FDA.reportPublic FDA data

Handy Solutions First Aid Kit Antiseptic Towelette

Manufacturer
Navajo Manufacturing Company Inc.
Effective date
2019-11-07
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-02 00:02:35

Label at a glance#

ProductHandy Solutions First Aid Kit Antiseptic Towelette
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

First aid to help prevent infection in:  minor cuts scrapes burns

Dosage and administration

Tear open packet. unfold towelette and cleanse area as needed. may be covered with a sterile bandage

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride, 0.1% w/v

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Uses

INDICATIONS & USAGE SECTION

First aid to help prevent infection in: 

  • minor cuts
  • scrapes
  • burns

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • in the eyes
  • over large areas of the body
  • if you are allergic to any of the ingredients
  • longer than 1 week unless directed by a doctor

Ask a doctor before use if you have deep

OTC - ASK DOCTOR SECTION

or puncture wounds, animal bites, or serious burns

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition persists or gets worse
  • a rash or other allergic reaction develops

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 towelette and cleanse area as needed.
  • may be covered with a sterile bandage

Other Information

SPL UNCLASSIFIED SECTION

  • store at 15° to 25° C (59° to 77°F)
  • do not use if packet is opened or torn
  • do not freeze

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Distilled Water

Questions or comments?

OTC - QUESTIONS SECTION

call toll-free 1-800-525-5097

​Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

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
67751-19067751-190-02
67751-03667751-036-02

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
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
96c7bd49-27bd-574f-e053-2a95a90ac334696e1e42-1103-0863-e053-2991aa0a3b2c2019-11-07WarningsExact identifier
spl id: 96c7bd49-27bd-574f-e053-2a95a90ac334
spl set id: 696e1e42-1103-0863-e053-2991aa0a3b2c

Reported adverse events (FAERS/openFDA)#

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