FDA.reportPublic FDA data

VirtuPure

Manufacturer
Advanced Filter Systems LLC
Effective date
2020-06-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:21:18

Label at a glance#

ProductVirtuPure
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Shake before use. Put enough product in the palm of your hands to cover them entirely, and rub hands until dry. Children under 6 should be supervised while using hand sanitizer.

Storage and handling

Store below 110° F May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

INDICATIONS & USAGE SECTION

Use Hand sanitizer to help reduce bacteria on the skin. 

Warnings

WARNINGS SECTION

Flammable keep away from fire or flame.

For external use only.

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask doctor if a rash or irritation occurs. 

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep away from children.

If swallowed, seek medical help or contact a poison control center.

Directions

DOSAGE & ADMINISTRATION SECTION

Shake before use.

Put enough product in the palm of your hands to cover them entirely, and rub hands until dry.

Children under 6 should be supervised while using hand sanitizer.

Other Information

STORAGE AND HANDLING SECTION

Store below 110° F

May discolor certain fabrics or surfaces

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Glycerine, Organic Aloe Vera

SPL UNCLASSIFIED SECTION

99.9% Sulfur Free

ELIMINATES 99.9% OF GERMS

VIRUS & BACTERIA

Hand Sanitizer

Kills 99.9% of germs on the skin

Exceeds CDC standard of 60% alcohol

Purification

Our patented purification process produces a sanitizer that is 99.9% free of pesticides, heavy metals, sulfur or acids.

No Animal Testing

Doctor Recommended

Made in U.S.A.

Manufactured and distributed by

Advanced Filter Systems, LLC,

Oak Brook, IL

advancedfiltersystems.com

patented purification process

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77787-070-042022-01-28C16284748780-1d6a99b39-76e1-a426-e053-dadaa90af4c2Virtupure™ PURIFIED hand sanitizer
77787-070-082022-01-28C16284748780-1d6a99b39-76e1-a426-e053-dadaa90af4c2Virtupure™ PURIFIED hand sanitizer
77787-070-162022-01-28C16284748780-1d6a99b39-76e1-a426-e053-dadaa90af4c2Virtupure™ PURIFIED hand sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77787-070-04VirtuPure118 mL in 1 BOTTLELIQUID1181
77787-070-08VirtuPure236.6 mL in 1 BOTTLELIQUID236.61
77787-070-16VirtuPure3785 mL in 1 BOTTLELIQUID37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77787-070VIRTUPURE (ETHYL ALCOHOL) LIQUID [ADVANCED FILTER SYSTEMS LLC]1Legacy NDC, 3 package rows20200715_86f9594c-fddd-43d3-b63b-077240ecc844.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77787-07077787-070-04, 77787-070-08, 77787-070-16

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
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT

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
631ec80a-7d9c-42ab-b544-7c5a73c70c6c86f9594c-fddd-43d3-b63b-077240ecc8442020-06-26WarningsExact identifier
spl id: 631ec80a-7d9c-42ab-b544-7c5a73c70c6c
spl set id: 86f9594c-fddd-43d3-b63b-077240ecc844

Reported adverse events (FAERS/openFDA)#

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