FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
M-I L.L.C.
Effective date
2020-12-23
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:35:45

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL, ISOPROPYL ALCOHOL
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. Isopropyl Alcohol (75%, 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

Isopropyl Alcohol 75% 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

Package Label - Principal Display Panel 354 ml NDC: 75347-080-03

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Label - Principal Display Panel 354 ml NDC: 75347-080-03Package Label - Principal Display Panel 354 ml NDC: 75347-080-03Package Label - Principal Display Panel 1892 ml NDC: 75347-080-02Package Label - Principal Display Panel 1892 ml NDC: 75347-080-02Package Label - Principal Display Panel 18900 ml NDC: 75347-080-01Package Label - Principal Display Panel 18900 ml NDC: 75347-080-01Package Label - Principal Display Panel 236 ml NDC: 75347-080-04Package Label - Principal Display Panel 236 ml NDC: 75347-080-04Package Label - Principal Display Panel 236 ml NDC: 75347-075-04Package Label - Principal Display Panel 236 ml NDC: 75347-075-041892 ml_label Hand Sanitizer_75347-075-021892 ml_label Hand Sanitizer_75347-075-025 gal_Hand Sanitizer_75347-075-015 gal_Hand Sanitizer_75347-075-01354 ml NDC: 75347-075-03354 ml NDC: 75347-075-03

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039339ethanol 80 % Topical SolutionPSN4
1039900isopropyl alcohol 75 % Topical SolutionPSN4
1039339ethanol 0.8 ML/ML Topical SolutionSCD4
1039900isopropyl alcohol 0.75 ML/ML Topical SolutionSCD4
1039339ethanol 80 % Topical SolutionSY4
1039900isopropyl alcohol 75 % Topical SolutionSY4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75347-075-012022-01-28C16284748780-1d6a99b39-9a8a-a426-e053-dadaa90af4c2Hand Santizer
75347-075-032022-01-28C16284748780-1d6a99b39-9a8a-a426-e053-dadaa90af4c2Hand Santizer
75347-075-042022-01-28C16284748780-1d6a99b39-9a8a-a426-e053-dadaa90af4c2Hand Santizer
75347-075-052022-01-28C16284748780-1d6a99b39-9a8a-a426-e053-dadaa90af4c2Hand Santizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75347-075-01Hand Sanitizer18930 mL in 1 PAILLIQUID189304
75347-075-03Hand Sanitizer354 mL in 1 BOTTLELIQUID3544
75347-075-04Hand Sanitizer236 mL in 1 BOTTLELIQUID2364
75347-075-05Hand Sanitizer1892 mL in 1 BOTTLELIQUID18924
75347-080-01Hand Sanitizer18900 mL in 1 PAILLIQUID189004
75347-080-02Hand Sanitizer1892 mL in 1 BOTTLELIQUID18924
75347-080-03Hand Sanitizer354 mL in 1 BOTTLELIQUID3544
75347-080-04Hand Sanitizer236 mL in 1 BOTTLELIQUID2364

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75347-075HAND SANITIZER (ETHANOL) LIQUID HAND SANITIZER (ISOPROPYL ALCOHOL) LIQUID [M-I L.L.C.]4Legacy NDC, 4 package rows20201224_a2f36b5f-57ff-34f4-e053-2a95a90a3836.zip
75347-080HAND SANITIZER (ETHANOL) LIQUID HAND SANITIZER (ISOPROPYL ALCOHOL) LIQUID [M-I L.L.C.]4Legacy NDC, 4 package rows20201224_a2f36b5f-57ff-34f4-e053-2a95a90a3836.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75347-07575347-075-01, 75347-075-05, 75347-075-03, 75347-075-04
75347-08075347-080-01, 75347-080-02, 75347-080-03, 75347-080-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
GLYCERINPDC6A3C0OXIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302ACTIB

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
b71f1d63-b354-b056-e053-2a95a90a7792a2f36b5f-57ff-34f4-e053-2a95a90a38362020-12-23WarningsExact identifier
spl id: b71f1d63-b354-b056-e053-2a95a90a7792
spl set id: a2f36b5f-57ff-34f4-e053-2a95a90a3836

Reported adverse events (FAERS/openFDA)#

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