FDA.reportPublic FDA data

MedBox Hand Sanitizer

Manufacturer
Harper’s Pharmacy, Inc.
Effective date
2024-12-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:48:07

Label at a glance#

ProductMedBox Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin. For use when soap and water are not available.

Dosage and administration

Spray 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 Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only.

Flammable
Keep away from fire or flame

Do not use

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

When using this productkeep out of eyes,ears, and mouth. In case of contact with eyes, rinse thoroughly with water.

Stop use and ask a doctor if irritation and redness develop and last for more than 72 hours.

Keep out of reach of children.If swallowed, get medical help or contact aPoison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Spray 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

  • Do not store above 104°F (40°C)
  • May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Linalool, D-limonene, Geraniol, Citral

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047755ethanol 75 % Topical SolutionPSN2
1047755ethanol 0.75 ML/ML Topical SolutionSCD2
1047755ethanol 75 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83638-001-012024-01-30C16284748780-11030e365-3601-111a-e063-dadaa90a10e2f66c6abe-161c-48fa-8736-0abf97c3799a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83638-001-01MedBox Hand Sanitizer20 in 1 BOXLIQUID202
83638-001-01MedBox Hand Sanitizer30 mL in 1 BOTTLE, SPRAYLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83638-001MEDBOX HAND SANITIZER (ALCOHOL) LIQUID [HARPER’S PHARMACY, INC.]2Current NDC, 2 package rows20241222_f66c6abe-161c-48fa-8736-0abf97c3799a.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83638-00183638-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
LINALOOL, (+/-)-D81QY6I88EIACT
LIMONENE, (+)-GFD7C86Q1WIACT
GERANIOLL837108USYIACT
CITRALT7EU0O9VPPIACT
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
MedBox Hand SanitizerALCOHOLHarpers Pharmacy, Inc.f66c6abe-161c-48fa-8736-0abf97c3799a2024-12-20WarningsExact identifier
ndc (package): 83638-001-01
ndc (product): 83638-001
ndc11 (package): 83638000101
spl id: 29b33f35-6a7e-4ad0-e063-6394a90a61e0
spl set id: f66c6abe-161c-48fa-8736-0abf97c3799a

Reported adverse events (FAERS/openFDA)#

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