Sterno performance hand sanitizer by STERNO PRODUCTS, LLC

Sterno performance hand sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

STERNO PERFORMANCE HAND SANITIZER- alcohol solution 
STERNO PRODUCTS, LLC

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Active Ingredient

Ethanol 70% v/v. 

Purpose

Antiseptic

Use

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

• in 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 ifirritation or rash occurs. These may be signs of a serious condition.

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 oC (59-86 oF)
• Avoid freezing and excessive heat above 40 oC (104 oF)

Inactive ingredients

Propylene glycol, polyethylene glycol, acrylate polymer, distilled water, fragrance

Product label

STERNO PERFORMANCE HAND SANITIZER 
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73926-752
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
WATER (UNII: 059QF0KO0R)
RAPIDGEL EZ1 (UNII: 33JH4A7R2K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73926-752-01	8 in 1 PACKAGE	08/01/2020	12/31/2023
1		1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2	NDC: 73926-752-02	2 in 1 PACKAGE	08/01/2020	12/31/2023
2		1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3	NDC: 73926-752-03	6 in 1 PACKAGE	08/01/2020	12/31/2023
3		2000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
4	NDC: 73926-752-04	100 in 1 PACKAGE	08/01/2020	12/31/2023
4		2 mL in 1 POUCH; Type 0: Not a Combination Product
5	NDC: 73926-752-05	2000 in 1 PACKAGE	08/01/2020	12/31/2023
5		2 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	08/01/2020	12/31/2023

Labeler - STERNO PRODUCTS, LLC (117093122)

Revised: 12/2023

Document Id: 0c000212-1d43-0949-e063-6294a90a0ea0

34390-5

Set id: d406ef93-3dce-4145-a38a-db1113765632

Version: 4

Effective Time: 20231208