FDA.reportPublic FDA data

Antibacterial Hand Wipes

Manufacturer
AS Beauty | Hangzhou Glamcos Biotech CO.,LTD
Effective date
2020-05-19
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#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Package BackPackage Back

Usage

DOSAGE & ADMINISTRATION SECTION

Rub cloth completely between hands and let air dry.

Non Active Ingredients

INACTIVE INGREDIENT SECTION

Water, Phenoxyethanol, Didecyldimonium Chloride, Propylene Glycol, Chlorphenesin.

Indications upon usage

INDICATIONS & USAGE SECTION

Stop usage and consult a doctor if a rash or irritation occurs.

Not for Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep away from Children

Product Purpose

OTC - PURPOSE SECTION

Antibacterial

Warnings

WARNINGS SECTION

For External Use Only.

Keep out of Eyes, Ears and Mouth.

Do not use on Open Wounds or Cuts

Front of Package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package FacePackage Face

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74884-120-602022-01-28C16284748780-1d6a99b39-c02a-a426-e053-dadaa90af4c2a604a7ff-938a-5fce-e053-2a95a90aad7e

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74884-120-60Antibacterial Hand Wipes60 g in 1 POUCHCLOTH601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74884-120ANTIBACTERIAL HAND WIPES (BENZALKONIUM CHLORIDE) CLOTH [AS BEAUTY]1Legacy NDC, 1 package rows20200715_a604a7ff-938a-5fce-e053-2a95a90aad7e.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
74884-12074884-120-60

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
PHENOXYETHANOLHIE492ZZ3TIACT
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
CHLORPHENESINI670DAL4SZIACT
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT

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
a604a7ff-938b-5fce-e053-2a95a90aad7ea604a7ff-938a-5fce-e053-2a95a90aad7e2020-05-19WarningsExact identifier
spl id: a604a7ff-938b-5fce-e053-2a95a90aad7e
spl set id: a604a7ff-938a-5fce-e053-2a95a90aad7e

Reported adverse events (FAERS/openFDA)#

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