FDA.reportPublic FDA data

Antibacterial Hand Wipes

Manufacturer
AS Beauty | Hangzhou Glamcos Biotech CO., LTD
Effective date
2020-06-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:21:20

Label at a glance#

ProductAntibacterial Hand Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

Back of Package (Active Ingredients)

OTC - ACTIVE INGREDIENT SECTION

Back of PackageBack of Package

Usage

DOSAGE & ADMINISTRATION SECTION

Rub Cloth Between Hands and let Air Dry

Non Active Ingredients

INACTIVE INGREDIENT SECTION

Water, Phenoxyethanol, Didecylmdimonium Chloride, Propylene Glycol, Chlophenesin

Usage indications

INDICATIONS & USAGE SECTION

Stop uisng if irritation or rash occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of Children

Benzalkonium Chloride

OTC - PURPOSE SECTION

Antibacterial

Warnings

WARNINGS SECTION

For External Use Only

Do no use on wounds or cuts

Keep out of contact of eyes, ears and mouth

Front of Package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front of PackageFront of Package

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74884-220-202022-01-28C16284748780-1d6a99b39-c1ef-a426-e053-dadaa90af4c2a75c6ac5-4079-6978-e053-2995a90a343d

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74884-220-20Antibacterial Hand Wipes20 g in 1 POUCHCLOTH201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74884-220ANTIBACTERIAL HAND WIPES (BENZALKONIUM CHLORIDE) CLOTH [AS BEAUTY]1Legacy NDC, 1 package rows20200715_a75c6ac5-4079-6978-e053-2995a90a343d.zip

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
74884-22074884-220-20

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
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
CHLORPHENESINI670DAL4SZIACT
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PHENOXYETHANOLHIE492ZZ3TIACT

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
a75c6ac5-407a-6978-e053-2995a90a343da75c6ac5-4079-6978-e053-2995a90a343d2020-06-05WarningsExact identifier
spl id: a75c6ac5-407a-6978-e053-2995a90a343d
spl set id: a75c6ac5-4079-6978-e053-2995a90a343d

Reported adverse events (FAERS/openFDA)#

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