Sanidry

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.

Alcohol 70% v/v. Purpose: Antiseptic

Antiseptic, Hand Sanitizer

For hand sanitizing to decrease bacteria on the skin when water and soap are not available.

Recommended for repeated use.

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

• Do not use near eyes.

When using this product, do not use near eyes. If contact occurs, flush thoroughly with water.

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

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

• Remove wipes
• Rub hands together briskly until dry. No rinsing required.
• Do not reuse the towel, dispose of it immediately after use.

• Store at temperature below 110F(43C)
• Do not puncture or incinerate container

purified water USP, glycerin

Indications and Usage

Dosage and Administration

Active ingredients

Inactive ingredients

300 units NDC: 77251-006-01

[Image in the official label — see DailyMed source]