Hand Sanitizer

Manufacturer
Landy International
Effective date
2022-03-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:05:30

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Place enough product in your palm to thoroughly cover your hands and rub hands together until dry.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol (Vol.%)75%

Purpose

OTC - PURPOSE SECTION

Antiseptic/Hand & Skin Sanitizer

Use

INDICATIONS & USAGE SECTION

Help decrease bacteria on the skin.
Recommended for repeated use.

Warnings

WARNINGS SECTION

Flammable. Keep away from flame and heat.

For external use only.

Avoid contact with eyes.If occurs, rinse with water.

Do not swallow. If occurs, get medical help.

Store between 32 °F-109 °F. Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product in your palm to thoroughly cover your hands and rub
hands together until dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water(Aqua), Acrylates/C10-30 alkyI acrylate crosspolymer, Glycerin,
Triethanolamine, Tocopheryl acetate, Aloe barbadensis leaf extract,
Phenoxyethanol, Ethylhexylglycerin.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51706-909-012022-03-21C16284748780-1d6a99b39-dce0-a426-e053-dadaa90af4c251706-909 Hand Sanitizer Ethyl Alcohol(75%)
51706-909-012022-01-28C16284748780-1d6a99b39-dce0-a426-e053-dadaa90af4c251706-909 Hand Sanitizer Ethyl Alcohol(75%)

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51706-90951706-909-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
23ccb954-9be7-810c-e063-6394a90a5125a92f2daa-77c8-e9a8-e053-2995a90a6dce2024-10-06WarningsExact identifier
spl set id: a92f2daa-77c8-e9a8-e053-2995a90a6dce

Reported adverse events (FAERS/openFDA)#

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