FDA.reportPublic FDA data

Ariul Stress Relieving Hand Sanitizing Gel

Manufacturer
Beauty Factory Co., Ltd. | SAIMDANG Cosmetics CO.,LTD.
Effective date
2020-05-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:09:51

Label at a glance#

ProductAriul Stress Relieving Hand Sanitizing Gel
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ariul Stress Relieving Hand Sanitizing GelAriul Stress Relieving Hand Sanitizing Gel

OTC - ACTIVE INGREDIENT SECTION

DOSAGE & ADMINISTRATION SECTION

OTC - PURPOSE SECTION

INDICATIONS & USAGE SECTION

INACTIVE INGREDIENT SECTION

OTC - DO NOT USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - WHEN USING SECTION

INSTRUCTIONS FOR USE SECTION

WARNINGS SECTION

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77416-750-012021-07-23C16284748780-1c7ccaba7-12ff-fd44-e053-dadaa90aa01b[Ariul Stress Relieving Hand Sanitizing Gel] 50 ml : 77416-750-01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77416-750-01Ariul Stress Relieving Hand Sanitizing Gel50 mL in 1 TUBEGEL501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77416-750ARIUL STRESS RELIEVING HAND SANITIZING GEL (ETHYL ALCOHOL) GEL [BEAUTY FACTORY CO., LTD.]1Legacy NDC, 1 package rows20200506_a4f348d1-95a9-5cba-e053-2a95a90ac287.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77416-75077416-750-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
GREEN TEA LEAFW2ZU1RY8B0IACT
MORUS ALBA ROOTCST1G9BZGDIACT
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
TROLAMINE9O3K93S3TKIACT
ALCOHOL3K9958V90MACTIB

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
a4f25c1a-b3c9-4ade-e053-2995a90afb4fa4f348d1-95a9-5cba-e053-2a95a90ac2872020-05-05Exact identifier
spl id: a4f25c1a-b3c9-4ade-e053-2995a90afb4f
spl set id: a4f348d1-95a9-5cba-e053-2a95a90ac287

Reported adverse events (FAERS/openFDA)#

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