FDA.reportPublic FDA data

Antibacterial Hand Wipes

Manufacturer
AS Beauty | Hangzhou Glamcos Biotech CO.,LTD
Effective date
2020-09-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:33:41

Label at a glance#

ProductAntibacterial Hand Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

Actives and Ingredients

OTC - ACTIVE INGREDIENT SECTION

Back of PackageBack of Package

How To Use

DOSAGE & ADMINISTRATION SECTION

Rub cloth between both hands thouroughly, and let air dry.

Non Active Ingredients.

INACTIVE INGREDIENT SECTION

Inactive Ingredients Water (Aqua), Propylene Glycol, Didecyldimonium Chloride, Chlorphenesin, Phenoxyethanol, PEG-40 Hydrogenated Castor Oil, Sambucus Nigra Oil, Echinacea Purpurea Extract

Usage Indications

INDICATIONS & USAGE SECTION

Stop using Wipes if rash or irritation occurs.

Keep Out Of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out of Reach of Children

Actives 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.

FACE OF PACKAGE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FrontFront

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74884-121-012022-01-28C16284748780-1d6a99b39-611a-a426-e053-dadaa90af4c2Antibacterial Wipe

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74884-121-01Antibacterial Hand Wipes1 g in 1 POUCHCLOTH11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74884-121ANTIBACTERIAL HAND WIPES (BENZALKONIUM CHLORIDE) CLOTH [AS BEAUTY]1Legacy NDC, 1 package rows20201115_af5f012f-146a-6d24-e053-2a95a90aabdb.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74884-12174884-121-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
DIDECYLDIMONIUM CHLORIDEJXN40O9Y9BIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
SAMBUCUS NIGRA SEED OILZZV3NWA4A3IACT
CHLORPHENESINI670DAL4SZIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ECHINACEA PURPUREAQI7G114Y98IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT

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
af5f012f-146b-6d24-e053-2a95a90aabdbaf5f012f-146a-6d24-e053-2a95a90aabdb2020-09-15WarningsExact identifier
spl id: af5f012f-146b-6d24-e053-2a95a90aabdb
spl set id: af5f012f-146a-6d24-e053-2a95a90aabdb

Reported adverse events (FAERS/openFDA)#

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