KLEENLINE FOAM HAND SANITIZER

Manufacturer
Teh Tung Corporation
Effective date
2021-03-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:38:52

Label at a glance#

ProductKLEENLINE FOAM HAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

• Hand sanitizing to help reduce bacteria on the skin • Recommended for repeated use

Dosage and administration

Apply liberally to the hands and gently rub until dry.

Storage and handling

Store above 0°C (32°F)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

• Hand sanitizing to help reduce bacteria on the skin

• Recommended for repeated use

Directions

DOSAGE & ADMINISTRATION SECTION

Apply liberally to the hands and gently rub until dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water, D-glucopyranose, Oligomeric, Decyl octyl glycosides, Glycerol, Methylisothiazolinone and Citric acid

Warnings

WARNINGS SECTION

For external use only.

When using this product avoid contact with the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or redness 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 immediately.

Other information

STORAGE AND HANDLING SECTION

Store above 0°C (32°F)

Questions?

OTC - QUESTIONS SECTION

Call 1-800-995-4466

SPL UNCLASSIFIED SECTION

BZK FORMULA

INSTANTLY KILLS 99.99% OF TESTED GERMS

FRAGRANCE-FREE

PROUDLY MADE IN USA

Distributed by:

WAXIE Sanitary Supply

San Diego, CA 92123

*Patented formula effectively eliminates 99.99% of tested germs, bacteria and viruses in as little as 15 seconds; long-term protection for up to 12 hrs.

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020365benzalkonium chloride 0.13 % Topical FoamPSN1
1020365benzalkonium chloride 1.3 MG/ML Topical FoamSCD1
1020365benzalkonium chloride 0.13 % Topical FoamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78168-618-882023-01-30C16284748780-1f386c649-9e2b-0266-e053-dadaa90a7c1aKLEENLiNE ™ BY WAXIE FOAM HAND SANITIZER
78168-618-992023-01-30C16284748780-1f386c649-9e2b-0266-e053-dadaa90a7c1aKLEENLiNE ™ BY WAXIE FOAM HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78168-618-88KLEENLINE FOAM HAND SANITIZER1000 mL in 1 BOTTLELIQUID10001
78168-618-99KLEENLINE FOAM HAND SANITIZER3785 mL in 1 BOTTLELIQUID37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78168-618KLEENLINE FOAM HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [TEH TUNG CORPORATION]1Legacy NDC, 2 package rows20210311_bc0c8064-7e13-446d-9f3e-72de682e751c.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
78168-61878168-618-88, 78168-618-99

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
e769a3a1-a68c-45c8-be73-68e762049787bc0c8064-7e13-446d-9f3e-72de682e751c2021-03-01WarningsExact identifier
spl id: e769a3a1-a68c-45c8-be73-68e762049787
spl set id: bc0c8064-7e13-446d-9f3e-72de682e751c

Reported adverse events (FAERS/openFDA)#

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