PDI Benzalkonium Chloride

Manufacturer
Professional Disposables International, Inc.
Effective date
2012-05-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:47:22

Label at a glance#

ProductPDI Benzalkonium Chloride Antiseptic Towelettes
Active ingredientBenzalkonium Chloride
Label structure9 sections

Dosage and administration

Tear open packet. Unfold and use; discard after single use. Wet hands thoroughly with product and allow to dry without wiping.

Label contents#

Full prescribing information#

Use

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

  • Flammable, keep away from fire or flame.
  • For external use only.
  • If swallowed, get medical help or contact a Poison Control Center right away.
  • Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.
  • Do not use in the eyes.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

SPL UNCLASSIFIED SECTION


  • Tear open packet.
  • Unfold and use; discard after single use.
  • Wet hands thoroughly with product and allow to dry without wiping.

Other information

SPL UNCLASSIFIED SECTION

Lot No. and Expiration Date can be found on back panel of packet.

Dosage

DOSAGE & ADMINISTRATION SECTION


Wet hands thoroughly with product and allow to dry without wiping.

Inactive ingredients

INACTIVE INGREDIENT SECTION

USP Purified Water

SPL UNCLASSIFIED SECTION

Professional Disposables International, Inc.
Orangeburg, NY 10962-1376 - USA - 1-800-999-6423
www.pdipdi.com              Made in USA

Principal Display Panel - 100 Count

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDI
Benzalkonium Chloride
Antiseptic Towelettes


For Professional and Hospital Use

1 Towelette [7.7 x 5.0 in (19.6 x 12.7 cm)] 100 Towelettes per Box

Packet Label
Image of Packet Label
Image of Packet Label
Box Label
Image of Box Label
Image of Box Label

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13% w/w

Purpose

OTC - PURPOSE SECTION

Antiseptic handwash

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10819-3737-12026-01-09C16284748780-19d75b9d0-4957-f424-e053-dadaa90a57cePDI BENZALKONIUM CHLORIDE ANTISEPTIC TOWELETTES
10819-3737-12020-01-31C16284748780-19d75b9d0-4957-f424-e053-dadaa90a57cePDI BENZALKONIUM CHLORIDE ANTISEPTIC TOWELETTES

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10819-3737PDI BENZALKONIUM CHLORIDE ANTISEPTIC TOWELETTES (BZK) CLOTH [PROFESSIONAL DISPOSABLES INTERNATIONAL, INC.]1Legacy NDC20120508_0e606002-5c1e-4822-bb82-8c6df8fca5f6.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Benzalkonium ChlorideACTIVE INGREDIENTF5UM2KM3W71
BENZALKONIUMACTIVE MOIETY7N6JUD5X6Y1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10819-373710819-3737-1

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
Benzalkonium ChlorideF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT

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
435689f5-32f6-b82c-e063-6394a90a0c320e606002-5c1e-4822-bb82-8c6df8fca5f62025-11-11WarningsExact identifier
spl set id: 0e606002-5c1e-4822-bb82-8c6df8fca5f6

Reported adverse events (FAERS/openFDA)#

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