FDA.reportPublic FDA data

Germ-X D14.002/D14AC

Manufacturer
UpLift Brands LLC | Nice-Pak Products, LLC
Effective date
2026-08-11
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
daily-update
Hydrated at
2026-08-13 01:01:41

Label at a glance#

ProductAntibacterial Hand White Tea and Eucalyptus
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Dosage and administration

wet hands  apply palmful to hands  scrub thoroughly  rinse thoroughly

Label contents#

Full prescribing information#

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 with water.

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 
  • apply palmful to hands 
  • scrub thoroughly 
  • rinse thoroughly

Inactive Ingredients 

INACTIVE INGREDIENT SECTION

water, lauramine oxide, cocamidopropyl betaine, lauramidopropylamine oxide, glycerin, myristamidopropylamine oxide, fragrance, linalool, disteareth-75 IPDI, PEG-150 distearate, citric acid, sodium chloride, tetrasodium EDTA, benzophenone-4, sodium benzoate, ext. violet 2

Adverse reaction

ADVERSE REACTIONS SECTION

Formula made in USA with US and foreign components.

Distributed by: UpLift Brands, LLC

St. Louis, MO 63114

1-888-593-0593

Principal Panel Display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

germ-x

ANTIBACTERIAL

LIQUID HAND SOAP

WHITE TEA & EUCALYPTUS SCENT

Dermatologist Tested

12 FL OZ (355 mL)

image descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130198217002846GTIN-13: 0198217002846
EAN-13: 0198217002846
GTIN-12: 198217002846
UPC-A: 198217002846
GTIN storage (14 digits): 00198217002846		mm01.jpg
Data codeData MatrixL0020815SCmm01.jpg

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83986-14083986-140-32

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
LAURAMIDOPROPYLAMINE OXIDEI6KX160QTVIACT
GLYCERINPDC6A3C0OXIACT
MYRISTAMIDOPROPYLAMINE OXIDE3HSF539C9TIACT
LINALOOL, (+/-)-D81QY6I88EIACT
DISTEARETH-75 ISOPHORONE DIISOCYANATE5365FJ30SCIACT
PEG-150 DISTEARATE6F36Q0I0ACIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
SODIUM CHLORIDE451W47IQ8XIACT
EDETATE SODIUMMP1J8420LUIACT
SULISOBENZONE1W6L629B4KIACT
SODIUM BENZOATEOJ245FE5EUIACT
EXT. D&C VIOLET NO. 2G5UX3K0728IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32026-02-02full-release2026-06-01 01:36:14

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
Antibacterial Hand White Tea and EucalyptusBENZALKONIUM CHLORIDEUpLift Brands LLCff075334-501e-4f71-a563-9581a495a67b2026-08-11Warnings, Adverse reactionsExact identifier
ndc (package): 83986-140-32
ndc (product): 83986-140
ndc11 (package): 83986014032
spl id: 58c5a41c-be90-7ae3-e063-6394a90a036d
spl set id: ff075334-501e-4f71-a563-9581a495a67b

Reported adverse events (FAERS/openFDA)#

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