Wet Wipe

Manufacturer
Quzhou Zefeng Import& Export Co., Ltd.
Effective date
2020-09-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:28:34

Label at a glance#

ProductWet Wipe
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Dosage and administration

For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

USE

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin.
Recommended for repeated use.

Warning

WARNINGS SECTION

For external use only
When using this product, avoid contact with the eyes.
In case of contact, flush eyes thoroughly with water.
Stop use and ask a doctor if irritation and redness develop.

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

For hand sanitizing to decrease bacteria on the skin.
Recommended for repeated use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Propylene Glycol, Polysorbate 20, Phenoxyethanol.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

75 PCS NDC 80332-001-01 zefeng benzefeng ben

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN2
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD2
1038558benzalkonium chloride 0.13 % Topical ClothSY2
1038558benzalkonium chloride 0.13 % Topical SwabSY2
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY2
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY2
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80332-001-012022-01-28C16284748780-1d6a99b39-7bbd-a426-e053-dadaa90af4c2zefeng wet wipes 0.13% BENZALKONIUM CHLORIDE
80332-001-022022-01-28C16284748780-1d6a99b39-7bbd-a426-e053-dadaa90af4c2zefeng wet wipes 0.13% BENZALKONIUM CHLORIDE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80332-001-01Wet Wipe75 in 1 POUCHCLOTH752
80332-001-01Wet Wipe1.5 g in 1 APPLICATORCLOTH1.52
80332-001-02Wet Wipe1.5 g in 1 APPLICATORCLOTH1.52
80332-001-02Wet Wipe75 in 1 PAILCLOTH752

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80332-001WET WIPE (BENZALKONIUM CHLORIDE) CLOTH [QUZHOU ZEFENG IMPORT& EXPORT CO., LTD.]2Legacy NDC, 4 package rows20200907_ae8ed13d-9ae4-864e-e053-2995a90aeaba.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80332-00180332-001-01, 80332-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
ae8ed13d-9acc-864e-e053-2995a90aeabaae8ed13d-9ae4-864e-e053-2995a90aeaba2020-09-05WarningsExact identifier
spl id: ae8ed13d-9acc-864e-e053-2995a90aeaba
spl set id: ae8ed13d-9ae4-864e-e053-2995a90aeaba

Reported adverse events (FAERS/openFDA)#

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