KLEENLINE- ethyl alcohol liquid

KLEENLINE by

Drug Labeling and Warnings

KLEENLINE by is a Otc medication manufactured, distributed, or labeled by Teh Tung Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient 

Ethyl Alcohol 73%

Purpose

Antimicrobial

Uses

Hand sanitizing to help reduce bacteria on the skin

Recommended for repeated use

Directions

Apply liberally to the hands and gently rub until dry.

Other information

Store above 0°C (32°F)

Inactive ingredients

Purified water, Dimethicone, Isopropyl alcohol

Warnings

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.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

QUESTIONS

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

INGREDIENTS AND APPEARANCE

KLEENLINE 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78168-628
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	73 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
ISOPROPYL ALCOHOL (UNII: ND2M416302)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78168-628-88	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/15/2020
2	NDC: 78168-628-99	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/15/2020

Labeler - Teh Tung Corporation (023729484)