Neutrogel

This is a 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:

1. 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.
2. Glycerol (1.45% v/v).
3. Hydrogen peroxide (0.125% v/v).
4. 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.

Benzethonium chloride 0.10% w/w. Purpose: Antiseptic

Antiseptic

• For washing sanitizing hands
• Helps reduce bacteria on the skin that potentially can cause disease

For external use only.

• in children less than 2 months of age
• on open skin wounds

When using this product do not use

• On children less than 2 months of age
• On open skin wounds

Stop use and ask a doctor if irritation or redness persists for more than 72 hours.

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

• Wet as needed
• Place enough product in your hand
• Rub gently for at leats 30 seconds
• Wash skin, rinse thoroughly and dry

• Store at temperature below 110F (43C)

water, sodium lauryl ether sulfate, cocamidopropyl betaine, cocamide DEA, glycerin, propylene glycol, sodium chloride, citric acid, DMDM hydantoin

4000 mL NDC: 77251-008-01

200000 mL NDC: 77251-008-02

20000 mL NDC : 77251-008-03

1000 mL NDC: 77251-008-04

500 mL NDC: 77251-008-05

250 mL NDC: 77251-008-06