FDA.reportPublic FDA data

MEDISIDE-HAND ANTISEPTIC TISSUE

Manufacturer
YOU HAN GREENTECH
Effective date
2022-07-05
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:50:04

Label at a glance#

ProductMEDISIDE-HAND ANTISEPTIC TISSUE
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE 0.1%

PURPOSE

OTC - PURPOSE SECTION

ANTIMICROBIAL

Direction

DOSAGE & ADMINISTRATION SECTION

To dispense, peel back front label at tab

Remove towelettes as needed

Reseal pouch by pressing label firmly back into place

Do not use

OTC - DO NOT USE SECTION

do not flush

do not use if you are allergic to any of the ingredients

Warnings

WARNINGS SECTION

for external sue only.

sotre away from direct sunlight or high temperature.

use caution near electric appliances to avoid electric shock.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

stop use and ask a doctor.

OTC - STOP USE SECTION

stop use and ask a doctor if irritationor or rash edvelopes and continues for more than 72 hours.

Use

INDICATIONS & USAGE SECTION

peel back front label slowy.

use caution near electric appliances to avoid electric shock

ask a doctor

OTC - ASK DOCTOR SECTION

f swallowed, get medical help or contact a Poison control center right away

Other information

OTHER SAFETY INFORMATION

7.9 in x 5.9 in (20cm x15cm )

INACTIVE INGREDIEINT

INACTIVE INGREDIENT SECTION

Aqua

Glycerine

Orange Sweet Ext.

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

79893-402-0179893-402-01

79893-402-0279893-402-02

79893-402-0379893-402-03

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038856benzalkonium Cl 0.1 % Medicated PadPSN4
1038856benzalkonium chloride 1 MG/ML Medicated PadSCD4
1038856benzalkonium chloride 0.1 % Medicated WipesSY4
1038856benzalkonium chloride 0.1 % Topical SwabSY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78583-701-012024-01-30C16284748780-11030e365-127f-111a-e063-dadaa90a10e278583-701
78583-701-022024-01-30C16284748780-11030e365-127f-111a-e063-dadaa90a10e278583-701
78583-701-032024-01-30C16284748780-11030e365-127f-111a-e063-dadaa90a10e278583-701

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78583-701-01MEDISIDE-HAND ANTISEPTIC TISSUE66 g in 1 POUCHLIQUID664
78583-701-02MEDISIDE-HAND ANTISEPTIC TISSUE132 g in 1 POUCHLIQUID1324
78583-701-03MEDISIDE-HAND ANTISEPTIC TISSUE198 g in 1 POUCHLIQUID1984

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78583-701MEDISIDE-HAND ANTISEPTIC TISSUE (BENZALKONIUM CHLORIDE) LIQUID [YOU HAN GREENTECH]4Legacy NDC, 3 package rows20220706_e309c797-8009-82ae-e053-2a95a90a4ffd.zip

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
78583-70178583-701-01, 78583-701-02, 78583-701-03

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
GLYCERINPDC6A3C0OXIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
ORANGE OILAKN3KSD11BIACT
WATER059QF0KO0RIACT

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
e308af8e-65fa-f986-e053-2995a90a74d2e309c797-8009-82ae-e053-2a95a90a4ffd2022-07-05WarningsExact identifier
spl id: e308af8e-65fa-f986-e053-2995a90a74d2
spl set id: e309c797-8009-82ae-e053-2a95a90a4ffd

Reported adverse events (FAERS/openFDA)#

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