FDA.reportPublic FDA data

Foaming 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#

ProductFoaming Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

Dispense a palm-sized amount onto hands·Rub hands together until dry

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Decreases bacteria on hands.

Warnings

WARNINGS SECTION

Use only directed. For external use only.
When using this product avoid contact with eyes.
lf contact occurs, rinse thoroughly with water.
Stop use and ask doctor if irritation and redness develop or increase.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children, except under adult supervision.
If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Dispense a palm-sized amount onto hands·Rub hands together until dry

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua),PEG-40 Hydrogenated Castor Oil, Glycerin, Fragrance
(ParfumDidecyldimonium Chloride, Phenoxy-
ethanol, Polyaminopropyl Biguanide, Citric Acid,
Citrus Limon (lemon)Peel Oil, Yellow 5(Cl19140), Red 4 (CI 14700)

Eucalyptus Globulus Leaf Oil,Blue 1(CI 42090)

Vanilla Planifolia Fruit Oil,Red 33(CI 172000)

Mangifera Indica(mango)Seed Oil

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11223344

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51706-940-012022-03-21C16284748780-1d6a99b39-9405-a426-e053-dadaa90af4c251706-940 Foaming Hand Sanitizer 0.1% Benzalkonium chloride
51706-940-012022-01-28C16284748780-1d6a99b39-9405-a426-e053-dadaa90af4c251706-940 Foaming Hand Sanitizer 0.1% Benzalkonium chloride

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51706-94051706-940-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
POLYAMINOPROPYL BIGUANIDEDT9D8Z79ETIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
EUCALYPTUS OIL2R04ONI662IACT
FD&C RED NO. 4X3W0AM1JLXIACT
MANGO SEED OILK8LOR30915IACT
VANILLA PLANIFOLIA OIL0A3F415158IACT
PHENOXYETHANOLHIE492ZZ3TIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
LEMON OILI9GRO824LLIACT
D&C RED NO. 339DBA0SBB0LIACT

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
23ccaaa4-b497-d142-e063-6394a90a1d4aada9d426-0e56-203e-e053-2a95a90a8dfc2024-10-06WarningsExact identifier
spl set id: ada9d426-0e56-203e-e053-2a95a90a8dfc

Reported adverse events (FAERS/openFDA)#

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