ANTIBACTERIAL WIPES

Manufacturer
TISSUE PAPER PRODUCTION & TRADING CO.,LTD
Effective date
2020-08-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:24:50

Label at a glance#

ProductANTIBACTERIAL WIPES
Active ingredientALCOHOL, BENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

For hands washing to decrease bacteria on the skin. May be used on face, arms, legs

Dosage and administration

-Apply thoroughly to hands as desired. -Allow to dry without wiping. -Discard after use -Children under 6 years of age should be supervised when using this product

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

-Ethanol 60%

-Benzalkonium chloride 0.1%

PURPOSE

OTC - PURPOSE SECTION

Antibacterial

Antibacterial

USES:

INDICATIONS & USAGE SECTION

For hands washing to decrease bacteria on the skin. May be used on face, arms, legs

WARNINGS:

WARNINGS SECTION

-For external use only

-When using this product do not use in or near the eyes

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

-Keep out of reach of children

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

-Apply thoroughly to hands as desired.

-Allow to dry without wiping.

-Discard after use

-Children under 6 years of age should be supervised when using this product

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Pure water, Propylene Glycol, Decyl Glucoside, Phenoxyethanol, Benzoic Acid, Citric Acid

SPL UNCLASSIFIED SECTION

Soft Nonwoven Fabric

Non-greasy On Skin

MADE IN VIETNAM

MANUFACTURED & PACKED FOR:

AM PACKAGING CORPORATION LTD

233 BROADWAY, SUITE 2040, NEW YORK, 10279

Hotline: +44 7540757812

Email: alan@ampccorp.com

Web: www.papercanary.net

MFG:

EXP

LOT NO:

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2390359benzalkonium chloride 0.1 % / ethanol 60 % Medicated PadPSN1
2390359benzalkonium chloride 1 MG/ML / ethanol 0.6 MG/ML Medicated PadSCD1
2390359benzalkonium chloride 0.1 % / ethanol 60 % Medicated PadSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79854-100-012022-01-28C16284748780-1d6a99b39-e006-a426-e053-dadaa90af4c2AMPC CART WIPES

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79854-100-01ANTIBACTERIAL WIPES2 in 1 BAGCLOTH21
79854-100-01ANTIBACTERIAL WIPES800 in 1 PACKETCLOTH8001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79854-100ANTIBACTERIAL WIPES (ETHYL ALCOHOL, BENZALKONIUM CHLORIDE) CLOTH [TISSUE PAPER PRODUCTION & TRADING CO.,LTD]1Legacy NDC, 2 package rows20200815_f271addd-3610-4b33-9659-e6581a7b5534.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79854-10079854-100-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
f2695c46-1ea8-4679-9276-54187773fe07f271addd-3610-4b33-9659-e6581a7b55342020-08-13WarningsExact identifier
spl id: f2695c46-1ea8-4679-9276-54187773fe07
spl set id: f271addd-3610-4b33-9659-e6581a7b5534

Reported adverse events (FAERS/openFDA)#

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