Defender Collection

Manufacturer
Tiger Hospitality, LLC dba A1 American
Effective date
2020-06-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:18:42

Label at a glance#

ProductDefender Collection
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Dosage and administration

Tear V notch located on top of the plastic bag. Pull out the first wipe approximately 6 to 8 inches from the center of the roll. Place entire bag inside of center pull dispenser. Thread the wipe through the opening on the dispenser. Close the lid of the dispenser. Wipe dispensing tension may be adjusted on the top of the dispenser. Dispenser must be mounted with wipes dispensing up. Apply topically to the skin Rec...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.
When using this product do not get into eyes. If contact occurs, rinse thoroughly with water.
Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Tear V notch located on top of the plastic bag.
  • Pull out the first wipe approximately 6 to 8 inches from the center of the roll.
  • Place entire bag inside of center pull dispenser.
  • Thread the wipe through the opening on the dispenser.
  • Close the lid of the dispenser. Wipe dispensing tension may be adjusted on the top of the dispenser. Dispenser must be mounted with wipes dispensing up.
  • Apply topically to the skin
  • Recommended for repeated use.
  • Dries in seconds.
  • For children under 6, use only under adult supervision. Not recommended for infants
  • Discard wipe in trash receptable after use. Do not flush

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Water(Aqua), Fragrance(Parfum), Phenoxyethanol, Polysorbate 20, Propylene Glycol, Tocopheryl Acetate

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN1
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD1
1038558benzalkonium chloride 0.13 % Topical ClothSY1
1038558benzalkonium chloride 0.13 % Topical SwabSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY1
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78940-001-01Defender Collection0.0042 g in 1 POUCHSWAB0.00421
78940-001-02Defender Collection0.0042 g in 1 POUCHSWAB0.00421
78940-001-02Defender Collection50 in 1 BAGSWAB501
78940-001-03Defender Collection80 in 1 BAGSWAB801
78940-001-03Defender Collection0.0042 g in 1 POUCHSWAB0.00421
78940-001-04Defender Collection0.0042 g in 1 POUCHSWAB0.00421
78940-001-04Defender Collection900 in 1 BAGSWAB9001
78940-001-05Defender Collection1000 in 1 BAGSWAB10001
78940-001-05Defender Collection0.0042 g in 1 POUCHSWAB0.00421
78940-001-06Defender Collection0.0042 g in 1 POUCHSWAB0.00421
78940-001-06Defender Collection1200 in 1 BAGSWAB12001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78940-001DEFENDER COLLECTION (BENZALKONIUM CHLORIDE) SWAB [TIGER HOSPITALITY, LLC DBA A1 AMERICAN]1Legacy NDC, 11 package rows20200623_cb2958d3-b6ee-4df1-850e-b7fcbe719bcb.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78940-00178940-001-01, 78940-001-02, 78940-001-03, 78940-001-04, 78940-001-05, 78940-001-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

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
26b7406c-ca95-4b56-9bdb-97b18a6011c2cb2958d3-b6ee-4df1-850e-b7fcbe719bcb2020-06-18WarningsExact identifier
spl id: 26b7406c-ca95-4b56-9bdb-97b18a6011c2
spl set id: cb2958d3-b6ee-4df1-850e-b7fcbe719bcb

Reported adverse events (FAERS/openFDA)#

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