Label at a glance#

ProductFreshorize hand sanitizer

Active ingredientAlcohol

Label structure7 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

62.5% Ethyl Alcohol.

Use Information

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

Safety: For External Use Only.Use on Hands only.

Flammable. Keep away from fire or flame.

Avoid contact with Eyes, should this occur rinse immediately with clean warm water.

Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Display of package label.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Picture of Package Label

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Purpose

OTC - PURPOSE SECTION

Kills 99.9% Bacteria

DOSAGE & ADMINISTRATION SECTION

Requires no water or towels.

Apply small amount to hands and rub lightly until dry.

INACTIVE INGREDIENT SECTION

Alcohol denat, Aqua, acrylates/C10-30 alkyl, acrylate cross polymer, triethanolamine (TEA), parfum

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1039474	ethanol 62.5 % Topical Solution	PSN	1
1039474	ethanol 0.625 ML/ML Topical Solution	SCD	1
1039474	ethanol 62.5 % Topical Solution	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
52305-200-20	2019-10-29	C162847	48780-1	960f7f55-d370-8e05-e053-dbdaa90a074a	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
52305-200-20	Freshorizehand sanitizer	295 mL in 1 BOTTLE, PUMP	LOTION	295		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52305-200	FRESHORIZE HAND SANITIZER (ALCOHOL) LOTION [FRESHORIZE, LTD.]	1	Legacy NDC, 1 package rows	20101130_5ae9abff-f21a-447e-bc97-2dafcdf405f4.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Alcohol	ACTIVE INGREDIENT	3K9958V90M	1
alcohol	ACTIVE MOIETY	3K9958V90M	1
ETHANOLAMINE	INACTIVE INGREDIENT	5KV86114PT	1
Water	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Freshorize hand sanitizer
Alcohol
Water
ETHANOLAMINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
52305-200	52305-200-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Alcohol	3K9958V90M	ACTIB
Water	059QF0KO0R	IACT
ETHANOLAMINE	5KV86114PT	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 1 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
ETHANOLAMINE	2-AMINOETHANOL	5KV86114PT	TABLET, DELAYED RELEASE / ORAL		1 mg	Exact identifier — unii candidate

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
99c19d09-7127-414c-891d-e864c840a1a7			5ae9abff-f21a-447e-bc97-2dafcdf405f4	2010-11-20	Warnings	Exact identifier spl id: 99c19d09-7127-414c-891d-e864c840a1a7 spl set id: 5ae9abff-f21a-447e-bc97-2dafcdf405f4

Reported adverse events (FAERS/openFDA)#

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