Refreshed Traveler Hand Sanitizer with Aloe

Manufacturer
Plane It Safe LLC
Effective date
2020-06-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:24:48

Label at a glance#

ProductRefreshed Traveler Hand Sanitizer with Aloe
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Hand Sanitizer to decrease bacteria on the skin

Dosage and administration

Thoroughly apply product on hands & rub together until dry. Adult supervision recommended for anyone 6 years of age & under.

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Ethanol 70%

Purpose:

OTC - PURPOSE SECTION

Antiseptic

Uses:

INDICATIONS & USAGE SECTION

Hand Sanitizer to decrease bacteria on the skin

WARNINGS:

WARNINGS SECTION

FOR EXTERNAL USE ONLY.

Flammable. Keep away from fire and flame.

When using this product

OTC - WHEN USING SECTION

do NOT use in or around the eye.

In case of contact, flush eyes with water thoroughly.

Keep out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Do not ingest - If swallowed get medical help or contact a poison control center immediately.

Stop use and contact a physician if

OTC - STOP USE SECTION

irritation, redness or rash develops and persist for longer than 72 hours.

Directions:

DOSAGE & ADMINISTRATION SECTION

Thoroughly apply product on hands & rub together until dry. Adult supervision recommended for anyone 6 years of age & under.

Other information:

SPL UNCLASSIFIED SECTION

Do not store above 105F. May discolor some fabrics and finishes. Harmful to wood finishes and plastics.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Aqua (Water), Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Extract, Triethanolaine, Parfum (Fragrance)

Questions or comments?

OTC - QUESTIONS SECTION

1-888-840-0499

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72920-000272920-0002-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
d4aed8f9-44a3-3d5f-e053-2a95a90a2922a8aed95e-05ba-e4c7-e053-2a95a90a4a362022-01-03WarningsExact identifier
spl set id: a8aed95e-05ba-e4c7-e053-2a95a90a4a36

Reported adverse events (FAERS/openFDA)#

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