KLEENLINE FOAM HAND SANITIZER- benzalkonium chloride liquid

KLEENLINE FOAM HAND SANITIZER by

Drug Labeling and Warnings

KLEENLINE FOAM HAND SANITIZER 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

Benzalkonium Chloride 0.13%

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.

Inactive ingredients

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

Warnings

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.

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

Other information

Store above 0°C (32°F)

Questions?

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

INGREDIENTS AND APPEARANCE

KLEENLINE FOAM HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78168-618
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78168-618-88	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2021
2	NDC: 78168-618-99	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2021

Labeler - Teh Tung Corporation (023729484)