FDA.reportPublic FDA data

Antiseptic Towel Benzalkonium Chloride

Manufacturer
Global-C Nederland B.V.
Effective date
2020-08-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:18:15

Label at a glance#

ProductAntiseptic Towel Benzalkonium Chloride
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only. Avoid any contact with eyes, ears or mouth.

Should accidental contact with eyes occur, rinse eyes thoroughly wiht water

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Irritation and redness develop
  • condition persists for more than 72 hours

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.

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product and allow to dry without wiping

Other information

SPL UNCLASSIFIED SECTION

Store below 77 °F  (25 °C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

cellulose fiber, polyester, water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

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
78657-00678657-006-01

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
POWDERED CELLULOSESMD1X3XO9MIACT
WATER059QF0KO0RIACT
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
0f3ef88d-4c14-9e15-e063-6394a90a2857ad2b5770-b9c5-4476-e053-2995a90a9af72024-01-18WarningsExact identifier
spl set id: ad2b5770-b9c5-4476-e053-2995a90a9af7

Reported adverse events (FAERS/openFDA)#

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