FDA.reportPublic FDA data

I dont want germs on my hands (gel)

Manufacturer
Marque of Brands Americas, LLC
Effective date
2024-07-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:59:47

Label at a glance#

Productb.clean hand sanitizer
Active ingredientALCOHOL
Label structure12 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 60% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces. Rub hands together until dry
  • Supervise children under 6 years of age when using this product to avoid swallowing.

INACTIVE INGREDIENT SECTION

Water (Aqua), Aloe Barbadensis Leaf Juice, Carbomer, Fragrance, Glycerin, Propylene Glycol,Tocopheryl Acetate, Squalane

Warning

WARNINGS SECTION

  • Flammable, keep away from flame.
  • For External Use Only.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - WHEN USING SECTION

Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse throughly with water.

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - STOP USE SECTION

a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTHER SAFETY INFORMATION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73978-001B.CLEAN HAND SANITIZER (ALCOHOL) GEL [MARQUE OF BRANDS AMERICAS, LLC]2Legacy NDC20240703_a217faa1-0edb-63c0-e053-2995a90a0284.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73978-00173978-001-01, 73978-001-02, 73978-001-03, 73978-001-04

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
PROPYLENE GLYCOL6DC9Q167V3IACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
SQUALANEGW89575KF9IACT

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
3d473081-60e0-209c-e063-6394a90a863ea217faa1-0edb-63c0-e053-2995a90a02842025-08-26WarningsExact identifier
spl set id: a217faa1-0edb-63c0-e053-2995a90a0284

Reported adverse events (FAERS/openFDA)#

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