Mediwiper

Manufacturer
FIRSTCHAM CO., LTD
Effective date
2020-10-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:31:09

Label at a glance#

ProductMediwiper
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Dosage and administration

■ Wet hands thoroughly with product and allow to dry without wiping ■ Do not flush

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Phenoxyethanol, Glycerin, Sodium benzoate, Polysorbate 20, Disodium EDTA, Tocopheryl acetate, Citric acid

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

■ If swallowed, get medical help or contact a Posion Control Center right away

Use

INDICATIONS & USAGE SECTION

■ Instant hand antiseptic to decrease bacteria on the skin

WARNINGS

WARNINGS SECTION

Warnings


For external use only


Stop use and ask a doctor if
■ hypersensitivity symptoms such as erythema, itching and dermatitis happen
■ skin irritation happens


Do not use
■ in combination with soap or antibacterial cleansing agents
■ the product for a long time in the same area as swelling, inflammation or sickness may occur due to absorption through the skin


When using this product
■ avoid using repeatedly in the same area, skin irritation may occur
■ avoid getting into the eyes (if contact occurs, wash well with clean water)
■ if following abnormal symptoms persist, discontinue use: Irritation around the eyes, ears, mucous membranes, including the mouth, skin irritation, and rashes

Directions

DOSAGE & ADMINISTRATION SECTION

■ Wet hands thoroughly with product and allow to dry without wiping

■ Do not flush

Other information

OTHER SAFETY INFORMATION

■ Read the directions and warnings before use ■ Avoid freezing and excessive heat above 40 ℃ (104 ℉)

Package Label - Mediwiper / 850g (200ct)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of containerImage of container

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
73923-0130-12022-07-29C16284748780-1e4f33bdf-9faa-d8a0-e053-dadaa90a6e4eDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73923-0130-1Mediwiper850 g in 1 CONTAINERLIQUID8501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73923-0130MEDIWIPER (BENZALKONIUM CHLORIDE) LIQUID [FIRSTCHAM CO., LTD]1Legacy NDC, 1 package rows20201007_e6501e52-7c3f-41c8-ae61-3a38e43f4b18.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73923-013073923-0130-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

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
a8dbd01b-5f06-4b01-b295-01d6b4560de5e6501e52-7c3f-41c8-ae61-3a38e43f4b182020-10-06WarningsExact identifier
spl id: a8dbd01b-5f06-4b01-b295-01d6b4560de5
spl set id: e6501e52-7c3f-41c8-ae61-3a38e43f4b18

Reported adverse events (FAERS/openFDA)#

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