Hand Sanitizer
FDA Label NDC 74111-101

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):

• 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).
• Fragrance (0.200% v/v)
• Sterile distilled water or boiled cold water.

Alcohol 80% v/v. Purpose: Antiseptic

Antiseptic, Hand Sanitizer

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

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

• 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.

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.

• 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.

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

glycerin, hydrogen peroxide, fragrance, purified water USP

30 mL NDC: 74111-101-30

60 mL NDC: 74111-101-60

480 mL NDC: 74111-101-16

960 mL NDC: 74111-101-32

3785 mL NDC: 74111-101-01

9460 mL NDC: 74111-101-25

18925 mL NDC: 74111-101-05

208175 mL NDC: 74111-101-55