FDA.reportPublic FDA data

Travel Hand Wipes Dispenser Kit

Manufacturer
ZOKU LLC
Effective date
2022-09-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:53:53

Label at a glance#

ProductTravel Hand Wipes Dispenser Kit
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

Sanitizing Hand Wipes to helps decrease bacteria on the skin. Recommended for single use.

Dosage and administration

Wipe liberally over the hands & body, rub into skin until dry.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic/Hand & Skin

Uses

INDICATIONS & USAGE SECTION

  • Sanitizing Hand Wipes to helps decrease bacteria on the skin.
  • Recommended for single use.

Warnings

WARNINGS SECTION

  • Do not freeze. For external use only.

Do not use 

OTC - DO NOT USE SECTION

  • in ears, eyes or mouth.
  • Avoid contact with the eyes. In case of contact, flush eyes with water.

Stop use and ask a doctor 

OTC - STOP USE SECTION

  • if redness or irritation develop and persist for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • Children should be supervised when using this product.
  • If swallowed, get medical help or contact Poison Control Centre immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wipe liberally over the hands & body, rub into skin until dry.

Other information

SPL UNCLASSIFIED SECTION

  • Store at room temperature.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Propanediol, Fragrance, Glycol, Cetylpyridinium Chloride, Phenoxyethanol, Glycerin, Ethylhexylglycerin.

Questions?

OTC - QUESTIONS SECTION

1-201-604-1253

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82389-01282389-012-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
PROPANEDIOL5965N8W85TIACT
ETHYLENE GLYCOLFC72KVT52FIACT
CETYLPYRIDINIUM CHLORIDED9OM4SK49PIACT
PHENOXYETHANOLHIE492ZZ3TIACT
GLYCERINPDC6A3C0OXIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
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
e88f0f83-1b8d-d5cb-e053-2995a90a05707acb2d99-ca76-4853-9a06-3585d226eba62022-09-13WarningsExact identifier
spl id: e88f0f83-1b8d-d5cb-e053-2995a90a0570
spl set id: 7acb2d99-ca76-4853-9a06-3585d226eba6

Reported adverse events (FAERS/openFDA)#

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