KLEENLINE

Manufacturer: Teh Tung Corporation
Effective date: 2020-10-06
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:31:37

Label at a glance#

ProductKLEENLINE

Active ingredientALCOHOL

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)

Contacts and useful links#

PhoneLabel contact1-800-995-4466

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 73%

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.

Other information

STORAGE AND HANDLING SECTION

Store above 0°C (32°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water, Dimethicone, Isopropyl alcohol

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

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.

OTC - QUESTIONS SECTION

Questions? Call 1-800-995-4466

SPL UNCLASSIFIED SECTION

BY WAXIE

FOAM HAND SANITIZER

ETHANOL ALCOHOL

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

Packaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2287765	ethanol 73 % Topical Solution	PSN	1
2287765	ethanol 0.73 ML/ML Topical Solution	SCD	1
2287765	ethanol 73 % Topical Solution	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78168-628-88	2022-01-28	C162847	48780-1	d6a99b39-7d17-a426-e053-dadaa90af4c2	KLEENLiNE ™ FOAM HAND SANITIZER
78168-628-99	2022-01-28	C162847	48780-1	d6a99b39-7d17-a426-e053-dadaa90af4c2	KLEENLiNE ™ FOAM HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78168-628-88	KLEENLINE	1000 mL in 1 BOTTLE	LIQUID	1000		1
78168-628-99	KLEENLINE	3785 mL in 1 BOTTLE	LIQUID	3785		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78168-628	KLEENLINE (ETHYL ALCOHOL) LIQUID [TEH TUNG CORPORATION]	1	Legacy NDC, 2 package rows	20201015_528da66a-0463-457f-845e-ab11581ef7aa.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

KLEENLINE
Ethyl alcohol
ALCOHOL
WATER
DIMETHICONE
ISOPROPYL ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78168-628	78168-628-88, 78168-628-99

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
DIMETHICONE	92RU3N3Y1O	IACT
ISOPROPYL ALCOHOL	ND2M416302	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
abd7a48c-351a-40ee-9a82-553ec42f16a7			528da66a-0463-457f-845e-ab11581ef7aa	2020-10-06	Warnings	Exact identifier spl id: abd7a48c-351a-40ee-9a82-553ec42f16a7 spl set id: 528da66a-0463-457f-845e-ab11581ef7aa

Reported adverse events (FAERS/openFDA)#

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