WIPE OUT Antibacterial Wipes

Manufacturer
ZHEJIANG BINGER NONWOVEN CO., LTD.
Effective date
2022-01-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:46:58

Label at a glance#

ProductWIPE OUT Antibacterial Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Dosage and administration

■I Wet hands thoroughly with product and allow to dry without wiping■I for children| under 6, use only under adult supervision ■not recommended for infants Other information 1 1 Keep containers tightly closed in a dry, cool and well-ventilated place. ■Recommended storage temperature: 32°F to 104°F (0°C to 40°C)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiacterial

USE

INDICATIONS & USAGE SECTION

To decrease bacteria on the
skin that could cause disease

Warning

WARNINGS SECTION

For external use only.
When using this product
■Keep out of eyes. In case
of contact with eyes, flush
thoroughly with water.
■Avoid contact with broken
skin
Stop use and ask a doctor if
■iritation and redness
develop■lcondition persists
for more than 72 houirs.

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

■I Wet hands thoroughly
with product and allow to dry
without wiping■I for children|
under 6, use only under
adult supervision
■not recommended for
infants
Other information
1 1 Keep containers tightly
closed in a dry, cool and
well-ventilated place.
■Recommended storage
temperature: 32°F to 104°F
(0°C to 40°C)

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf juice,
fragrance, phenoxyethanol,
polysorbate 20, propylene
glycol, tocopheryl acetate,
water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

003003

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN3
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD3
1038558benzalkonium chloride 0.13 % Topical ClothSY3
1038558benzalkonium chloride 0.13 % Topical SwabSY3
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY3
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY3
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY3

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76896-003-01WIPE OUT Antibacterial Wipes10 in 1 BAGCLOTH103
76896-003-01WIPE OUT Antibacterial Wipes4.9 g in 1 POUCHCLOTH4.93
76896-003-02WIPE OUT Antibacterial Wipes20 in 1 BAGCLOTH203
76896-003-02WIPE OUT Antibacterial Wipes4.9 g in 1 POUCHCLOTH4.93
76896-003-03WIPE OUT Antibacterial Wipes100 in 1 BAGCLOTH1003
76896-003-03WIPE OUT Antibacterial Wipes4.9 g in 1 POUCHCLOTH4.93
76896-003-04WIPE OUT Antibacterial Wipes4.9 g in 1 POUCHCLOTH4.93
76896-003-04WIPE OUT Antibacterial Wipes50 in 1 BAGCLOTH503
76896-003-05WIPE OUT Antibacterial Wipes4.9 g in 1 POUCHCLOTH4.93
76896-003-05WIPE OUT Antibacterial Wipes60 in 1 BOTTLECLOTH603
76896-003-06WIPE OUT Antibacterial Wipes4.9 g in 1 POUCHCLOTH4.93
76896-003-06WIPE OUT Antibacterial Wipes80 in 1 BOTTLECLOTH803
76896-003-07WIPE OUT Antibacterial Wipes4.9 g in 1 POUCHCLOTH4.93
76896-003-07WIPE OUT Antibacterial Wipes100 in 1 BOTTLECLOTH1003
76896-003-08WIPE OUT Antibacterial Wipes120 in 1 BOTTLECLOTH1203
76896-003-08WIPE OUT Antibacterial Wipes4.9 g in 1 POUCHCLOTH4.93
76896-003-09WIPE OUT Antibacterial Wipes1000 in 1 BOTTLECLOTH10003
76896-003-09WIPE OUT Antibacterial Wipes4.9 g in 1 POUCHCLOTH4.93
76896-003-10WIPE OUT Antibacterial Wipes4.9 g in 1 POUCHCLOTH4.93
76896-003-10WIPE OUT Antibacterial Wipes80 in 1 BAGCLOTH803

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76896-003WIPE OUT ANTIBACTERIAL WIPES (BENZALKONIUM CHLORIDE) CLOTH [ZHEJIANG BINGER NONWOVEN CO., LTD.]3Legacy NDC, 20 package rows20220115_a88ccebc-cb18-cfc1-e053-2a95a90a0cdf.zip

Products#

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

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NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
d59a0890-97c8-6943-e053-2995a90a47aca88ccebc-cb18-cfc1-e053-2a95a90a0cdf2022-01-15WarningsExact identifier
spl id: d59a0890-97c8-6943-e053-2995a90a47ac
spl set id: a88ccebc-cb18-cfc1-e053-2a95a90a0cdf

Reported adverse events (FAERS/openFDA)#

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