Antibacterial Hand Wipes

Manufacturer
Osike Cosmetics Co., Ltd.
Effective date
2022-11-29
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:51:55

Label at a glance#

ProductAntibacterial Hand Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure13 sections

Dosage and administration

●Apply to hands, allow to air dry without wiping. ●Children under 6 years of age should be supervised when using this product

Storage and handling

●Store in a cool,dry place. ●Avoid freezing and excessive heat.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.12%

Purpose

OTC - PURPOSE SECTION

Antimicroblal

Use

INDICATIONS & USAGE SECTION

●Hand sanitizer to help reduce bacteria
●For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

●on children less than 2 months old.
●on open skin wounds

OTC - WHEN USING SECTION

When using this product do not get in eyes. If

contact is made rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts.

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

●Apply to hands, allow to air dry without wiping.
●Children under 6 years of age should be supervised when using this product

Other information

STORAGE AND HANDLING SECTION

●Store in a cool,dry place.
●Avoid freezing and excessive heat.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, Phenoxyethanol, Propylene Glycol, Water

800 wipes

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

800 wipes800 wipes

1600 wipes

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1600 wipes1600 wipes

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038741benzalkonium Cl 0.12 % Medicated PadPSN4
1038741benzalkonium chloride 1.2 MG/ML Medicated PadSCD4
1038741benzalkonium chloride 0.12 % Medicated WipeSY4
1038741benzalkonium chloride 0.12 % Topical ClothSY4
1038741benzalkonium chloride 0.12 % Topical SwabSY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79866-005-012024-01-30C16284748780-11030e365-32f3-111a-e063-dadaa90a10e279866-005 Antibacterial Hand Wipes
79866-005-022024-01-30C16284748780-11030e365-32f3-111a-e063-dadaa90a10e279866-005 Antibacterial Hand Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79866-005-01Antibacterial Hand Wipes800 in 1 BAGCLOTH8004
79866-005-02Antibacterial Hand Wipes1600 in 1 BAGCLOTH16004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79866-005ANTIBACTERIAL HAND WIPES (WIPES) CLOTH [OSIKE COSMETICS CO., LTD.]4Legacy NDC, 2 package rows20221130_ab7d6744-9a49-65e6-e053-2995a90a5165.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
79866-00579866-005-01, 79866-005-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
ee99b49b-ef93-7f91-e053-2995a90afa6dab7d6744-9a49-65e6-e053-2995a90a51652022-11-29WarningsExact identifier
spl id: ee99b49b-ef93-7f91-e053-2995a90afa6d
spl set id: ab7d6744-9a49-65e6-e053-2995a90a5165

Reported adverse events (FAERS/openFDA)#

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