FDA.reportPublic FDA data

VINIFERAMINE HAND SANITIZER

Manufacturer
MCCORD RESEARCH | Wasatch Product Development, LLC
Effective date
2022-01-25
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 23:47:37

Label at a glance#

ProductVINIFERAMINE HAND SANITIZER
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

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

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

Label contents#

Full prescribing information#

Active lngredient  

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol

Purpose 

OTC - PURPOSE SECTION

Antiseptic 

Uses 

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

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

SPL UNCLASSIFIED SECTION

Store between 15-30°C (59-86F)

Avoid freezing and excessive heat above 40°C (104F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Pyrus Malus (Apple) Fruit Extract, Fragrance

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1944524ethanol 64 % Topical SprayPSN5
1944524ethanol 0.64 ML/ML Topical SpraySCD5
1944524ethanol 64 % Topical SpraySY5

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71358-017-022024-01-30C16284748780-11030e365-40cf-111a-e063-dadaa90a10e2VINIFERAMINE HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71358-017-02VINIFERAMINE HAND SANITIZER237 mL in 1 BOTTLESPRAY2375

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71358-017VINIFERAMINE HAND SANITIZER (ETHYL ALCOHOL) SPRAY [MCCORD RESEARCH]5Legacy NDC, 1 package rows20220126_c7046232-342f-4e4a-b172-48c306c3fc28.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
71358-01771358-017-02

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
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
APPLEB423VGH5S9IACT
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
d66df19e-04b6-a5c7-e053-2a95a90a7ca7c7046232-342f-4e4a-b172-48c306c3fc282022-01-25WarningsExact identifier
spl id: d66df19e-04b6-a5c7-e053-2a95a90a7ca7
spl set id: c7046232-342f-4e4a-b172-48c306c3fc28

Reported adverse events (FAERS/openFDA)#

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