FDA.reportPublic FDA data

Baruo Hand Sanitizer

Manufacturer
THE SUN CO.LTD
Effective date
2020-04-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:06:07

Label at a glance#

ProductBaruo Hand Sanitizer
Active ingredientAlcohol
Label structure10 sections

Indications and uses

Uses ■ Hand sanitizer to decrease bacteria on the skin that could cause disease

Dosage and administration

Directions ■ Take an appropriate amount on your hands and rub thoroughly to dry. ■ For children under 6, use only under adult supervision ■ not recommended for infants

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Ethyl alcohol 70.0 %v/v

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Water, Carbomer, Aminomethyl Propanol, Aloe Vera Gel, Butylene Glycol, Disodium EDTA, Grapefruit Seed Extract, Green Tea Extract, Phenoxyethanol

PURPOSE

OTC - PURPOSE SECTION

PURPOSE: Antiseptic

WARNINGS

WARNINGS SECTION

Warnings:


For external use only-hands

Flammable. Keep away from heat and 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 skin irritation or rash develops.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Uses

INDICATIONS & USAGE SECTION

Uses
■ Hand sanitizer to decrease bacteria on the skin that could cause disease

Directions

DOSAGE & ADMINISTRATION SECTION

Directions
■ Take an appropriate amount on your hands and rub thoroughly to dry.
■ For children under 6, use only under adult supervision
■ not recommended for infants

Other Information

OTHER SAFETY INFORMATION

Other Information
■ Read the directions and warnings before use
■ Avoid freezing and excessive heat above 40 degree C (104 degree F)
■ Storing the product in a different container may cause accidents or
deterioration of quality. Therefore, keep the product in its original container.
■ May discolor some fabrics or surfaces.

QUESTIONS

OTC - QUESTIONS SECTION

Questions
www thesunin.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74923-030-012022-01-28C16284748780-1d6a99b39-547e-a426-e053-dadaa90af4c288409f10-ac48-4890-a97e-7b4945c9eddb

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74923-030-01Baruo Hand Sanitizer500 mL in 1 BOTTLE, PUMPGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74923-030BARUO HAND SANITIZER (ALCOHOL) GEL [THE SUN CO.LTD]1Legacy NDC, 1 package rows20200414_88409f10-ac48-4890-a97e-7b4945c9eddb.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74923-03074923-030-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
Alcohol3K9958V90MACTIB
Water059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
ALOE VERA LEAFZY81Z83H0XIACT
Butylene Glycol3XUS85K0RAIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
CITRUS PARADISI SEED12F08874Y7IACT
GREEN TEA LEAFW2ZU1RY8B0IACT
PhenoxyethanolHIE492ZZ3TIACT

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
1aaa2608-a80e-44a5-b919-68d8684e510b88409f10-ac48-4890-a97e-7b4945c9eddb2020-04-14WarningsExact identifier
spl id: 1aaa2608-a80e-44a5-b919-68d8684e510b
spl set id: 88409f10-ac48-4890-a97e-7b4945c9eddb

Reported adverse events (FAERS/openFDA)#

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