FDA.reportPublic FDA data

Wet Wipe

Manufacturer
Zhejiang quercus daily necessities Co., Ltd
Effective date
2020-07-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:23:52

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

1 PCS NDC 90017-001-01 013013

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038558benzalkonium chloride 0.13 % Medicated PadPSN1
1038558benzalkonium chloride 1.3 MG/ML Medicated PadSCD1
1038558benzalkonium chloride 0.13 % Topical ClothSY1
1038558benzalkonium chloride 0.13 % Topical SwabSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical PadSY1
1038558benzalkonium chloride 0.13 GM per 100 GM Topical SwabSY1
1038558benzalkonium chloride 1 ML per 750 ML Topical SwabSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
90017-001-012022-01-28C16284748780-1d6a99b39-ad71-a426-e053-dadaa90af4c2quercus wet wipes 0.13% BENZALKONIUM CHLORIDE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
90017-001-01Wet Wipe1 in 1 POUCHCLOTH11
90017-001-01Wet Wipe6.5 g in 1 APPLICATORCLOTH6.51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
90017-001WET WIPE (BENZALKONIUM CHLORIDE) CLOTH [ZHEJIANG QUERCUS DAILY NECESSITIES CO., LTD]1Legacy NDC, 2 package rows20200806_aa491803-ef53-1a1b-e053-2995a90ac423.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
90017-00190017-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
POLYSORBATE 207T1F30V5YHIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PHENOXYETHANOLHIE492ZZ3TIACT
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
a8baab66-0b33-297a-e053-2995a90af4d8aa491803-ef53-1a1b-e053-2995a90ac4232020-07-24WarningsExact identifier
spl id: a8baab66-0b33-297a-e053-2995a90af4d8
spl set id: aa491803-ef53-1a1b-e053-2995a90ac423

Reported adverse events (FAERS/openFDA)#

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