FDA.reportPublic FDA data

TOP TOON Dr.Q Hand Sanitizer Gel

Manufacturer
WHAIN COSMETIC
Effective date
2021-01-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:37:10

Label at a glance#

ProductTOP TOON Dr.Q Hand Sanitizer Gel
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TOP TOON Dr.Q Hand Sanitizer GelTOP TOON Dr.Q Hand Sanitizer 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
73823-201-012023-01-30C16284748780-1f386c64a-3c1d-0266-e053-dadaa90a7c1a[WHAIN COSMETIC] TOP TOON Dr.Q Hand Sanitizer Gel 73823-201-01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73823-201-01TOP TOON Dr.Q Hand Sanitizer Gel500 mL in 1 BOTTLE, PUMPGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73823-201TOP TOON DR.Q HAND SANITIZER GEL (ALCOHOL) GEL [WHAIN COSMETIC]1Legacy NDC, 1 package rows20210122_b94d666c-5ae1-4a8c-e053-2a95a90ae0da.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
73823-20173823-201-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
BUTYLENE GLYCOL3XUS85K0RAIACT
WATER059QF0KO0RIACT
ARTEMISIA PRINCEPS LEAFSY077EW02GIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
ALCOHOL3K9958V90MACTIB
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
GLYCERINPDC6A3C0OXIACT
HYALURONATE SODIUMYSE9PPT4THIACT

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
b94d8597-ce0b-deee-e053-2a95a90a9cc5b94d666c-5ae1-4a8c-e053-2a95a90ae0da2021-01-19Exact identifier
spl id: b94d8597-ce0b-deee-e053-2a95a90a9cc5
spl set id: b94d666c-5ae1-4a8c-e053-2a95a90ae0da

Reported adverse events (FAERS/openFDA)#

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