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Hand Sanitizer

Dosage form
CLOTH
Labeler
CARE + 1 LLC
Label updated
2020-12-14
Retrieved
2026-09-07
Active ingredients
ALCOHOL
View original label and images on DailyMed ↗
Active Ingredient(s)

Ethyl Alcohol 75% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

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

Warnings

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

Label information

When using this product

Avoid contact with eyes. In case of contact with eyes, rinse eyes thoroughly with water.

Label information

Stop use and ask a doctor if irritation or rash appears and lasts

Label information

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

Directions
  • Open lid, pull back reseable label, remove a wipe for use.
  • Reseal back after use to avoid evaporation of alcohol
Other information
  • Store between 15-30C (59-86F)
  • Dispose of wipes in the proper container
  • Do not flush down the toilet
Inactive ingredients

water (aqua), glycerin, Aloe arbadensis leaf extract (Alove Vera), Tocopheryl acetate (Vitamin E)

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:

Alcohol (75%, 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.

포장 표시

[Image in the official label — see DailyMed source]

NDC: 80072-002-10

DailyMed Set ID: b676ac2a-fbf3-ae77-e053-2a95a90a278c · Version 1
NDC: 80072-002