KAZU HAND SANITIZER WIPES by N Bridge Inc. / WOOIL C&TECH.CORP

KAZU HAND SANITIZER WIPES by

Drug Labeling and Warnings

KAZU HAND SANITIZER WIPES by is a Otc medication manufactured, distributed, or labeled by N Bridge Inc., WOOIL C&TECH.CORP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

KAZU HAND SANITIZER WIPES- alcohol cloth 
N Bridge Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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benzalkonium chloride

water, glycerin, polysorbate 80, sodium benzoate, benzalkonium chloride, citric acid, maltodextrin, aloe barbadensis leaf juice powder, limonene, tocopheryl acetate, linalool, citral, citronellol, geraniol, benzyl benzoate, benzyl salicylate, farnesol, eugenol, isoeugenol, benzyl alcohol, fragrance

Antiseptic

keep out of reach of the children

Wipe hands thoroughly with product and allow to dry.

Discard wipe in trash. Do not flush.

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

When using this product keep out of eyes. in case of contact with eyes, flush thoroughly with water.

avoid contact with broken skin.

do not inhale or ingest.

Stop use and ask a doctor if irritation and redness develop. condition persists for more than 72 hours.

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

for external use only

KAZU HAND SANITIZER WIPES 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76966-0007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1677 g

Inactive Ingredients
Ingredient Name	Strength
CITRAL (UNII: T7EU0O9VPP)
GERANIOL (UNII: L837108USY)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
FARNESOL (UNII: EB41QIU6JL)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
SODIUM BENZOATE (UNII: OJ245FE5EU)
WATER (UNII: 059QF0KO0R)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BENZYL BENZOATE (UNII: N863NB338G)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
EUGENOL (UNII: 3T8H1794QW)
ISOEUGENOL (UNII: 5M0MWY797U)
BENZYL ALCOHOL (UNII: LKG8494WBH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76966-0007-1	50 in 1 PACKAGE; Type 0: Not a Combination Product	06/15/2020	07/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/15/2020	07/30/2020

Labeler - N Bridge Inc. (694892752)

Registrant - N Bridge Inc. (694892752)

Establishment
Name	Address	ID/FEI	Business Operations
WOOIL C&TECH.CORP		688331078	manufacture(76966-0007)

Establishment
Name	Address	ID/FEI	Business Operations
N Bridge Inc.		694892752	label(76966-0007)

Revised: 7/2020

Document Id: abb6a9a3-4273-49fd-e053-2995a90ab3aa

34390-5

Set id: a8a41c19-5576-ea00-e053-2a95a90a9a40

Version: 2

Effective Time: 20200731