FDA.reportPublic FDA data

KAZU HAND SANITIZER WIPES

Manufacturer
N Bridge Inc. | WOOIL C&TECH.CORP
Effective date
2020-06-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:24:54

Label at a glance#

ProductKAZU HAND SANITIZER WIPES
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

benzalkonium chloride

INACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

Antiseptic

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Wipe hands thoroughly with product and allow to dry.

Discard wipe in trash. Do not flush.

WARNINGS SECTION

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.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76966-000776966-0007-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
CITRALT7EU0O9VPPIACT
GERANIOLL837108USYIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
FARNESOLEB41QIU6JLIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
SODIUM BENZOATEOJ245FE5EUIACT
WATER059QF0KO0RIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
GLYCERINPDC6A3C0OXIACT
POLYSORBATE 806OZP39ZG8HIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
BENZYL BENZOATEN863NB338GIACT
MALTODEXTRIN7CVR7L4A2DIACT
LIMONENE, (+)-GFD7C86Q1WIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
EUGENOL3T8H1794QWIACT
ISOEUGENOL5M0MWY797UIACT
BENZYL ALCOHOLLKG8494WBHIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
abb6a9a3-4273-49fd-e053-2995a90ab3aaa8a41c19-5576-ea00-e053-2a95a90a9a402020-07-31WarningsExact identifier
spl set id: a8a41c19-5576-ea00-e053-2a95a90a9a40

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.