FDA.reportPublic FDA data

Liberty Hand Sanitizer Gel

Manufacturer
Surry Chemicals, Inc.
Effective date
2020-12-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:36:03

Label at a glance#

ProductLiberty Hand Sanitizer Gel
Active ingredientALCOHOL
Label structure12 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#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 73% 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, hydroxypropyl celluose, purified water USP

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1039.17 L NDC: 73809-8060-1

274.52 gal/1039.17 L label274.52 gal/1039.17 L label208 L NDC 73809-8060-2 55 gal/208 L label55 gal/208 L label18.93 L NDC 73809-8060-3

5 gal/18.93 L label5 gal/18.93 L label3.785L NDC 73809-8060-4 1 gal/ 3.785 L label1 gal/ 3.785 L label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2286987ethanol 73 % Topical GelPSN2
2286987ethanol 0.73 ML/ML Topical GelSCD2
2286987ethanol 73 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73809-8060-12022-01-28C16284748780-1d6a99b39-677c-a426-e053-dadaa90af4c2a22cbacf-13b7-ce85-e053-2a95a90a7aa0
73809-8060-22022-01-28C16284748780-1d6a99b39-677c-a426-e053-dadaa90af4c2a22cbacf-13b7-ce85-e053-2a95a90a7aa0
73809-8060-32022-01-28C16284748780-1d6a99b39-677c-a426-e053-dadaa90af4c2a22cbacf-13b7-ce85-e053-2a95a90a7aa0
73809-8060-42022-01-28C16284748780-1d6a99b39-677c-a426-e053-dadaa90af4c2a22cbacf-13b7-ce85-e053-2a95a90a7aa0

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73809-8060-1Liberty Hand Sanitizer Gel1039.17 L in 1 CONTAINERGEL1039.172
73809-8060-2Liberty Hand Sanitizer Gel208 L in 1 DRUMGEL2082
73809-8060-3Liberty Hand Sanitizer Gel18.93 L in 1 PAILGEL18.932
73809-8060-4Liberty Hand Sanitizer Gel3.785 L in 1 BOTTLE, PLASTICGEL3.7852

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73809-8060LIBERTY HAND SANITIZER GEL (ALCOHOL) GEL [SURRY CHEMICALS, INC.]2Legacy NDC, 4 package rows20201230_a22cbacf-13b7-ce85-e053-2a95a90a7aa0.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73809-806073809-8060-1, 73809-8060-2, 73809-8060-3, 73809-8060-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
HYDROXYPROPYL CELLULOSE, UNSPECIFIED9XZ8H6N6OHIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
b7a07493-aecd-692d-e053-2a95a90a2b9fa22cbacf-13b7-ce85-e053-2a95a90a7aa02020-12-29WarningsExact identifier
spl id: b7a07493-aecd-692d-e053-2a95a90a2b9f
spl set id: a22cbacf-13b7-ce85-e053-2a95a90a7aa0

Reported adverse events (FAERS/openFDA)#

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