FDA.reportPublic FDA data

Wet Nap Antibacterial Hand Wipes Fresh

Manufacturer
Nice-Pak Products, Inc. | Tongling Jieya Biologic Technology Stock Co., Ltd.
Effective date
2020-06-26
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:24:13

Label at a glance#

ProductWet Nap Antibacterial Hand Wipes Fresh
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Benzalkonium chloride 0.13% w/w

OTC - PURPOSE SECTION

Purpose

Antiseptic handwash

INDICATIONS & USAGE SECTION

Use

For handwashing to decrease bacteria on the skin

WARNINGS SECTION

Warnings

For external use only

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

OTC - DO NOT USE SECTION

Do not use in the eyes

Discontinue use if irritation and redness develop.

If condition persists for more than 72 hours consult a doctor.

DOSAGE & ADMINISTRATION SECTION

Directions

To dispense, lift cover, remove seal, pull center sheet from roll, twist to a point, feed through dispenser hole in cover.

Keep lid closed to prevent moisture loss.

Use as a part of your hand cleansing routine.

Rub product onto hands and allow to dry.

Discard after single use.

REFERENCES SECTION

Other information

Lot No. and Expiration Date. Can be found on canister.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Purified Water, SD Alcohol 40, Sorbic Acid, PPG-2 Hydroxyethyl Cocamide, Disodium EDTA, Aloe Barbadensis Leaf Juice, Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

The Original

Wet-Nap

ANTIBACTERIAL

HAND WIPES

Moisturizes with Aloe

Kills 99.99% of Germs

Fresh Scent

40

Count 5.7 X 7.5 (14.5 X 19.05 cm)

container labelFcontainer labelF

container labelBcontainer labelB

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44385-701144385-7011-1, 44385-7011-2, 44385-7011-3, 44385-7011-4, 44385-7011-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
SORBIC ACIDX045WJ989BIACT
PPG-2 HYDROXYETHYL COCAMIDE34N07GUJ3XIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
ALOE VERA LEAFZY81Z83H0XIACT
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
eca82586-706f-249e-e053-2a95a90a9c23e6f1be09-cb46-41b2-a8ba-2249b6e5f33f2022-11-04WarningsExact identifier
spl set id: e6f1be09-cb46-41b2-a8ba-2249b6e5f33f

Reported adverse events (FAERS/openFDA)#

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