Antiseptic Wipe

Manufacturer
Total Resources
Effective date
2022-11-18
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 23:51:42

Label at a glance#

ProductAntiseptic Wipe
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Dosage and administration

Tear open packet, unfold, and use as a washcloth.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride, 0.13%

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Use

INDICATIONS & USAGE SECTION

Antiseptic cleansing of face, hands and body without the use of soap and water. Air dries in seconds.

Warnings

WARNINGS SECTION

Do not use in the eyes or apply over large areas of the body.

Stop use if

OTC - STOP USE SECTION

irritation, redness or other symptoms develop. Cosult a doctor if the condition persists or worsens.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, seek medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Tear open packet, unfold, and use as a washcloth.

Other information

SPL UNCLASSIFIED SECTION

Store at room temperature 59° - 86°F (15° - 30°C)

Inactive ingredient

INACTIVE INGREDIENT SECTION

water

Questions?

OTC - QUESTIONS SECTION

Call 1-888-771-7824

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BZK WipesBZK Wipes

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
55550-210-702024-01-30C16284748780-11030e365-5505-111a-e063-dadaa90a10e2TR-1331 NDC 55550-210-70 Antiseptic Wipe

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55550-210-70Antiseptic Wipe1 mg in 1 PACKETLIQUID15
55550-210-70Antiseptic Wipe1000 in 1 CASELIQUID10005

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55550-210ANTISEPTIC WIPE (BZK ANTISEPTIC WIPE) LIQUID [TOTAL RESOURCES]5Legacy NDC, 2 package rows20221119_7978430f-9408-3516-e053-2a91aa0aa62d.zip

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
55550-21055550-210-70

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 · Source PDF

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
edc14d28-1688-1d0d-e053-2a95a90a49247978430f-9408-3516-e053-2a91aa0aa62d2022-11-18WarningsExact identifier
spl id: edc14d28-1688-1d0d-e053-2a95a90a4924
spl set id: 7978430f-9408-3516-e053-2a91aa0aa62d

Reported adverse events (FAERS/openFDA)#

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