80% Alcohol Hand Sanitizer

Manufacturer
Midland Products LLC
Effective date
2020-05-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:13:57

Label at a glance#

Product80% Alcohol Hand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

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(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 80% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

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

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, hydrogen peroxide, purified water USP

WHO 80% Alcohol Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1040988.2ml label1040988.2ml label208197.6ml label208197.6ml label18927.1ml label18927.1ml label3785.4ml label3785.4ml label473.1ml label473.1ml label236.5ml label236.5ml label59ml label59ml label59mL NDC: 77136-300-02

236.5mL NDC: 77136-300-08

473.1mL NDC: 77136-300-16

3785.4 mL NDC: 77136-300-10

18927.1 mL NDC: 77136-300-05

208197.6 mL NDC: 77136-300-55

1040988.2 mL NDC: 77136-300-75

354.8ml NDC: 77136-300-12 354.8 ml label354.8 ml label

709.7ml NDC: 77136-300-24 709.7ml label709.7ml label

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77136-300-0280% Alcohol Hand Sanitizer59 mL in 1 BOTTLE, DISPENSINGLIQUID593
77136-300-0580% Alcohol Hand Sanitizer18927.1 mL in 1 PAILLIQUID18927.13
77136-300-0880% Alcohol Hand Sanitizer236.5 mL in 1 BOTTLE, DISPENSINGLIQUID236.53
77136-300-1080% Alcohol Hand Sanitizer3785.4 mL in 1 JUGLIQUID3785.43
77136-300-1280% Alcohol Hand Sanitizer354.8 mL in 1 BOTTLE, PLASTICLIQUID354.83
77136-300-1680% Alcohol Hand Sanitizer473.1 mL in 1 BOTTLE, DISPENSINGLIQUID473.13
77136-300-2480% Alcohol Hand Sanitizer709.7 mL in 1 BOTTLE, PLASTICLIQUID709.73
77136-300-5580% Alcohol Hand Sanitizer208197.6 mL in 1 DRUMLIQUID208197.63
77136-300-7580% Alcohol Hand Sanitizer1040988.2 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULKLIQUID1040988.23

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77136-30080% ALCOHOL HAND SANITIZER (ETHYL ALCOHOL HAND SANITIZER) LIQUID [MIDLAND PRODUCTS LLC]3Legacy NDC, 9 package rows20200521_a5f7246d-8c8b-1d73-e053-2995a90a2559.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
a61b798e-ce25-243c-e053-2995a90abfdfa5f7246d-8c8b-1d73-e053-2995a90a25592020-05-20WarningsExact identifier
spl id: a61b798e-ce25-243c-e053-2995a90abfdf
spl set id: a5f7246d-8c8b-1d73-e053-2995a90a2559

Reported adverse events (FAERS/openFDA)#

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