Antibacterial Hand Wipes

Manufacturer
INOVAGEL MÉXICO, S.A. DE C.V.
Effective date
2024-01-17
Label type
HUMAN OTC DRUG LABEL
Version
17
Source
legacy-cache
Hydrated at
2026-08-01 21:14:05

Label at a glance#

ProductAntibacterial Hand Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

Adults and children 6 years and older: Rub wipe thoroughly over all surfaces of hands and allow to dry Children under 6 years: Should be supervised when using this product

Storage and handling

To dispose: Place in wastebasket after use. Do not flush

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.15%.

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

To help reduce bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

When using this product

  • Do not use in or near the eyes.
  • In case of contact, rinse eyes thoroughly with water.

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs.

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

  • Adults and children 6 years and older: Rub wipe thoroughly over all surfaces of hands and allow to dry
  • Children under 6 years: Should be supervised when using this product

Other information

STORAGE AND HANDLING SECTION

  • To dispose: Place in wastebasket after use.
  • Do not flush

Inactive ingredients

INACTIVE INGREDIENT SECTION

Propylene glycol, Water.

Package container Antibacterial Hand Wipes, alcohol free

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 81575-002-08 Container 120 ETIQUETA_BZK120ETIQUETA_BZK120

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81575-00281575-002-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
2a33ff82-49de-7aaa-e063-6294a90a1281be242c78-e7de-6148-e053-2a95a90a007e2024-12-26WarningsExact identifier
spl set id: be242c78-e7de-6148-e053-2a95a90a007e

Reported adverse events (FAERS/openFDA)#

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