FDA.reportPublic FDA data

Germ-X 118.001/118.401/118AE-AF

Manufacturer
UpLift Brands LLC | Nice-Pak Products, LLC
Effective date
2026-09-23
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
daily-update
Hydrated at
2026-09-25 02:00:55

Label at a glance#

ProductFoaming Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

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

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only: hands only

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes.  If contact occurs, rinse thoroughly with water.
  • avoid contact with broken skin

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • if irritation and redness develops
  • 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

Inactive ingredients

INACTIVE INGREDIENT SECTION

cetrimonium chloride, diglycerin, disodium cocoamphodiacetate, fragrance, glycerin, hydrochloric acid, methoxy PEG/PPG-7/3 aminopropyl dimethicone, sodium benzoate, tetrasodium EDTA, water

Claims

SPL UNCLASSIFIED SECTION

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

Adverse reactions

ADVERSE REACTIONS SECTION

DISTRIBUTED BY: 

UPLIFT BRANDS, LLC

ST. LOUIS, MO 63114

1-866 MY GERMX or 1-866-694-3769

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

germ-X ®

SINCE 1997

ALCOHOL FREE

FOAMING

HAND SANITIZER

Kills 99.99% of Germs*

33.8 FL OZ (1000 mL) 1.05 QT

image descriptionimage descriptionimage descriptionimage description

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
83986-11883986-118-96, 83986-118-44, 83986-118-86, 83986-118-45

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
DIGLYCERIN3YC120743UIACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
GLYCERINPDC6A3C0OXIACT
HYDROCHLORIC ACIDQTT17582CBIACT
METHOXY PEG/PPG-7/3 AMINOPROPYL DIMETHICONE4M7P1JZ2V2IACT
SODIUM BENZOATEOJ245FE5EUIACT
EDETATE SODIUMMP1J8420LUIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62026-03-11full-release2026-06-01 01:49:51
52025-11-13monthly-update2026-06-03 17:40:10

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
4cc3d5ce-f601-93a5-e063-6294a90a7296f8ca7e87-e5f1-4ef2-b389-02d318ccf78f2026-03-11Warnings, Adverse reactionsExact identifier
spl set id: f8ca7e87-e5f1-4ef2-b389-02d318ccf78f

Reported adverse events (FAERS/openFDA)#

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