FLAWLESS HAND SANITIZER

Manufacturer
NBIO CO., LTD.
Effective date
2020-05-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:13:12

Label at a glance#

ProductFLAWLESS HAND SANITIZER
Active ingredientPROPOLIS WAX
Label structure10 sections

Indications and uses

■ Hand sanitizer to help reduce bacteria that potentially can cause disease. ■ For use when soap and water are not available.

Dosage and administration

■ Please spray it at a distance of 10~20cm so that your hands are enough covered. Rub hands together until dry. ■ Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Propolis Extract 0.5%

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Sodium Silicate

PURPOSE

OTC - PURPOSE SECTION

Sanitizer

WARNINGS

WARNINGS SECTION

■ For external use only.
--------------------------------------------------------------------------------------------------------
When using this product
■ Do not use in or near the eyes. In case of contact, rinse eyes thoroughly
with water.
■ Avoid contact with broken skin.
■ Do not inhale or ingest.
--------------------------------------------------------------------------------------------------------
Stop use and ask a doctor
■ If irritation or rash appears and lasts.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

■ If swallowed, get medical help or contact a Poison Control Center right away

Uses

INDICATIONS & USAGE SECTION

■ Hand sanitizer to help reduce bacteria that potentially can cause disease.
■ For use when soap and water are not available.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Please spray it at a distance of 10~20cm so that your hands are enough covered. Rub hands together until dry.
■ Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

OTHER SAFETY INFORMATION

■ Store between 41~86℉(Between 5~30℃)
■ Avoid freezing and excessive heat above 104℉(40℃) and direct sunlight.

QUESTIONS

OTC - QUESTIONS SECTION

■ www.nbio.kr / 82-31-432-5670

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77560-010-012024-01-30C16284748780-11030e365-2fef-111a-e063-dadaa90a10e2c39a631b-189f-4557-b678-d32277273899

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77560-010-01FLAWLESS HAND SANITIZER250 mL in 1 BOTTLE, SPRAYSPRAY2501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77560-010FLAWLESS HAND SANITIZER (PROPOLIS EXTRACT) SPRAY [NBIO CO., LTD.]1Legacy NDC, 1 package rows20200515_c39a631b-189f-4557-b678-d32277273899.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77560-01077560-010-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPOLIS WAX6Y8XYV2NOFACTIB
Water059QF0KO0RIACT
Sodium SilicateIJF18F77L3IACT

Source Document#

Source XML · Source PDF

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
5c2e492d-a8c2-43a5-8add-0076ec04b6f9c39a631b-189f-4557-b678-d322772738992020-05-15WarningsExact identifier
spl id: 5c2e492d-a8c2-43a5-8add-0076ec04b6f9
spl set id: c39a631b-189f-4557-b678-d32277273899

Reported adverse events (FAERS/openFDA)#

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