WET WIPE

Manufacturer
Osike Cosmetics Co., Ltd.
Effective date
2020-12-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:35:43

Label at a glance#

ProductWET WIPE
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 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, between 15°C-30°C(59°F-86°F) ●Avoid freezing and excessive heat above 40°C(104°F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13% ……………………………………………...Antimicroblal

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

●in children less than 2 months old.

●on open skin wounds

OTC - WHEN USING SECTION

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition

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, between 15°C-30°C(59°F-86°F)

●Avoid freezing and excessive heat above 40°C(104°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Extract, Alpha-Tocopherol, Fragrance, Glycerin,

Phenoxyethanol, Propylene Glycol, Purified Water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

79866-011-01 40

79866-011-01 4079866-011-01 40

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79866-011-012022-01-28C16284748780-1d6a99b39-e7b1-a426-e053-dadaa90af4c279866-011 WET WIPE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79866-011-01WET WIPE40 in 1 DRUMCLOTH401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79866-011WET WIPE (BIOPURE ANTIBACTERIAL HAND WIPE CITRUS SCENT 40 CT) CLOTH [OSIKE COSMETICS CO., LTD.]1Legacy NDC, 1 package rows20201223_b70a7bc4-50e8-60fb-e053-2995a90a3214.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
79866-01179866-011-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
b70a8784-e2e4-f08f-e053-2995a90a4a58b70a7bc4-50e8-60fb-e053-2995a90a32142020-12-22WarningsExact identifier
spl id: b70a8784-e2e4-f08f-e053-2995a90a4a58
spl set id: b70a7bc4-50e8-60fb-e053-2995a90a3214

Reported adverse events (FAERS/openFDA)#

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