KAZU BEAUTY ANTIBACTERIAL HAND SANITIZER

Manufacturer
N Bridge Inc. | WHITE COSPHARM CO.,LTD.
Effective date
2020-07-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:22:05

Label at a glance#

ProductKAZU BEAUTY ANTIBACTERIAL HAND SANITIZER
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol

INACTIVE INGREDIENT SECTION

water, carbomer, polysorbate 20, isopropyl myristate, aminomethyl propanol, disodium edta, grapefruit extract, aloe vera gel

OTC - PURPOSE SECTION

Antiseptic

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

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 SECTION

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 SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130810002332500GTIN-13: 0810002332500
EAN-13: 0810002332500
GTIN-12: 810002332500
UPC-A: 810002332500
GTIN storage (14 digits): 00810002332500
label.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76966-0010-12022-01-28C16284748780-1d6a99b39-5db8-a426-e053-dadaa90af4c2aaed1bcc-656e-5fb2-e053-2995a90aa18a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76966-0010-1KAZU BEAUTY ANTIBACTERIAL HAND SANITIZER500 mL in 1 BOTTLE, PUMPGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76966-0010KAZU BEAUTY ANTIBACTERIAL HAND SANITIZER (ALCOHOL) GEL [N BRIDGE INC.]1Legacy NDC, 1 package rows20200721_aaed1bcc-656e-5fb2-e053-2995a90aa18a.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76966-001076966-0010-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

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
aaed2286-2539-44c9-e053-2995a90a3b19aaed1bcc-656e-5fb2-e053-2995a90aa18a2020-07-21WarningsExact identifier
spl id: aaed2286-2539-44c9-e053-2995a90a3b19
spl set id: aaed1bcc-656e-5fb2-e053-2995a90aa18a

Reported adverse events (FAERS/openFDA)#

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