United Airlines Gel Hand Sanitizer.DCR

Manufacturer: Freshorize Ltd. | Freshorize LLC
Effective date: 2020-07-08
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:20:38

Label at a glance#

ProductUnited Airlines

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

To decrease bacteria on the skin that could cause disease. Recommended for repeated use.

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.

Label contents#

Full prescribing information#

Uses:

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that could cause disease. Recommended for repeated use.

Warnings:

WARNINGS SECTION

Flammable - Keep away from fire or flame
For external use only.
When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water.
Avoid contact with broken skin.
Do not inhale or ingest
Stop use and ask doctor is rash or irritation develops and lasts more than 72 hours.
If product is swallowed, get medical help or contact a Poison Control Center right away.

Warnings:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

Directions:

INSTRUCTIONS FOR USE SECTION

Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision.

Not recommended for infants.

Other information:

OTHER SAFETY INFORMATION

Do not store above 105°
May discolor some fabrics
Harmful to wood finish and plastics.

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient: Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Water, Isopropyl Alcohol, Tocopheryl Acetate, Glycerin, Propylene Glycol, Isopropyl Myristate, Carbomer, Aminomethyl Propanol

Brand Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2.5oz Label

Front Label

DOSAGE & ADMINISTRATION SECTION

Requires no water or towels.
Apply small amount to hands and rub lightly until dry.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
52305-223-01	2023-01-30	C162847	48780-1	f386c649-bbd1-0266-e053-dadaa90a7c1a	United Airlines Gel Hand Sanitizer.DCR
52305-223-02	2023-01-30	C162847	48780-1	f386c649-bbd1-0266-e053-dadaa90a7c1a	United Airlines Gel Hand Sanitizer.DCR

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
52305-223-01	United Airlines	60 mL in 1 BOTTLE, PUMP	GEL	60		2
52305-223-02	United Airlines	236 mL in 1 BOTTLE, PUMP	GEL	236		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52305-223	UNITED AIRLINES (ALCOHOL) GEL [FRESHORIZE LTD.]	2	Legacy NDC, 2 package rows	20200709_a9cae925-1d22-4a63-e053-2a95a90ae234.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

United Airlines
Alcohol
ISOPROPYL MYRISTATE
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
GLYCERIN
PROPYLENE GLYCOL
ISOPROPYL ALCOHOL
.ALPHA.-TOCOPHEROL ACETATE
AMINOMETHYLPROPANOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
52305-223	52305-223-01, 52305-223-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
GLYCERIN	PDC6A3C0OX	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
ISOPROPYL ALCOHOL	ND2M416302	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a9ee1c60-608b-2229-e053-2995a90aa528			a9cae925-1d22-4a63-e053-2a95a90ae234	2020-07-08	Warnings	Exact identifier spl id: a9ee1c60-608b-2229-e053-2995a90aa528 spl set id: a9cae925-1d22-4a63-e053-2a95a90ae234

Reported adverse events (FAERS/openFDA)#

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