FDA.reportPublic FDA data

Freshorize

Manufacturer
Freshorize, Ltd.
Effective date
2010-11-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:26:31

Label at a glance#

ProductFreshorize Alcohol Free foaming hand sanitizer
Active ingredientBenzalkonium Chloride
Label structure7 sections

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

0.13% Benzylkonium Chloride

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION


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

Caution: Use on hands only.



 

Display of package label.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Picture of Package Label

freshorize Non-Alc label
freshorize Non-Alc 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

Aqua, Polysorbate 40, Aloe Barbadensis, Parfum

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020365benzalkonium chloride 0.13 % Topical FoamPSN1
1020365benzalkonium chloride 1.3 MG/ML Topical FoamSCD1
1020365benzalkonium chloride 0.13 % Topical FoamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52305-300-202019-10-29C16284748780-1960f7f55-db9b-8e05-e053-dbdaa90a074aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52305-300-20FreshorizeAlcohol Free foaming hand sanitizer280 mL in 1 BOTTLE, PUMPLOTION2801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52305-300FRESHORIZE ALCOHOL FREE FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) LOTION [FRESHORIZE, LTD.]1Legacy NDC, 1 package rows20101206_94ccfa10-ce10-41f2-a423-a19738145bd7.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Benzalkonium ChlorideACTIVE INGREDIENTF5UM2KM3W71
BenzalkoniumACTIVE MOIETY7N6JUD5X6Y1
ALOE VERA FLOWERINACTIVE INGREDIENT575DY8C1ER1
POLYSORBATE 40INACTIVE INGREDIENTSTI11B5A2X1
WaterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52305-30052305-300-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
Benzalkonium ChlorideF5UM2KM3W7ACTIB
Water059QF0KO0RIACT
POLYSORBATE 40STI11B5A2XIACT
ALOE VERA FLOWER575DY8C1ERIACT

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 · 7 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
POLYSORBATE 40POLYSORBATE 40STI11B5A2XLIQUID / TOPICAL2 %w/wExact identifier — unii candidate
7 equally ranked IID candidates
POLYSORBATE 40POLYSORBATE 40STI11B5A2XDROPS / ORAL0.02 mlExact identifier — unii candidate
7 equally ranked IID candidates
POLYSORBATE 40POLYSORBATE 40STI11B5A2XGEL / TOPICAL28 mgExact identifier — unii candidate
7 equally ranked IID candidates
POLYSORBATE 40POLYSORBATE 40STI11B5A2XLOTION / TOPICAL40 mgExact identifier — unii candidate
7 equally ranked IID candidates
POLYSORBATE 40POLYSORBATE 40STI11B5A2XELIXIR / ORAL0.05 mg/5mlExact identifier — unii candidate
7 equally ranked IID candidates
POLYSORBATE 40POLYSORBATE 40STI11B5A2XSUSPENSION / ORALNAExact identifier — unii candidate
7 equally ranked IID candidates
POLYSORBATE 40POLYSORBATE 40STI11B5A2XCREAM / TOPICAL3 %w/wExact identifier — unii candidate
7 equally ranked IID candidates

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
26655249-257e-4763-bee6-1dcddb69292594ccfa10-ce10-41f2-a423-a19738145bd72010-11-20WarningsExact identifier
spl id: 26655249-257e-4763-bee6-1dcddb692925
spl set id: 94ccfa10-ce10-41f2-a423-a19738145bd7

Reported adverse events (FAERS/openFDA)#

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