Anti-Bacterial Hand Sanitizer

Manufacturer
Avon Products, Inc. | Avon Cosmetics Manofacturing, S. de R.L. de C.V.
Effective date
2023-01-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:41:23

Label at a glance#

ProductAnti-Bacterial Hand Sanitizer Blueberry
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

Hand washing to decrease bacteria on the skin. Recommended for repeated use.

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. Children under 6 should be supervised when using this product.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

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

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 64.76%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand washing to decrease bacteria on the skin. Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product

  • Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
  • Avoid contact with broken skin.

OTC - STOP USE SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and allow to dry without wiping.
  • Children under 6 should be supervised when using this product.

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER, GLYCERIN, CARBOMER, TRIETHANOLAMINE, HYDROXYPROPYLCELLULOSE, FRAGRANCE, BLUE 1

Questions?

OTC - QUESTIONS SECTION

Call 1-800-263-9746

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of PDP and Drug Facts Boximage of PDP and Drug Facts Box

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71110-001871110-0018-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
f1da48a2-2470-441b-e053-2a95a90ae584a640f325-b295-d42c-e053-2995a90a94d62023-01-09WarningsExact identifier
spl id: f1da48a2-2470-441b-e053-2a95a90ae584
spl set id: a640f325-b295-d42c-e053-2995a90a94d6

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.