Antibacterial Hand Sanitizer

Manufacturer
Prostock LLC.
Effective date
2023-12-12
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:04:15

Label at a glance#

ProductAntibacterial Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

•For Hand Sanitizing

Dosage and administration

•Wet hands thoroughly with product and allow to dry without wiping. •For children under 6 age use only under adult supervision. •Not recommended for infants.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

•For Hand Sanitizing

Warnings

WARNINGS SECTION

For external use only-hands.
Flammable. Keep away from heat and flame.

When using this product

OTC - WHEN USING SECTION

Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.

Stop use and ask a doctor if

OTC - STOP USE SECTION

skin irritation develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or call a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

•Wet hands thoroughly with product and allow to dry without wiping.

•For children under 6 age use only under adult supervision.
•Not recommended for infants.

Other Information

SPL UNCLASSIFIED SECTION

•Do not store above 105°F.
•May discolor some fabrics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Carborner, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine, Water.

Package Labeling: 73796-110-15

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling: 73796-110-30

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Package Labeling: 73796-110-60

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN2
581660ethanol 0.62 ML/ML Topical GelSCD2
581660ethanol 62 % Topical GelSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73796-110-15Antibacterial Hand Sanitizer15 mL in 1 BOTTLEGEL152
73796-110-30Antibacterial Hand Sanitizer30 mL in 1 BOTTLEGEL302
73796-110-60Antibacterial Hand Sanitizer60 mL in 1 BOTTLEGEL602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73796-110ANTIBACTERIAL HAND SANITIZER (ALCOHOL) GEL [PROSTOCK LLC.]2Current NDC, Legacy NDC, 3 package rows20231214_a184c473-6fa8-f09b-e053-2a95a90a1b17.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
73796-11073796-110-15, 73796-110-30, 73796-110-60

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Antibacterial Hand SanitizerALCOHOLProstock LLC.a184c473-6fa8-f09b-e053-2a95a90a1b172023-12-12WarningsExact identifier
ndc (package): 73796-110-30
ndc (package): 73796-110-15
ndc (package): 73796-110-60
ndc (product): 73796-110
ndc11 (package): 73796011060
ndc11 (package): 73796011015
ndc11 (package): 73796011030
spl id: 0c53824b-1b8d-a3f8-e063-6394a90aacb7
spl set id: a184c473-6fa8-f09b-e053-2a95a90a1b17
Antibacterial Hand SanitizerALCOHOLProstock LLC1f4833c5-fcac-4c01-a5c6-e72837ca0a482023-11-06WarningsExact identifier
ndc (product): 73796-110

Reported adverse events (FAERS/openFDA)#

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