BZK HAND SANITIZER spray

BZK Hand Sanitizer by

Drug Labeling and Warnings

BZK Hand 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

Ethyl Alcohol 62% w/w

PURPOSE

Purpose..... Antiseptic

INDICATIONS AND USAGE

Uses: For handwashing to decrease bacteria on the skin

DOSAGE AND ADMINISTRATION

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

INACTIVE INGREDIENT

Inactive Ingredients Water, Glycerin, Lavandin Grosso (Lavender) Oil, Polysorbate 20,

Allantoin, Panthenol

WARNING

WARNINGS: For external use only. When using this product avoid contact with eyes. If

contact with eyes occurs, flush with water.

ASK DOCTOR

Stop use and ask a doctor if irritation

develops and persists.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, seek prompt medical attention.

SAFE HANDLING WARNING

Flammable. Keep away from open flames. Do not store above 110 degrees.

QUESTIONS

Questions: 1-877-773-9800

OTHER SAFETY INFORMATION

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BZK HAND SANITIZER 
bzk hand sanitizer spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58418-187
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
WATER (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58418-187-05	15 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/01/2012
2	NDC: 58418-187-10	10 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/01/2012
3	NDC: 58418-187-01	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/01/2012
4	NDC: 58418-187-02	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/01/2012
5	NDC: 58418-187-04	120 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/01/2012
6	NDC: 58418-187-08	240 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/01/2012
7	NDC: 58418-187-17	50.275 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/01/2012
8	NDC: 58418-187-70	211200 mL in 1 DRUM; Type 0: Not a Combination Product	02/02/2020
9	NDC: 58418-187-32	1228800 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product	02/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/01/2012

Labeler - Tropical Enterprises International, Inc. (091986179)

Registrant - Tropical Enterprises International, Inc. (091986179)