KENTEX Instant Hand Sanitizer with Aloe Vera

Manufacturer
Kentron Healthcare, Inc. | JIANGSU HANHE DAILY CHEMICALS CO., LTD.
Effective date
2021-11-02
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:44:43

Label at a glance#

ProductKENTEX Instant Hand Sanitizer with Aloe Vera
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Squeeze on hands. Rub hands together until dry

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antimicrobial

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

  • Squeeze on hands. Rub hands together until dry

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Carbomer, Triethanolamine, Glycerin, Aloe Vera Gel, Propylene Glycol, Vitamin E

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69556-333-02KENTEX Instant Hand Sanitizer with Aloe Vera60 mL in 1 BOTTLESOLUTION603
69556-333-08KENTEX Instant Hand Sanitizer with Aloe Vera236 mL in 1 BOTTLESOLUTION2363
69556-333-16KENTEX Instant Hand Sanitizer with Aloe Vera500 mL in 1 BOTTLESOLUTION5003
69556-333-32KENTEX Instant Hand Sanitizer with Aloe Vera1000 mL in 1 BOTTLESOLUTION10003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69556-333KENTEX INSTANT HAND SANITIZER WITH ALOE VERA (ALCOHOL) SOLUTION [KENTRON HEALTHCARE, INC.]3Legacy NDC, 4 package rows20211104_42e8d19b-0cd4-4830-b872-52511731498a.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
69556-33369556-333-02, 69556-333-16, 69556-333-32, 69556-333-08

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
cfda5ed5-7971-b6e6-e053-2995a90a513642e8d19b-0cd4-4830-b872-52511731498a2021-11-02WarningsExact identifier
spl id: cfda5ed5-7971-b6e6-e053-2995a90a5136
spl set id: 42e8d19b-0cd4-4830-b872-52511731498a

Reported adverse events (FAERS/openFDA)#

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