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- benzalkonium chloride 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

label

KAZU HAND SANITIZER WIPES 
benzalkonium chloride cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 76966-0013
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.1677 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 76966-0013-150 in 1 PACKAGE; Type 0: Not a Combination Product06/15/202007/30/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/15/202007/30/2020
Labeler - N Bridge Inc. (694892752)
Registrant - N Bridge Inc. (694892752)
Establishment
NameAddressID/FEIBusiness Operations
WOOIL C&TECH.CORP688331078manufacture(76966-0013)
Establishment
NameAddressID/FEIBusiness Operations
N Bridge Inc.694892752label(76966-0013)

Revised: 7/2020
 
N Bridge Inc.