MediClean Sanitizing

Manufacturer
Industrias Maquín, S.A. de C.V.
Effective date
2023-11-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:20:55

Label at a glance#

ProductMediClean Sanitizing
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

Wet hands thoroughly with product and allow to dry.

Label contents#

Full prescribing information#

Activate ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only:

When using this product.

OTC - WHEN USING SECTION

Do not use in or near the eyes, in case of contact, rinse eyes throughly with water.

Stop using and ask a doctor if:

OTC - STOP USE SECTION

Irritation or rash appears and lasts.

Keep out of reach of children:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get medical help or contact a poison control center rigth away.

Children under 6 years of age should be supervised when using MEDICLEAN.

Directions:

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Aqua, Laurylamine Dipropylenediamine, Dipropylene Glycol, Phenoxyethanol, Fragrance, PEG 40 Hydrogenated Castor Oil, Glycerin, Sodium Cocoamphoacetate, Isopropyl Alcohol, Citric Acid, Tetrasodium EDTA, Laureth-7 Citrate.

Package Labeling:48ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Package Labeling:16ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79432-000MEDICLEAN SANITIZING (BENZALKONIUM CHLORIDE) CLOTH [INDUSTRIAS MAQUÍN, S.A. DE C.V.]2Legacy NDC20231115_aaf83399-9eb5-4ea7-e053-2a95a90a7322.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79432-00079432-000-01, 79432-000-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
48d48a33-8187-3c75-e063-6394a90a3bc4aaf83399-9eb5-4ea7-e053-2a95a90a73222026-01-20WarningsExact identifier
spl set id: aaf83399-9eb5-4ea7-e053-2a95a90a7322

Reported adverse events (FAERS/openFDA)#

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