FDA.reportPublic FDA data

Germ-X 721.002/721AB 99% Natural Germ-X Hand Sanitizer Spray Lavender Scent

Manufacturer
UpLift Brands, LLC | Nice-Pak Products, LLC | Chemrite Copac LLC
Effective date
2026-07-17
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
daily-update
Hydrated at
2026-07-21 05:10:10

Label at a glance#

ProductHand 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

spray 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 105°F 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 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

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • spray 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 105°F
  • may discolor some fabrics
  • harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, Aloe barbadensis leaf juice, fragrance, Rosmarinus officinalis (rosemary) leaf oil, Lavandula hybrida oil, Lavandula angustifolia (lavender) oil, linalool

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: UpLift Brands, LLC

St. Louis, MO 63114

1-888-593-0593

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

germ-X ®

SINCE 1997

LAVENDER

SCENTED

HAND

SANITIZER

KILLS 99.99% OF GERMS*

2 FL OZ (59 mL)

image descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData MatrixL0019763SBmm01.jpg

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83986-72183986-721-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
ROSEMARY OIL8LGU7VM393IACT
LAVANDIN OIL9RES347CKGIACT
LAVENDER OILZBP1YXW0H8IACT
LINALOOL, (+/-)-D81QY6I88EIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
42026-03-11full-release2026-06-01 01:49:51

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 SanitizerETHYL ALCOHOLUpLift Brands, LLCfbfa510c-2cc8-4ac8-95fc-5ac0a2e570ad2026-07-17Warnings, Adverse reactionsExact identifier
ndc (package): 83986-721-20
ndc (product): 83986-721
ndc11 (package): 83986072120
spl id: 56d1f027-9486-cd3f-e063-6394a90af112
spl set id: fbfa510c-2cc8-4ac8-95fc-5ac0a2e570ad

Reported adverse events (FAERS/openFDA)#

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