Foaming Hand Sanitizer

Manufacturer
Plane It Safe LLC
Effective date
2021-12-24
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:45:55

Label at a glance#

ProductFoaming Hand Sanitizer
Active ingredientBENZETHONIUM CHLORIDE
Label structure8 sections

Indications and uses

Decrease bacteria on hands

Dosage and administration

Directions: Place a small amount of product in your hand and rub hands together until dry.

Label contents#

Full prescribing information#

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water,Betaine,PEG-40 Hydrogenated Castor Oil, Phenoxyethanol, Diazolidinyl Urea, Palmitamidopropyltrimonium Chloride, Propylene Glycol, Fragrance, Sodium Citrate, Disodim EDTA.

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Benzethonium Chloride (0.1%)

Directions:

DOSAGE & ADMINISTRATION SECTION

Directions: Place a small amount of product in your hand and rub hands together until dry.

Uses:

INDICATIONS & USAGE SECTION

Decrease bacteria on hands

Keep out of the reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children

Warning:

WARNINGS SECTION

For external use only. In case of contact with eyes,rinse immediately with plenty of water. Discontinue use if rash or irritation occurs and consult a doctor. Keep it out of children.

Purpose

OTC - PURPOSE SECTION

Decrease Bacteria on hand

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hand SanitizerHand Sanitizer

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72920-2002-12023-01-30C16284748780-1f386c64a-11eb-0266-e053-dadaa90a7c1aFoaming Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72920-2002-1Foaming Hand Sanitizer50 mL in 1 BOTTLEGEL503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72920-2002FOAMING HAND SANITIZER (HAND SANITIZER) GEL [PLANE IT SAFE LLC]3Legacy NDC, 1 package rows20211225_9574b582-16fa-1eb1-e053-2995a90adbff.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72920-200272920-2002-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BENZETHONIUM CHLORIDEPH41D05744ACTIB

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
d3f0ad58-8b5b-925a-e053-2a95a90afa5d9574b582-16fa-1eb1-e053-2995a90adbff2021-12-24WarningsExact identifier
spl id: d3f0ad58-8b5b-925a-e053-2a95a90afa5d
spl set id: 9574b582-16fa-1eb1-e053-2995a90adbff

Reported adverse events (FAERS/openFDA)#

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