DOSAGE & ADMINISTRATION SECTION.

Directions. Place enough product on hands to cover all surfaces. Rub hands together until dry.Supervise children under years of age when using this product to avoid swallowing.. Place enough product on hands to cover all surfaces. Rub hands together until dry.. Supervise children under years of age when using this product to avoid swallowing.

INACTIVE INGREDIENT SECTION.

Inactive ingredients. purified water USP.

INDICATIONS & USAGE SECTION.

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

OTC - ACTIVE INGREDIENT SECTION.

Active Ingredient(s). Sodium hypochlorite 0.015%. Purpose: Disinifecting Agent.

OTC - DO NOT USE SECTION.

Do not use. in children less than months of ageon open skin wounds. in children less than months of age. on open skin wounds.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION.

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

OTC - PURPOSE SECTION.

Purpose. Antiseptic, Hand Sanitizer.

OTC - STOP USE SECTION.

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

OTC - WHEN USING SECTION.

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 doctor if irritation or rash occurs. These may be signs of serious condition. Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL.

Package Label Principal Display Panel. 20000 mL NDC: 81436-0010-1.

SPL UNCLASSIFIED SECTION.

This is hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry. The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (80%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.Glycerol (1.45% v/v).Hydrogen peroxide (0.125% v/v).Sterile distilled water or boiled cold water.The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (80%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.. Glycerol (1.45% v/v).. Hydrogen peroxide (0.125% v/v).. Sterile distilled water or boiled cold water.

STORAGE AND HANDLING SECTION.

Other information. Store between 15-30C (59-86F)Avoid freezing and excessive heat above 40C (104F). Store between 15-30C (59-86F). Avoid freezing and excessive heat above 40C (104F).

WARNINGS SECTION.

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