FDA.reportPublic FDA data

St Geneve Advanced Hand Sanitizer Fresh Scent

Manufacturer
4e Brands Northamerica, LLC | Global Impact Innovation LLC
Effective date
2021-03-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:49:20

Label at a glance#

ProductSt Geneve Advanced Hand Sanitizer Fresh Scent
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand sanitizer to help decrease bacteria on the skin.  When water, soap & towel are not available.  Recommended for repeated use.

Dosage and administration

Wet hands thoroughly with product. Briskly rub hands together until dry.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizer to help decrease bacteria on the skin. 
  • When water, soap & towel are not available. 
  • Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame.

Do not apply around eyes.

Do not use

OTC - DO NOT USE SECTION

in ears & mouth.

When using this product,

OTC - WHEN USING SECTION

avoid contact with eyes. In case of contact flush eyes with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if redness or irritation develop and persist for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children must be supervised in use of this product.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product. Briskly rub hands together until dry.

Other information

SPL UNCLASSIFIED SECTION

  • Store at 20°C (68° to 77°F). 
  • May discolor fabrics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Tocopheryl Acetate, Fragrance.

Questions or Comments?

OTC - QUESTIONS SECTION

Call 1-844-842-9169, M-F 8-5 CST

Package Labeling:532ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:503ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70074-65170074-651-18, 70074-651-17

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
.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
d2cd4416-b390-2570-e053-2995a90a65056f4aebf3-c7f7-4a3e-8a28-fb868113c3142021-12-10WarningsExact identifier
spl set id: 6f4aebf3-c7f7-4a3e-8a28-fb868113c314

Reported adverse events (FAERS/openFDA)#

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