FDA.reportPublic FDA data

Noble Hand

Manufacturer
BOUNCE COMPANY CO., LTD | TERAECO., LTD
Effective date
2020-05-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:13:35

Label at a glance#

ProductNoble Hand
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Dosage sectionDosage section

WARNINGS SECTION

Warning SectionWarning Section

INACTIVE INGREDIENT SECTION

Inactive sectionInactive section

INDICATIONS & USAGE SECTION

Indication sectionIndication section

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of childrenKeep out of children

OTC - PURPOSE SECTION

Purpose sectionPurpose section

OTC - ACTIVE INGREDIENT SECTION

Active IngredientActive Ingredient

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage LabelHand Clean Gel

Noble Hand

Ehtanol 70%

Cleaning with secondary water after first cleaning is better for cleaning

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
77866-001-012022-01-28C16284748780-1d6a99b39-8c33-a426-e053-dadaa90af4c2a5b38239-9e8c-ea33-e053-2995a90a08dc

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77866-001-01Noble Hand500 mL in 1 BOTTLE, PUMPGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77866-001NOBLE HAND (HAND SANITIZER) GEL [BOUNCE COMPANY CO., LTD]1Legacy NDC, 1 package rows20200519_a5b38239-9e8c-ea33-e053-2995a90a08dc.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77866-00177866-001-01

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
PROPYLENE GLYCOL6DC9Q167V3IACT
ALOE VERA LEAFZY81Z83H0XIACT
ROSEMARYIJ67X351P9IACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
CARBOMER 9404Q93RCW27EIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
TROLAMINE9O3K93S3TKIACT

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
a5b38239-9e8d-ea33-e053-2995a90a08dca5b38239-9e8c-ea33-e053-2995a90a08dc2020-05-15WarningsExact identifier
spl id: a5b38239-9e8d-ea33-e053-2995a90a08dc
spl set id: a5b38239-9e8c-ea33-e053-2995a90a08dc

Reported adverse events (FAERS/openFDA)#

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