FDA.reportPublic FDA data

Quantum Medium Viscosity Gel Hand Sanitizer

Manufacturer
Quantum Valve And Oilfield Solutions, Llc
Effective date
2020-09-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:28:59

Label at a glance#

ProductQuantum Medium Viscosity Gel Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Storage and handling

OTHER INFORMATION Store between 15°-30°C (59° - 86°F) Avoid freezing and excessive heat above 40°C (104°F) 

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Alcohol 72% v/v

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

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:
· On children less than two 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 maybe 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.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using to avoid swallowing.

STORAGE AND HANDLING SECTION

OTHER INFORMATION Store between 15°-30°C (59° - 86°F)
Avoid freezing and excessive heat above 40°C (104°F) 

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS ethyl acrylate copolymer*, ethyl methacrylate*, fragrance (parfum), glycerin, purified water USP, triethanolamine

*Contains one of more of these ingredients

SPL UNCLASSIFIED SECTION

MADE IN THE USA · DUNS (10-906-5471) 

TOPICAL ANTISEPTIC GEL HAND SANITIZER
KILLS 99.9% OF ILLNESS CAUSING GERMS

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2277550ethanol 72 % Topical GelPSN1
2277550ethanol 0.72 ML/ML Topical GelSCD1
2277550ethanol 72 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79413-206-022022-01-28C16284748780-1d6a99b39-af8a-a426-e053-dadaa90af4c2Q UANTUM HAND SANITIZER MEDIUM VISCOSITY
79413-206-042022-01-28C16284748780-1d6a99b39-af8a-a426-e053-dadaa90af4c2Q UANTUM HAND SANITIZER MEDIUM VISCOSITY
79413-206-082022-01-28C16284748780-1d6a99b39-af8a-a426-e053-dadaa90af4c2Q UANTUM HAND SANITIZER MEDIUM VISCOSITY
79413-206-162022-01-28C16284748780-1d6a99b39-af8a-a426-e053-dadaa90af4c2Q UANTUM HAND SANITIZER MEDIUM VISCOSITY
79413-206-322022-01-28C16284748780-1d6a99b39-af8a-a426-e053-dadaa90af4c2Q UANTUM HAND SANITIZER MEDIUM VISCOSITY
79413-206-882022-01-28C16284748780-1d6a99b39-af8a-a426-e053-dadaa90af4c2Q UANTUM HAND SANITIZER MEDIUM VISCOSITY

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79413-206-02Quantum Medium Viscosity Gel Hand Sanitizer59 mL in 1 BOTTLEGEL591
79413-206-04Quantum Medium Viscosity Gel Hand Sanitizer118 mL in 1 BOTTLEGEL1181
79413-206-08Quantum Medium Viscosity Gel Hand Sanitizer237 mL in 1 BOTTLEGEL2371
79413-206-16Quantum Medium Viscosity Gel Hand Sanitizer473 mL in 1 BOTTLEGEL4731
79413-206-32Quantum Medium Viscosity Gel Hand Sanitizer946 mL in 1 BOTTLEGEL9461
79413-206-88Quantum Medium Viscosity Gel Hand Sanitizer3785 mL in 1 BOTTLEGEL37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79413-206QUANTUM MEDIUM VISCOSITY GEL HAND SANITIZER (ALCOHOL) GEL [QUANTUM VALVE AND OILFIELD SOLUTIONS, LLC]1Legacy NDC, 6 package rows20200911_234e8720-6f3e-4eb5-a76f-cc41e5c7e716.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
79413-20679413-206-02, 79413-206-04, 79413-206-08, 79413-206-16, 79413-206-32, 79413-206-88

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
ETHYL ACRYLATE71E6178C9TIACT
ETHYL METHACRYLATE80F70CLT4OIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
TROLAMINE9O3K93S3TKIACT

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
47d4c7bd-805e-41ab-8c9c-ac48dde8d988234e8720-6f3e-4eb5-a76f-cc41e5c7e7162020-09-04WarningsExact identifier
spl id: 47d4c7bd-805e-41ab-8c9c-ac48dde8d988
spl set id: 234e8720-6f3e-4eb5-a76f-cc41e5c7e716

Reported adverse events (FAERS/openFDA)#

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