Hand Sanitizer

Manufacturer
Virus Protection Systems LLC
Effective date
2020-05-18
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:13:33

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping

Storage and handling

Not Tested on Animals

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% - Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

for hand-washing to decrease bacteria on the skin, only when water is not available

Warnings

WARNINGS SECTION

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

OTC - WHEN USING SECTION

When using this product keep do not get into the eyes, ears, and mouth. If contact occurs rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or redness develop

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 and redness develop

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

Other information

STORAGE AND HANDLING SECTION

Not Tested on Animals

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin Fragrance, Carbomer, Triethanolamine, Denatonium Benzoate

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

On the go protection

Antiseptic Antibacterial

Hand Sanitizer

No Water Required

70% Alcohol

Non Sterile Solution

30 mL

Full Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Full LabelFull Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN2
582753ethanol 0.7 ML/ML Topical SolutionSCD2
582753ethanol 70 % Topical SolutionSY2
582753ethyl alcohol 70 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74707-001-012022-01-28C16284748780-1d6a99b39-d9d7-a426-e053-dadaa90af4c2Hand Sanitizer 30ML
74707-001-022022-01-28C16284748780-1d6a99b39-d9d7-a426-e053-dadaa90af4c2Hand Sanitizer 30ML

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74707-001-01Hand Sanitizer30 mL in 1 BOTTLE, PLASTICLIQUID302
74707-001-02Hand Sanitizer30 mL in 1 BOTTLE, PLASTICLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74707-001HAND SANITIZER (ALCOHOL) LIQUID [VIRUS PROTECTION SYSTEMS LLC]2Legacy NDC, 2 package rows20200519_a3377c80-1ac6-7160-e053-2a95a90a395c.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
74707-00174707-001-01, 74707-001-02

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 · Source PDF

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
a5f683d3-8db1-1a28-e053-2995a90aaa80a3377c80-1ac6-7160-e053-2a95a90a395c2020-05-18WarningsExact identifier
spl id: a5f683d3-8db1-1a28-e053-2995a90aaa80
spl set id: a3377c80-1ac6-7160-e053-2a95a90a395c

Reported adverse events (FAERS/openFDA)#

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