FDA.reportPublic FDA data

Sterno Hand sanitizer

Manufacturer
STERNO PRODUCTS, LLC
Effective date
2023-12-08
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:18:51

Label at a glance#

ProductSterno Hand sanitizer
Active ingredientALCOHOL, ISOPROPYL ALCOHOL
Label structure9 sections

Indications and uses

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

Dosage and administration

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

Label contents#

Full prescribing information#

Active lngredient  

OTC - ACTIVE INGREDIENT SECTION

Ethanol, Isopropyl Alcohol 

Purpose 

OTC - PURPOSE SECTION

Antiseptic

Uses 

INDICATIONS & USAGE SECTION

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

Warnings  

WARNINGS SECTION

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

Do not use

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

When using this productkeep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor ifirritation or rash occurs. These may be signs of a serious condition.

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.

Directions

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

Other information

SPL UNCLASSIFIED SECTION

Store between 15-30°C (59-86F)

Avoid freezing and excessive heat above 40°C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

propylene glycol, polyethylene glycol, water

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

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
73926-73873926-738-01, 73926-738-02, 73926-738-03, 73926-738-04, 73926-738-05, 73926-738-06, 73926-738-07, 73926-738-08

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
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
POLYETHYLENE GLYCOL, UNSPECIFIED3WJQ0SDW1AIACT
ALCOHOL3K9958V90MACTIB
ISOPROPYL ALCOHOLND2M416302ACTIB

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
0c000bf8-247e-d9fc-e063-6294a90aad492251ea85-4e21-40cd-bfa5-ff4eb0ef836f2023-12-08WarningsExact identifier
spl id: 0c000bf8-247e-d9fc-e063-6294a90aad49
spl set id: 2251ea85-4e21-40cd-bfa5-ff4eb0ef836f

Reported adverse events (FAERS/openFDA)#

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