Refreshed Traveler Foaming Hand Sanitizer

Manufacturer
Plane It Safe LLC | Nantong Health & Beyond Hygienic Products Inc.
Effective date
2020-08-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:26:17

Label at a glance#

ProductRefreshed Traveler Foaming Hand Sanitizer
Active ingredientBENZETHONIUM CHLORIDE
Label structure8 sections

Dosage and administration

Place a small amount of product inside the palm of your hand and gently rub together until dry

Label contents#

Full prescribing information#

INACTIVE INGREDIENT SECTION

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

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride

Directions

DOSAGE & ADMINISTRATION SECTION

Place a small amount of product inside the palm of your hand and gently rub together until dry

INDICATIONS & USAGE SECTION

Decreases bacteria on hands

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

For external use only. In case of contact with eyes rinse immediately with plenty of water. If rash or irritation consult a doctor. Keep out of the reach of children.

WARNINGS SECTION

For external use only. In case of contact with eyes rinse immediately with plenty of water. If rash or irritation consult a doctor. Keep out of the reach of children.

OTC - PURPOSE SECTION

Decrease the bacteria on hands

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottleLabelLabelFoaming Hand Sanitizer - Alcohol Free

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72920-2014-1Refreshed Traveler Foaming Hand Sanitizer50 mL in 1 BOTTLELIQUID502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72920-2014REFRESHED TRAVELER FOAMING HAND SANITIZER (HAND SANITIZER) LIQUID [PLANE IT SAFE LLC]2Legacy NDC, 1 package rows20200830_ab461050-1855-1c9e-e053-2a95a90a8a74.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
72920-201472920-2014-1

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
BENZETHONIUM CHLORIDEPH41D05744ACTIB
WATER059QF0KO0RIACT

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
ae0f230f-8236-73fb-e053-2a95a90a0b2bab461050-1855-1c9e-e053-2a95a90a8a742020-08-29WarningsExact identifier
spl id: ae0f230f-8236-73fb-e053-2a95a90a0b2b
spl set id: ab461050-1855-1c9e-e053-2a95a90a8a74

Reported adverse events (FAERS/openFDA)#

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