FDA.reportPublic FDA data

Antibacterial HAND WIPES

Manufacturer
NUVIK GLOBAL LIMITED
Effective date
2021-11-24
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:25:59

Label at a glance#

ProductAntibacterial HAND WIPES
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

decreases bacteria on skin

Dosage and administration

Adults and children 2 years and over Apply to hands allow to dry without wiping children under 2 years ask a doctor before use

Label contents#

Full prescribing information#

Active-Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

decreases bacteria on skin

Warnings

WARNINGS SECTION

  • For external use only
  • Do not use if you are allergic to any of the ingredients.
  • 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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 2 years and over
  • Apply to hands
  • allow to dry without wiping
  • children under 2 years ask a doctor before use

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

 If swallowed, get medical help or contact a Poison Control Center right away.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aqua, C12-14 Alkyldimethyl, DidecylDimethyl Ammonium Chloride Amines, N-Oxides Sodium Ethylhexyl Sulfate.

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74131-00174131-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
POLIHEXANIDE322U039GMFIACT
SODIUM ETHASULFATE12838560LIIACT
(C10-C16)ALKYLDIMETHYLAMINE OXIDELF6BKC321JIACT
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
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
d18ca6e8-9896-764d-e053-2995a90ac73effecb2ea-bc02-481a-9845-6ca4bc8c8a302021-11-24WarningsExact identifier
spl id: d18ca6e8-9896-764d-e053-2995a90ac73e
spl set id: ffecb2ea-bc02-481a-9845-6ca4bc8c8a30

Reported adverse events (FAERS/openFDA)#

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