FDA.reportPublic FDA data

Hand sanitizer

Manufacturer
Landy International
Effective date
2019-11-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:02:19

Label at a glance#

ProductHand sanitizer
Active ingredientALCOHOL
Label structure13 sections

Label contents#

Full prescribing information#

INACTIVE INGREDIENT SECTION

inactive ingredientinactive ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol Denat. 62%

DOSAGE & ADMINISTRATION SECTION

dosagedosage

WARNINGS SECTION

warningwarning

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep outkeep out

INDICATIONS & USAGE SECTION

indicationindication

OTC - PURPOSE SECTION

purposepurpose

701

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

701 package701 package

702

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

702 package702 package

703

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

703 package703 package

704

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

704 package704 package

705

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

705 package705 package

706

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

706 package706 package

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51706-707-012024-06-13C16284748780-1ba0f9c33-29dd-a910-e053-dadaa90a0b856c5f1846-6b66-0136-e053-2991aa0a4b1d
51706-708-012024-06-13C16284748780-1ba0f9c33-29dd-a910-e053-dadaa90a0b856c5f1846-6b66-0136-e053-2991aa0a4b1d
51706-709-012024-06-13C16284748780-1ba0f9c33-29dd-a910-e053-dadaa90a0b856c5f1846-6b66-0136-e053-2991aa0a4b1d
51706-710-012024-06-13C16284748780-1ba0f9c33-29dd-a910-e053-dadaa90a0b856c5f1846-6b66-0136-e053-2991aa0a4b1d
51706-711-012024-06-13C16284748780-1ba0f9c33-29dd-a910-e053-dadaa90a0b856c5f1846-6b66-0136-e053-2991aa0a4b1d
51706-712-012024-06-13C16284748780-1ba0f9c33-29dd-a910-e053-dadaa90a0b856c5f1846-6b66-0136-e053-2991aa0a4b1d
51706-707-012021-01-29C16284748780-1ba0f9c33-29dd-a910-e053-dadaa90a0b856c5f1846-6b66-0136-e053-2991aa0a4b1d
51706-708-012021-01-29C16284748780-1ba0f9c33-29dd-a910-e053-dadaa90a0b856c5f1846-6b66-0136-e053-2991aa0a4b1d
51706-709-012021-01-29C16284748780-1ba0f9c33-29dd-a910-e053-dadaa90a0b856c5f1846-6b66-0136-e053-2991aa0a4b1d
51706-710-012021-01-29C16284748780-1ba0f9c33-29dd-a910-e053-dadaa90a0b856c5f1846-6b66-0136-e053-2991aa0a4b1d
51706-711-012021-01-29C16284748780-1ba0f9c33-29dd-a910-e053-dadaa90a0b856c5f1846-6b66-0136-e053-2991aa0a4b1d
51706-712-012021-01-29C16284748780-1ba0f9c33-29dd-a910-e053-dadaa90a0b856c5f1846-6b66-0136-e053-2991aa0a4b1d

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51706-70751706-707-01
51706-70851706-708-01
51706-70951706-709-01
51706-71051706-710-01
51706-71151706-711-01
51706-71251706-712-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML · Source PDF

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
1ac16b0b-3566-987e-e063-6294a90ab6b26c5f1846-6b66-0136-e053-2991aa0a4b1d2024-06-13WarningsExact identifier
spl set id: 6c5f1846-6b66-0136-e053-2991aa0a4b1d

Reported adverse events (FAERS/openFDA)#

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