FDA.reportPublic FDA data

Mediclean Sanitizing Wipes

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 21:20:56

Label at a glance#

ProductMediclean Sanitizing Wipes
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 right away. Children under 6 years of age should be supervised whenusing . MEDICLEAN

Directions:

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

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

Package Labeling:84

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:120

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79432-001MEDICLEAN SANITIZING WIPES (BENZALKONIUM CHLORIDE) CLOTH [INDUSTRIAS MAQUÍN, S.A. DE C.V.]2Legacy NDC20231115_b0737388-cbd2-815c-e053-2995a90a73d4.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79432-00179432-001-01, 79432-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
N-(3-AMINOPROPYL)-N-DODECYL-1,3-PROPANEDIAMINEPCJ6308JUEIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PHENOXYETHANOLHIE492ZZ3TIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
GLYCERINPDC6A3C0OXIACT
SODIUM COCOAMPHOACETATEW7Q5E87674IACT
ISOPROPYL ALCOHOLND2M416302IACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
EDETATE SODIUMMP1J8420LUIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
48d5101b-f554-772a-e063-6294a90a520cb0737388-cbd2-815c-e053-2995a90a73d42026-01-20WarningsExact identifier
spl set id: b0737388-cbd2-815c-e053-2995a90a73d4

Reported adverse events (FAERS/openFDA)#

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