Hand Sanitizing Wipes

Manufacturer
UpLift Brands, LLC | Nice-Pak Products, LLC | DIAMOND WIPES INTERNATIONAL, INC.
Effective date
2026-03-11
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:49:48

Label at a glance#

ProductHand Sanitizing Wipes
Active ingredientALCOHOL
Label structure15 sections

Dosage and administration

wipe hands thoroughly with product and allow to dry for children under 6, use only under adult supervison not recommended for infants

Label contents#

Full prescribing information#

Claims

SPL UNCLASSIFIED SECTION

germ-x ®

SINCE 1997

ULTRA SOFT

Hand Sanitizing Wipes

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 67% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin

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

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wipe hands thoroughly with product and allow to dry
  • for children under 6, use only under adult supervison
  • not recommended for infants

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf juice, tocopheryl acetate, water

Questions?

OTC - QUESTIONS SECTION

1-866 MY GERMX   1-866-694-3769

Claims 

SPL UNCLASSIFIED SECTION

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

Side panel claims

SPL UNCLASSIFIED SECTION

TSA CARRY-ON READY

germ-X ®

SINCE 1997

ANTIBACTERIAL

Hand Sanitizing Wipes

KILLS 99.99% OF GERMS*

100 INDIVIDUALLY WRAPPED WIPES

Adverse reaction

ADVERSE REACTIONS SECTION

Distributed by: UpLift Brands, LLC

St. Louis MO 63114

1-866 MY GERMX

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TSA CARRY-ON READY

germ-X ®

Since 1997

Antibacterial

Ultra Soft

Hand Sanitizing Wipes

With Vitamin E

DO NOT FLUSH

100 Total Wipes

6 in x 5 in (15.2 cm x 12.7 cm)

Individually Wrapped Wipes

Office · School · On-The-Go

USE EVERYWHERE FOR HAND SANITIZING ON THE GO!

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2362257ethanol 67 % Medicated PadPSN4
2362257ethanol 0.67 ML/ML Medicated PadSCD4
2362257ethanol 67 % Medicated PadSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83986-100-93Hand Sanitizing Wipes3 mL in 1 PACKETCLOTH34
83986-100-93Hand Sanitizing Wipes100 in 1 BOXCLOTH1004

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83986-10083986-100-93

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
TOCOPHEROLR0ZB2556P8IACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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 WipesETHYL ALCOHOLUpLift Brands, LLCca7c6243-dc7f-40c4-8b51-ec9a7c1f14f52026-03-11Warnings, Adverse reactionsExact identifier
ndc (package): 83986-100-93
ndc (product): 83986-100
ndc11 (package): 83986010093
spl id: 4cc3be5f-1d64-7f3c-e063-6294a90a5637
spl set id: ca7c6243-dc7f-40c4-8b51-ec9a7c1f14f5

Reported adverse events (FAERS/openFDA)#

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