY GERMX

Adverse Reaction

ADVERSE REACTIONS SECTION

UpLift Brands, LLC, St. Louis, MO 63114

www.germx.com

Claims

SPL UNCLASSIFIED SECTION

*Effective at eliminating 99.99% of many common harmful germs and bacteria in as little as 15 seconds.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2 in 1

Softens & Sanitizes

germ X ^®

SINCE 1997

HYDRATING

HAND SANITIZER

WITH HYALURONIC ACID

HYALURONIC ACID

KILLS 99.99% OF GERMS*

8 FL OZ (236 mL)

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581660	ethanol 62 % Topical Gel	PSN	5
581660	ethanol 0.62 ML/ML Topical Gel	SCD	5
581660	ethanol 62 % Topical Gel	SY	5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
83986-969-16	Ethyl Alcohol	59 mL in 1 BOTTLE, PLASTIC	GEL	59	5
83986-969-34	Ethyl Alcohol	236 mL in 1 BOTTLE, PLASTIC	GEL	236	5
83986-969-86	Ethyl Alcohol	1000 mL in 1 BOTTLE, PLASTIC	GEL	1000	5

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Ethyl Alcohol
GLYCERIN
HYALURONATE SODIUM
ISOPROPYL MYRISTATE
WATER
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
.ALPHA.-TOCOPHEROL ACETATE
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
83986-969	83986-969-34, 83986-969-86, 83986-969-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
HYALURONATE SODIUM	YSE9PPT4TH	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
WATER	059QF0KO0R	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
4	2026-03-11	monthly-update	2026-06-03 17:58:43
3	2025-12-05	monthly-update	2026-06-03 17:45:27

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
Ethyl Alcohol	ETHYL ALCOHOL	UpLift Brands, LLC	289d6e34-4d71-b24e-e063-6394a90ac26d	2026-04-13	Warnings, Adverse reactions	Exact identifier ndc (package): 83986-969-16 ndc (package): 83986-969-34 ndc (package): 83986-969-86 ndc (product): 83986-969 ndc11 (package): 83986096934 ndc11 (package): 83986096986 ndc11 (package): 83986096916 spl id: 4f58eda2-ba65-b0b9-e063-6394a90a81c2 spl set id: 289d6e34-4d71-b24e-e063-6394a90ac26d

Reported adverse events (FAERS/openFDA)#

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