Hand Sanitizer with Aloe Vera

Manufacturer
Kentron Healthcare, Inc.
Effective date
2016-02-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:45:01

Label at a glance#

ProductHand Sanitizer with Aloe Vera
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient
Ethyl Alcohol 62%

OTC - PURPOSE SECTION

Purpose

Antiseptic

WARNINGS SECTION

Warning

For external use only

Flammable

Keep away from fire or flame

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 immediately

DOSAGE & ADMINISTRATION SECTION

Directions

Squeeze on hands and rub hands together until dry

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Water, Aloe Barbadensis Leaf Juice, Glycerin, Propylene Glycol, Carbomer, Aminomethyl Propanol, Fragrance

INDICATIONS & USAGE SECTION

Use

Decreases bacteria on the hands

OTHER SAFETY INFORMATION

Keep out of eyes

In case of eye contact immediately flush with water and get medical help

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of bottle labelimage of bottle label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN1
581660ethanol 0.62 ML/ML Topical GelSCD1
581660ethanol 62 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69556-001-012023-01-30C16284748780-1f386c649-d66d-0266-e053-dadaa90a7c1a2bf11a5d-fa89-6a1e-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69556-001-01Hand Sanitizer with Aloe Vera236 mL in 1 BOTTLE, PLASTICGEL2361

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69556-001HAND SANITIZER WITH ALOE VERA (ETHYL ALCOHOL) GEL [KENTRON HEALTHCARE, INC.]1Legacy NDC, 1 package rows20160217_2bf11a5d-fa89-6a1e-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69556-00169556-001-01

Ingredients#

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

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

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
2bf11a5d-fa88-6a1e-e054-00144ff88e882bf11a5d-fa89-6a1e-e054-00144ff88e882016-02-17WarningsExact identifier
spl id: 2bf11a5d-fa88-6a1e-e054-00144ff88e88
spl set id: 2bf11a5d-fa89-6a1e-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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