FDA.reportPublic FDA data

ezPharm Hand Sanitizing Tissue

Manufacturer
WOOIL C&TECH.CORP
Effective date
2020-07-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:21:03

Label at a glance#

ProductezPharm Hand Sanitizing Tissue
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

benzalkonium

INACTIVE INGREDIENT SECTION

Water, Glycerin, Polysorbate 80, Sodium Benzonate, Citric Acid, Maltodextrin, Aloe Barbadensis Leaf Juice Powder, Fragrance, Tocopheryl Acetate

OTC - PURPOSE SECTION

■ To decrease bacteria on the skin that could cause disease

■ Recommended for repeated use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

■ Wipe hands thoroughly with product and allow to dry.

■ Discard wipe in trash. Do not flush.

WARNINGS SECTION

■ keep out of eyes. In case of contact with eyes, flush thoroughly with water.

■ avoid contact with broken skin.

■ do not inhale or ingest.

DOSAGE & ADMINISTRATION SECTION

external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038856benzalkonium Cl 0.1 % Medicated PadPSN1
1038856benzalkonium chloride 1 MG/ML Medicated PadSCD1
1038856benzalkonium chloride 0.1 % Medicated WipesSY1
1038856benzalkonium chloride 0.1 % Topical SwabSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58474-001-012022-01-28C16284748780-1d6a99b39-aace-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58474-001-01ezPharm Hand Sanitizing Tissue80 mL in 1 PACKAGELIQUID801

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58474-001EZPHARM HAND SANITIZING TISSUE (BENZALKONIUM) LIQUID [WOOIL C&TECH.CORP]1Legacy NDC, 1 package rows20200712_a99bbfab-52e2-cc70-e053-2995a90a2372.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58474-00158474-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
SODIUM BENZOATEOJ245FE5EUIACT
MALTODEXTRIN7CVR7L4A2DIACT
ALOE VERA LEAFZY81Z83H0XIACT
POLYSORBATE 806OZP39ZG8HIACT

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
a99bb891-e6ee-f1ea-e053-2995a90abfe4a99bbfab-52e2-cc70-e053-2995a90a23722020-07-04WarningsExact identifier
spl id: a99bb891-e6ee-f1ea-e053-2995a90abfe4
spl set id: a99bbfab-52e2-cc70-e053-2995a90a2372

Reported adverse events (FAERS/openFDA)#

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