Weekender Clean Travel Kit

Manufacturer: Talus Corporation
Effective date: 2021-12-13
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 22:23:24

Label at a glance#

ProductWeekender Clean Travel Kit

Active ingredientBENZALKONIUM CHLORIDE

Label structure7 sections

Dosage and administration

Tear open packet, unfold and use as a washcloth.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.133% w/v

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Use

INDICATIONS & USAGE SECTION

Antiseptic Cleansing of face, hands and body without soap and water. Air dries in seconds.

WARNINGS SECTION

Do Not Use

OTC - DO NOT USE SECTION

In the eyes or apply over alrge areas of the body.

Stop Use

OTC - STOP USE SECTION

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

Caution 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, unfold and use as a washcloth.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Sodium Bicarbonate, Water

Package Labeling:Kit

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Kit2

Package Labeling:81330-000-00

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1043307	benzalkonium chloride 1.33 MG/ML Medicated Pad	benzalkonium chloride 1.33 MG/ML Medicated Pad	SCD Active

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

Weekender Clean Travel Kit
BENZALKONIUM CHLORIDE
Dukal BZK Towelette
SODIUM BICARBONATE
WATER
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
81330-002	81330-002-01
81330-000	81330-000-01

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
Name	UNII	Kind
SODIUM BICARBONATE	8MDF5V39QO	IACT
WATER	059QF0KO0R	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d30d8a59-44a2-5608-e053-2a95a90a0e9b			b8a6a81e-6ede-1795-e053-2995a90aed1d	2021-12-13	Warnings	Exact identifier spl id: d30d8a59-44a2-5608-e053-2a95a90a0e9b spl set id: b8a6a81e-6ede-1795-e053-2995a90aed1d

Reported adverse events (FAERS/openFDA)#

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