FDA.reportPublic FDA data

First Aid Only BZK Antiseptic Towelette

Manufacturer
Acme United Corporation | Acme Uited Corporation
Effective date
2024-11-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:50:00

Label at a glance#

ProductFirst Aid Only BZK Antiseptic Towelette
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Indications and uses

Uses For handwashing to decrease bacteria on the skin

Dosage and administration

Directions Tear open packet,unfold and use as a washcloth

Storage and handling

Other Information Store at room temperature: 15° -30°C (59° -86°F)

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride, 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Uses For handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

Warnings For external use only.

Do not use

OTC - DO NOT USE SECTION

Do Not Use in the eyes or apply over large areas of the body.

Stop Use

OTC - STOP USE SECTION

Stop use if irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse.

Keep out of reach of children. .

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

Directions Tear open packet,unfold and use as a washcloth

Other Information

STORAGE AND HANDLING SECTION

Other Information Store at room temperature: 15° -30°C (59° -86°F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients Distilled water

Package Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label ImageLabel Image

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0924-7111FIRST AID ONLY BZK ANTISEPTIC TOWELETTE (BENZALKONIUM CHLORIDE) PATCH [ACME UNITED CORPORATION]3Legacy NDC20241109_504b7eca-eec6-31f2-e054-00144ff8d46c.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0924-71110924-7111-00
71310-711

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
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
35bc6e87-7807-59f7-e063-6394a90aab57504b7eca-eec6-31f2-e054-00144ff8d46c2025-06-03WarningsExact identifier
spl set id: 504b7eca-eec6-31f2-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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