Freshorize

Manufacturer
Freshorize, Ltd.
Effective date
2010-11-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:26:49

Label at a glance#

ProductFreshorize hand sanitizer
Active ingredientAlcohol
Label structure8 sections

Label contents#

Full prescribing information#

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

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

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


Image of DisplayImage of Display

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039474ethanol 62.5 % Topical SolutionPSN2
1039474ethanol 0.625 ML/ML Topical SolutionSCD2
1039474ethanol 62.5 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52305-200-502019-10-29C16284748780-1960f7f55-c470-8e05-e053-dbdaa90a074aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52305-200-50Freshorizehand sanitizer295 mL in 1 BOTTLE, PUMPLOTION2952

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52305-200FRESHORIZE HAND SANITIZER (ALCOHOL) LOTION [FRESHORIZE, LTD.]2Legacy NDC, 1 package rows20110105_fa98974b-f439-4bf9-a673-ea42633da3be.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AlcoholACTIVE INGREDIENT3K9958V90M2
alcoholACTIVE MOIETY3K9958V90M2
ETHANOLAMINEINACTIVE INGREDIENT5KV86114PT2
WaterINACTIVE INGREDIENT059QF0KO0R2

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52305-20052305-200-50

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
NameUNIIKind
Alcohol3K9958V90MACTIB
Water059QF0KO0RIACT
ETHANOLAMINE5KV86114PTIACT

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 ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ETHANOLAMINE2-AMINOETHANOL5KV86114PTTABLET, DELAYED RELEASE / ORAL1 mgExact 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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
9ccaf1be-aacf-4d1b-a10d-a87498dfdf0dfa98974b-f439-4bf9-a673-ea42633da3be2010-11-20WarningsExact identifier
spl id: 9ccaf1be-aacf-4d1b-a10d-a87498dfdf0d
spl set id: fa98974b-f439-4bf9-a673-ea42633da3be

Reported adverse events (FAERS/openFDA)#

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