SOLNEXUS CHEMICAL HAND SANITIZER- ethyl alcohol 80% liquid

Solnexus Chemical Hand Sanitizer by

Drug Labeling and Warnings

Solnexus Chemical Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Agri-Empresa, Agri-Empresa, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Alcohol 80% v/v Purpose:Antiseptic

Alcohol 80% v/v Prpose: Antiseptic 33785.41 mL NDC: 76985-100-01

Glycerin Water Hydrogen Peroxide

Solnexus 1 Gal Back

Indications and Usage

Indications and Usage

When using this product:

Keep out of eyes, ears, and mouth,

In case of contact with eyes, rinse thoroughly with water

Warnings

Flammable. Keep Away from Heat and Flame

Store Between 59-86 F

For External Use Only

Dosage & Administration

Can be Used On Hands and Surfaces

OTC-Keep Out of Reach of Children

OTC-Keep Out of Reach of Children:

If Swallowed, get Medical help Promply

Purpose

Purpose:

Antiseptic

Package Label

1.041 mL NDC: 76985-100-04 208198 mL NDC: 76985-100-03

Solnexus 55 Gal 18927.1 mL NDC: 76985-100-02

Solnexus 5 Gal 3785.41 mL NDC76985-100-01

Solnexus 1 Gal

INGREDIENTS AND APPEARANCE

SOLNEXUS CHEMICAL HAND SANITIZER 
ethyl alcohol 80% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76985-100
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	80 mL  in 1000 mL

Inactive Ingredients
Ingredient Name	Strength
HYDROGEN PEROXIDE (UNII: BBX060AN9V)	0.125 mL  in 1000 mL
GLYCERIN (UNII: PDC6A3C0OX)	1.45 mL  in 1000 mL
WATER (UNII: 059QF0KO0R)	18.425 mL  in 1000 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76985-100-01	3785.41 mL in 1 BOTTLE; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)	04/08/2020
2	NDC: 76985-100-02	18927.1 mL in 1 PAIL; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)	04/08/2020
3	NDC: 76985-100-03	208198 mL in 1 DRUM; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)	04/08/2020
4	NDC: 76985-100-04	1.014 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)	04/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/08/2020

Labeler - Agri-Empresa (080291566)

Establishment
Name	Address	ID/FEI	Business Operations
Agri-Empresa, LLC		080291566	manufacture(76985-100)