FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
UpLift Brands, LLC | Nice-Pak Products, LLC
Effective date
2026-03-11
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:49:50

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure14 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 105⁰ F may discolor some fabrics  harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Claims

SPL UNCLASSIFIED SECTION

Paraben & Phthalate Free

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

  • 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 105⁰ F
  • may discolor some fabrics 
  • harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, PEG-6, glycerin, Glycine soja (soybean) oil, butylene glycol, Butyrospermum parkii (shea) butter, dimethicone, Aloe barbadensis leaf juice, acrylates/vinyl isodecanoate crosspolymer, fragrance, aminomethyl propanol, styrene/acrylates copolymer, xanthan gum, tocopheryl acetate

Adverse reaction

ADVERSE REACTIONS SECTION

Distributed by: UpLift Brands, LLC

St. Louis, MO 63114

1-866 MY GERMX

Disclaimer

SPL UNCLASSIFIED SECTION

*Effective at eliminating 99.9% of many common harmful germs and bacteria in as little as 15 seconds.

principal panel display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

germ-x ®

SINCE 1997

NOURISH

MOISTURIZING

HAND SANITIZER

KILLS 99.9% OF GERMS

8HR

MOISTURIZATION

with aloe & shea butter

2 FL OZ (59 mL)

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN6
581660ethanol 0.62 ML/ML Topical GelSCD6
581660ethanol 62 % Topical GelSY6

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeData MatrixL0019761BBmm02.jpg
Data codeData MatrixL0019761FBmm01.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
baf7f49c-75b6-496b-a00e-8e766a8e4f03Product name120210127
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83986-815-16Hand Sanitizer59 mL in 1 BOTTLE, PLASTICGEL596
83986-815-34Hand Sanitizer236 mL in 1 BOTTLE, PLASTICGEL2366

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83986-81583986-815-34, 83986-815-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
POLYETHYLENE GLYCOL 3005655G9Y8AQIACT
GLYCERINPDC6A3C0OXIACT
SOYBEAN OIL241ATL177AIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
SHEA BUTTERK49155WL9YIACT
DIMETHICONE92RU3N3Y1OIACT
ALOE VERA LEAFZY81Z83H0XIACT
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%)2N8MDB79NAIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
STYRENE/ACRYLAMIDE COPOLYMER (500000 MW)5Z4DPO246AIACT
XANTHAN GUMTTV12P4NEEIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
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 SanitizerETHYL ALCOHOLUpLift Brands, LLCef02b350-1a37-42d4-8eaa-38a2de5e41eb2026-03-11Warnings, Adverse reactionsExact identifier
ndc (package): 83986-815-34
ndc (package): 83986-815-16
ndc (product): 83986-815
ndc11 (package): 83986081534
ndc11 (package): 83986081516
spl id: 4cc542a7-d2e0-c06a-e063-6294a90ac71f
spl set id: ef02b350-1a37-42d4-8eaa-38a2de5e41eb

Reported adverse events (FAERS/openFDA)#

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