Antiseptic Towelette

Manufacturer: Honeywell Safety Products USA, Inc
Effective date: 2024-01-12
Label type: HUMAN OTC DRUG LABEL
Version: 9
Source: legacy-cache
Hydrated at: 2026-08-01 21:14:27

Label at a glance#

ProductAntiseptic Towelette

Active ingredientBENZALKONIUM CHLORIDE

Label structure9 sections

Indications and uses

Antiseptic cleansing of face, hands, and body without soap and water

Dosage and administration

tear open packet and use as a washcloth

Contacts and useful links#

PhoneLabel contact1-800-430-5490

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13% w/v

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Uses

INDICATIONS & USAGE SECTION

Antiseptic cleansing of face, hands, and body without soap and water

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

in the eyes or over large areas of the body
on mucous membranes
on irritated skin
in case of deep puncture wounds, animal bites or serious burns, consult a doctor
longer than 1 week unless directed by a doctor

Stop use and ask a doctor if

OTC - STOP USE SECTION

if irritation, redness or other symptoms develop

the condition persists or gets worse

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

tear open packet and use as a washcloth

Other information

SPL UNCLASSIFIED SECTION

store at room temperature 15 ⁰ to 30 ⁰C (59 ⁰ - 86 ⁰F)
do not reuse towelette

Inactive ingredients

INACTIVE INGREDIENT SECTION

water

Questions

OTC - QUESTIONS SECTION

1-800-430-5490

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Antiseptic Towelettes

Products#

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

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

Antiseptic Towelette
Benzalkonium chloride
WATER
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0498-0501	0498-0501-34, 0498-0501-37, 0498-0501-00

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

Source Document#

Source XML · Source PDF

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
1a1690ef-d155-85c6-e063-6294a90a6f8c			60e14eac-dee7-0f29-e053-2a91aa0a2bdd	2024-06-04	Warnings	Exact identifier spl set id: 60e14eac-dee7-0f29-e053-2a91aa0a2bdd

Reported adverse events (FAERS/openFDA)#

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