FDA.reportPublic FDA data

MARVEL BZK ANTISEPTIC WIPE

Manufacturer
Ashtel Studios, Inc.
Effective date
2024-11-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:39:47

Label at a glance#

ProductMARVEL BZK ANTISEPTIC WIPE
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

• To help prevent skin infection in open wounds

Dosage and administration

• Clean the affected area

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• To help prevent skin infection in open wounds

Warnings

WARNINGS SECTION

For external use only

Do not use in the eyes or over large areas of the body.

Ask a doctor before use if you have deep or puncture wounds or serious burns.

Stop use and ask a doctor if irritation or redness develops.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Clean the affected area

Inactive ingredients 

INACTIVE INGREDIENT SECTION

Purified Water, Sodium Bicarbonate

SPL UNCLASSIFIED SECTION

© MARVEL

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BZK ANTISEPTIC WIPEBZK ANTISEPTIC WIPE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN1
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD1
1038558benzalkonium chloride 0.13 % Topical ClothSY1
1038558benzalkonium chloride 0.13 % Topical SwabSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY1
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70108-104-01MARVEL BZK ANTISEPTIC WIPE0.0011 mL in 1 PACKAGECLOTH0.00111
70108-104-01MARVEL BZK ANTISEPTIC WIPE1 in 1 POUCHCLOTH11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70108-104MARVEL BZK ANTISEPTIC WIPE (BENZALKONIUM CHLORIDE) CLOTH [ASHTEL STUDIOS, INC.]1Current NDC, 2 package rows20241130_93ed0bb4-834d-44ca-9c0a-20086fc09ab8.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70108-10470108-104-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
SODIUM BICARBONATE8MDF5V39QOIACT

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
MARVEL BZK ANTISEPTIC WIPEBENZALKONIUM CHLORIDEAshtel Studios, Inc.93ed0bb4-834d-44ca-9c0a-20086fc09ab82024-11-18WarningsExact identifier
ndc (package): 70108-104-01
ndc (product): 70108-104
ndc11 (package): 70108010401
spl id: 56de1eb6-038f-4426-8405-d05613724912
spl set id: 93ed0bb4-834d-44ca-9c0a-20086fc09ab8

Reported adverse events (FAERS/openFDA)#

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