FDA.reportPublic FDA data

ANTISEPTIC WIPE

Manufacturer
Taizhou Kangping Medical Science And Technology Co., Ltd
Effective date
2017-08-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:14:17

Label at a glance#

ProductANTISEPTIC WIPE
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13% v/v

Purpose

Antiseptic

OTC - PURPOSE SECTION

First aid antiseptic to help prevent skin infection in:

  • Minor Cuts
  • Scrapes
  • Burns
  • Antiseptic Cleasing
  • Perineal and maternity care

WARNINGS SECTION

For External Use Only.

OTC - DO NOT USE SECTION

Do not use

  • As an antiseptic for more than 1 week
  • In the eyes
  • Over large areas of the body

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

  • Deep or pucture wounds
  • Animal bites
  • Serious burns

OTC - STOP USE SECTION

Stop use

  • If irritation and redness develop
  • If condition persists more than 72 hours, consult a physician.

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.

INDICATIONS & USAGE SECTION

Directions

  • Tear at notch
  • Remove towelette
  • Use only once

As a first aid antiseptic

  • Clean affected area
  • Apply 1 to 3 times daily
  • May be covered with a sterile bandage
  • If bandaged, let dry first

OTHER SAFETY INFORMATION

Other information

  • Store at room temperature
  • Avoid excessive heat

INACTIVE INGREDIENT SECTION

Inactive ingredients

Water

DOSAGE & ADMINISTRATION SECTION

ANTISEPTIC WIPE

2in x 2.4in / 5cm x 6cm

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BZKBZK

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71310-100-012024-12-07C16284748780-19d75b9d0-5fe9-f424-e053-dadaa90a57ce55ddf0fe-94e1-5fbd-e054-00144ff8d46c
71310-100-012020-01-31C16284748780-19d75b9d0-5fe9-f424-e053-dadaa90a57ce55ddf0fe-94e1-5fbd-e054-00144ff8d46c

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
71310-10071310-100-01

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
289fbf8a-3752-88e4-e063-6394a90a619955ddf0fe-94e1-5fbd-e054-00144ff8d46c2024-12-06WarningsExact identifier
spl set id: 55ddf0fe-94e1-5fbd-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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