BZK AGENT SANITIZER- non alcohol spray sanitizer with additive spray

BZK Agent Sanitizer by

Drug Labeling and Warnings

BZK Agent Sanitizer by is a Otc medication manufactured, distributed, or labeled by Tropical Enterprises International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: Benzalkonium Chloride 0.13%

ASK DOCTOR

Stop use and ask a doctor if irritation or redness develops and persists.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, seek medical attention or contact a Poison Control Center right away.

PURPOSE

Uses: For hand sanitizing to decrease bacteria on the skin. Recommended for repeat use.

QUESTIONS

Questions: 1-800-535-5053

STOP USE

Stop use and ask a doctor if irritation or redness develops and persists.

WHEN USING

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

DOSAGE & ADMINISTRATION

Uses: For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use.

Directions: Wet hands thoroughly with product and allow to dry without wiping.

INACTIVE INGREDIENT

Inactive Ingredients: Water, 2-Phenoxyethanol, Silicon Quaternary Ammonia Salt .75%

WARNINGS

WARNINGS For external use only

SAFE HANDLING WARNING

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

OTHER SAFETY INFORMATION

Other info: Non-staining, may discolor certain fabrics.

INDICATIONS & USAGE

Uses: For hand sanitizing to decrease bacteria on the skin. Recommended for repeat use.

Directions: Wet hands thoroughly with product and allow to dry without wiping.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BZK AGENT SANITIZER 
non alcohol spray sanitizer with additive spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58418-759
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 30 mL

Inactive Ingredients
Ingredient Name	Strength
OCTADECYLDIMETHYL(3-TRIHYDROXYSILYLPROPYL)AMMONIUM CHLORIDE (UNII: GLJ50K866T)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58418-759-08	240 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	07/01/2020

Labeler - Tropical Enterprises International, Inc. (091986179)

Registrant - Tropical Enterprises International, Inc. (091986179)

Establishment
Name	Address	ID/FEI	Business Operations
Tropical Enterprises International, Inc.		091986179	manufacture(58418-759) , pack(58418-759) , label(58418-759)