BENEMAX ADVANCED Hand Sanitizer

Manufacturer
Nugale Pharmaceutical Inc
Effective date
2021-03-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:38:58

Label at a glance#

ProductBENEMAX ADVANCED Hand Sanitizer
Active ingredientISOPROPYL ALCOHOL
Label structure9 sections

Indications and uses

Antiseptic and Hand Sanitizer to help reduce bacteria that may cause disease. For use when soap & water are unavailable.

Dosage and administration

• Place enough product on hands or affected area 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 ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 70%, USP

Purpose

OTC - PURPOSE SECTION

Antiseptic

Warnings

WARNINGS SECTION

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

Do not use
•
on 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.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Uses

INDICATIONS & USAGE SECTION

Antiseptic and Hand Sanitizer to help reduce bacteria that may cause disease. For use when soap & water are unavailable.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Inactive ingredient

INACTIVE INGREDIENT SECTION

Water

Other information

SPL UNCLASSIFIED SECTION

Store between 15 °C and 30 °C. Avoid freezing and excessive heat above 400 °C (104 °F)

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
808520isopropyl alcohol 70 % Topical SolutionPSN1
808520isopropyl alcohol 0.7 ML/ML Topical SolutionSCD1
808520isopropyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73700-004-012023-01-30C16284748780-1f386c649-ab95-0266-e053-dadaa90a7c1aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73700-004-01BENEMAX ADVANCED Hand Sanitizer473 mL in 1 BOTTLE, PLASTICLIQUID4731

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73700-004BENEMAX ADVANCED HAND SANITIZER (ISOPROPYL ALCOHOL) LIQUID [NUGALE PHARMACEUTICAL INC]1Legacy NDC, 1 package rows20210313_bcd68601-d56d-4d94-89f8-0d18be6288d7.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73700-00473700-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302ACTIB

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
bd4a0377-7e06-bd07-e053-2a95a90a339cbcd68601-d56d-4d94-89f8-0d18be6288d72021-03-11WarningsExact identifier
spl id: bd4a0377-7e06-bd07-e053-2a95a90a339c
spl set id: bcd68601-d56d-4d94-89f8-0d18be6288d7

Reported adverse events (FAERS/openFDA)#

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