KENTEX Hand Sanitizing Wet Wipes

Manufacturer
Kentron Healthcare, Inc. | JIANGSU HANHE DAILY CHEMICALS CO., LTD.
Effective date
2021-11-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:44:45

Label at a glance#

ProductKENTEX Hand Sanitizing Wet Wipes
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Adults and children 2 years and over: apply to hands and allow skin to dry Children under 2 years: ask a doctor before use

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Decrease bacteria on hands

Warnings

WARNINGS SECTION

For external use only

Flammable. Keep away from fire or flame

keep out of eyes. In case of eye contact, immediately flush with water and get medical help

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a poison control immediately

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 2 years and over: apply to hands and allow skin to dry
  • Children under 2 years: ask a doctor before use

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69556-444-802023-01-30C16284748780-1f386c649-eba4-0266-e053-dadaa90a7c1a69556-444-80 Kentex wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69556-444-80KENTEX Hand Sanitizing Wet Wipes80 in 1 CANISTERSOLUTION802

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69556-444KENTEX HAND SANITIZING WET WIPES (ALCOHOL) SOLUTION [KENTRON HEALTHCARE, INC.]2Legacy NDC, 1 package rows20211104_f306104a-0381-4e56-80bc-3ea7f08014eb.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69556-44469556-444-80

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
cfda5ed5-7970-b6e6-e053-2995a90a5136f306104a-0381-4e56-80bc-3ea7f08014eb2021-11-02WarningsExact identifier
spl id: cfda5ed5-7970-b6e6-e053-2995a90a5136
spl set id: f306104a-0381-4e56-80bc-3ea7f08014eb

Reported adverse events (FAERS/openFDA)#

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