FDA.reportPublic FDA data

Hand Hero Hand Sanitizer

Manufacturer
United Laboratories Manufacturing, LLC
Effective date
2023-10-25
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:23:25

Label at a glance#

ProductHand Hero Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Hand Sanitizer helps reduce bacteria on the skin that could cause disease. Recommended for repeated use.

Dosage and administration

Apply entire packet to palm of hand  Use no water or towels. Rub until hands are completely covered Agitate lightly until dry Do not rinse or wipe with towel.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70.0% v/v

Purpose

OTC - PURPOSE SECTION

Anti-Microbial

Uses

INDICATIONS & USAGE SECTION

  • Hand Sanitizer helps reduce bacteria on the skin that could cause disease.
  • Recommended for repeated use.

Warnings

WARNINGS SECTION

Flammable: Keep away from excessive heat or open flame.For external use only

When using this product

OTC - WHEN USING SECTION

  • Avoid contact with eyes. In case of eye contact flush with water.
  • Do not apply to open wounds or damaged skin.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • If accidentally swallowed or ingested, get medical help or contact poison control center immediately.
  • Do not drink. Not edible. In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Rash or irritation develops and lasts.
  • If condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply entire packet to palm of hand 
  • Use no water or towels.
  • Rub until hands are completely covered
  • Agitate lightly until dry
  • Do not rinse or wipe with towel.

Other Information

SPL UNCLASSIFIED SECTION

Storage

  • Do not store above 105 F.
  • May discolor some fabrics.
  • Harmful to wood finishes and plastics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Extract, Aminomethyl Propanol, Carbomer, Water.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62400-000462400-0004-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
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
113372a4-58da-f829-e063-6294a90a4eb1cbd38fcd-c952-46a2-b6c5-a394da82e32c2024-02-12WarningsExact identifier
spl set id: cbd38fcd-c952-46a2-b6c5-a394da82e32c

Reported adverse events (FAERS/openFDA)#

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