Moisturizing Antibacterial

Manufacturer
UpLift Brands LLC | Nice-Pak Products, LLC
Effective date
2026-03-11
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:49:44

Label at a glance#

ProductMoisturizing Antibacterial
Active ingredientBENZALKONIUM CHLORIDE
Label structure13 sections

Dosage and administration

wet hands apply palmful to hands scrub thoroughly rinse thoroughly

Label contents#

Full prescribing information#

Claims

SPL UNCLASSIFIED SECTION

ANTIBACTERIAL

HAND SOAP

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

for handwashing 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 eyes thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation or 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
  • apply palmful to hands
  • scrub thoroughly
  • rinse thoroughly

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, lauramine oxide, cocamidopropyl betaine, lauramidopropylamine oxide, sodium chloride, myristamidopropylamine oxide, glycerin, fragrance, disteareth-75 IPDI, PEG-150 distearate, citric acid, tetrasodium EDTA, benzophenone-4, sodium benzoate, red 33, red 40, yellow 5

Claims

SPL UNCLASSIFIED SECTION

*Washing hands helps wash away bacteria and germs.

Adverse reaction

ADVERSE REACTIONS SECTION

DISTRIBUTED BY:

UPLIFT BRANDS, LLC

ST. LOUIS, MO 63114 

www.germx.com

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

germ-X ®

SINCE 1997

ANTIBACTERIAL

LIGHT MOISTURIZING

HAND SOAP

WASHES AWAY GERMS*

pH Balanced,

Dermatologist Tested

16 FL OZ (1 PT) 473 mL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN5
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD5
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY5
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY5

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData MatrixL0021308FBmm01.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83986-279-08Moisturizing Antibacterial3785 mL in 1 BOTTLE, PLASTICSOAP37855
83986-279-43Moisturizing Antibacterial473 mL in 1 BOTTLE, PLASTICSOAP4735

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83986-27983986-279-08, 83986-279-43

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 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 AntibacterialBENZALKONIUM CHLORIDE 0.13%UpLift Brands LLC6e42ce0e-98dd-4fd6-b307-dea66d9b3df02026-03-11Warnings, Adverse reactionsExact identifier
ndc (package): 83986-279-43
ndc (package): 83986-279-08
ndc (product): 83986-279
ndc11 (package): 83986027908
ndc11 (package): 83986027943
spl id: 4cc414c6-4edc-0860-e063-6394a90a1fca
spl set id: 6e42ce0e-98dd-4fd6-b307-dea66d9b3df0

Reported adverse events (FAERS/openFDA)#

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