Ecochoice hand sanitizer by STERNO PRODUCTS, LLC

Ecochoice hand sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

ECOCHOICE HAND SANITIZER- alcohol liquid 
STERNO PRODUCTS, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active Ingredient                                             Purpose

Ethyl alcohol 70% v/v .................................... 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 if irritation 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 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

propylene glycol, polyethylene glycol, water, acrylate polymer

Package Label - Principal Display Panel

ECOCHOICE HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73926-778
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: 73926-778-01	8 in 1 CASE	09/01/2020	12/31/2021
1		1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2	NDC: 73926-778-02	2 in 1 PACKAGE	09/01/2020	12/31/2021
2		1000 mL in 1 PACKAGE; Type 0: Not a Combination Product
3	NDC: 73926-778-03	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/01/2020	12/31/2021
4	NDC: 73926-778-04	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/01/2020	12/31/2021
5	NDC: 73926-778-05	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	09/01/2020	12/31/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/01/2020	12/31/2021

Labeler - STERNO PRODUCTS, LLC (117093122)

Revised: 1/2022

Document Id: d657f4cb-d875-bdd8-e053-2995a90acc1d

34390-5

Set id: 0256d4e8-e097-4fb8-bf66-679283140841

Version: 2

Effective Time: 20220124