Moisturizing Hand Sanitizer

Manufacturer
UpLift Brands, LLC | Nice-Pak Products, LLC
Effective date
2026-03-11
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:49:47

Label at a glance#

ProductMoisturizing Hand Sanitizer
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

Storage and handling

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

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 exterenal 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, carbomer or acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, glycerin, isopropyl myristate, tocopheryl acetate

Claims

SPL UNCLASSIFIED SECTION

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

Adverse reaction

ADVERSE REACTIONS SECTION

Distributed By Vi-Jon, LLC

St. Louis, MO 63114

www.germx.com

Principal panel display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

germ-X ®

SINCE 1997

ORIGINAL

MOISTURIZING HAND SANITIZER

Kills 99.99% of Germs*

with vitamin E

2 FL OZ (59 mL)

image descriptionimage description

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN3
581660ethanol 0.62 ML/ML Topical GelSCD3
581660ethanol 62 % Topical GelSY3

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130072785138711GTIN-13: 0072785138711
EAN-13: 0072785138711
GTIN-12: 072785138711
UPC-A: 072785138711
GTIN storage (14 digits): 00072785138711
mm02.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83986-849-08Moisturizing Hand Sanitizer3785 mL in 1 BOTTLE, PLASTICGEL37853
83986-849-16Moisturizing Hand Sanitizer59 mL in 1 BOTTLE, PLASTICGEL593
83986-849-34Moisturizing Hand Sanitizer236 mL in 1 BOTTLE, PLASTICGEL2363
83986-849-45Moisturizing Hand Sanitizer946 mL in 1 BOTTLE, PLASTICGEL9463

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83986-84983986-849-16, 83986-849-34, 83986-849-45, 83986-849-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
Moisturizing Hand SanitizerETHYL ALCOHOLUpLift Brands, LLCbf53255d-18d7-4672-8139-bacc5cb1a2e62026-03-11Warnings, Adverse reactionsExact identifier
ndc (package): 83986-849-45
ndc (package): 83986-849-34
ndc (package): 83986-849-16
ndc (package): 83986-849-08
ndc (product): 83986-849
ndc11 (package): 83986084945
ndc11 (package): 83986084916
ndc11 (package): 83986084908
ndc11 (package): 83986084934
spl id: 4cc57769-6774-9e8a-e063-6394a90a2ed4
spl set id: bf53255d-18d7-4672-8139-bacc5cb1a2e6

Reported adverse events (FAERS/openFDA)#

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