FDA.reportPublic FDA data

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 22:05:31

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

EthyI Alcohol (Vol.%)65%

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help decrease bacteria on the skin
Recommended for repeated use.

Warnings

WARNINGS SECTION

Flammable. Keep away from flame and heat.
For external use only.Do not swallow.
Avoid contact with eyes. If contact occurs, rinse with water.
Keep out of reach of children.Store between 32 °F-109 °F

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
51706-941-012022-03-21C16284748780-1d6a99b39-c86c-a426-e053-dadaa90af4c251706-941 hand sanitizer 65% alcohol
51706-941-012022-01-28C16284748780-1d6a99b39-c86c-a426-e053-dadaa90af4c251706-941 hand sanitizer 65% alcohol

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51706-94151706-941-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
PHENOXYETHANOLHIE492ZZ3TIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
ETHYLHEXYLGLYCERIN147D247K3PIACT
TROLAMINE9O3K93S3TKIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE VERA LEAFZY81Z83H0XIACT

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
23cc4574-deb9-4af9-e063-6294a90acb4eadaa8767-31c3-1e98-e053-2a95a90a7b932024-10-06WarningsExact identifier
spl set id: adaa8767-31c3-1e98-e053-2a95a90a7b93

Reported adverse events (FAERS/openFDA)#

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