KAZU ANTIBACTERIAL HAND SANITIZING WIPES- benzalkonium chloride cloth

KAZU ANTIBACTERIAL HAND SANITIZING WIPES by

Drug Labeling and Warnings

KAZU ANTIBACTERIAL HAND SANITIZING WIPES by is a Otc medication manufactured, distributed, or labeled by N Bridge Inc., FIRSTCHAM CO., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

benzalkonium chloride

INACTIVE INGREDIENT

water, disodium EDTA, sodium benzoate, glycerin, polysorbate 20, tocopheryl acetate, phenoxyethanol, citric acid

PURPOSE

Antiseptic

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

wet hands thoroughly with product and allow to dry without wiping

for children under 6, use only under adult supervision

not recommended for infants

WARNINGS

For external use only. Flammable. Keep away from heat or flame.

Do not use

• in children less than 2 months of age
• on open skin wounds

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KAZU ANTIBACTERIAL HAND SANITIZING WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76966-0017
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.197 g  in 50

Inactive Ingredients
Ingredient Name	Strength
PHENOXYETHANOL (UNII: HIE492ZZ3T)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
SODIUM BENZOATE (UNII: OJ245FE5EU)
WATER (UNII: 059QF0KO0R)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76966-0017-1	50 in 1 PACKAGE; Type 0: Not a Combination Product	07/27/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/27/2020

Labeler - N Bridge Inc. (694892752)

Registrant - N Bridge Inc. (694892752)

Establishment
Name	Address	ID/FEI	Business Operations
FIRSTCHAM CO., LTD		689905446	manufacture(76966-0017)

Establishment
Name	Address	ID/FEI	Business Operations
N Bridge Inc.		694892752	label(76966-0017)