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Hand Sanitizer

Dosage form
SPRAY
Labeler
HS HomeWorx LLC
Label updated
2020-12-23
Retrieved
2026-09-07
Active ingredients
ALCOHOL
View original label and images on DailyMed ↗
Label information

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.

Active Ingredient(s)

Alcohol 75% v/v. Purpose: Antiseptic

Purpose

Antiseptic

Use

to help reduce bacteria on skin

Warnings

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

Label information

When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Avoid contact with broken skin. Do not inhale or ingest.

Label information

Stop use and ask a doctor if irritation or rash occurs.

Label information

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

Directions
  • Spray on hands thoroughly and rub until dry.
Other information
  • May discolor certain fabrics or surfaces.
  • Do not store above 110F (43C)
Inactive ingredients

Water (Aqua), Glycerin, Butylene Glycol, Fragrance (Parfum), Aloe Barbadensis Leaf Extract, Artemisia Argyi Leaf Extract, Cnidium Monnieri Fruit Extract, Sargassum Fusiforme Extract

Package Label - Principal Display Panel

56 mL NDC: 81282-027-01

[Image in the official label — see DailyMed source]

DailyMed Set ID: b7264eeb-7deb-44ae-e053-2995a90a48d6 · Version 1
NDC: 81282-027