Germ-X D74.000/D74AB

Manufacturer
UpLift Brands LLC | Nice-Pak Products, LLC
Effective date
2026-08-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-26 01:01:18

Label at a glance#

ProductEthyl alcohol 62%
Active ingredientALCOHOL
Label structure13 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

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

SPL UNCLASSIFIED SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, ceramide NP, ceramide AP, ceramide EOP, carbomer, fragrance, isopropyl myristate, tocopheryl acetate, phytosphingosine, cholesterol, sodium lauroyl lactylate, xanthan gum, green 3

Claims

SPL UNCLASSIFIED SECTION

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

Adverse Reaction

ADVERSE REACTIONS SECTION

Distributed by: UpLift Brands, LLC

St. Louis, MO 63114

1-866 MY GERMX

^Fragrance nam only.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

germ-X ®

SINCE 1997

HYDRATING

HAND SANITIZER

EUCALYPTUS MINT^

CERAMIDES

Kills 99.99% of Germs*

2 FL OZ (59 mL)

mm01mm01mm02mm02

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83986-97483986-974-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
Ethyl alcohol 62%ETHYL ALCOHOL 62%UpLift Brands LLC5941ee9e-d109-b2be-e063-6394a90aa3232026-08-17Warnings, Adverse reactionsExact identifier
ndc (package): 83986-974-16
ndc (product): 83986-974
ndc11 (package): 83986097416
spl id: 5941ee9e-d10a-b2be-e063-6394a90aa323
spl set id: 5941ee9e-d109-b2be-e063-6394a90aa323

Reported adverse events (FAERS/openFDA)#

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