STERNO HAND SANITIZER- ethanol, isopropyl alcohol gel

Sterno Hand sanitizer by

Drug Labeling and Warnings

Sterno Hand sanitizer by is a Otc medication manufactured, distributed, or labeled by STERNO PRODUCTS, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active lngredient  

Ethanol, Isopropyl Alcohol 

Purpose 

Antiseptic

Uses 

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

Warnings  

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 product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

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

KEEP OUT OF REACH OF CHILDREN

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

Directions

• 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

Store between 15-30°C (59-86F)

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

Inactive ingredients

propylene glycol, polyethylene glycol, water

Product Label

INGREDIENTS AND APPEARANCE

STERNO HAND SANITIZER 
ethanol, isopropyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73926-738
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	63.5 mL  in 100 mL
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	2.8 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73926-738-01	3785.4 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/07/2020
2	NDC: 73926-738-02	720 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/07/2020
3	NDC: 73926-738-03	520 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/07/2020

Labeler - STERNO PRODUCTS, LLC (117093122)

Establishment
Name	Address	ID/FEI	Business Operations
STERNO PRODUCTS, LLC		004799180	manufacture(73926-738)