FDA.reportPublic FDA data

[WHAIN COSMETIC] TOP TOON Dr.Q Hand Sanitizer Spray 73823-202-01

Manufacturer
WHAIN COSMETIC
Effective date
2021-01-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:37:11

Label at a glance#

ProductTOP TOON Dr.Q Hand SanitizerSpray
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

TOP TOON Dr.Q Hand Sanitizer SprayTOP TOON Dr.Q Hand Sanitizer Spray

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
1041849ethanol 70 % Topical SprayPSN1
1041849ethanol 0.7 ML/ML Topical SpraySCD1
1041849ethanol 70 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73823-202-012023-01-30C16284748780-1f386c64a-2569-0266-e053-dadaa90a7c1a[WHAIN COSMETIC] TOP TOON Dr.Q Hand Sanitizer Spray 73823-202-01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73823-202-01TOP TOON Dr.Q Hand SanitizerSpray500 mL in 1 BOTTLE, SPRAYSPRAY5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73823-202TOP TOON DR.Q HAND SANITIZERSPRAY (ALCOHOL) SPRAY [WHAIN COSMETIC]1Legacy NDC, 1 package rows20210122_b95fe6ca-d224-ba28-e053-2a95a90ab628.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73823-20273823-202-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
ALCOHOL3K9958V90MACTIB
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
b95fa3d0-021c-ad98-e053-2a95a90ad5c4b95fe6ca-d224-ba28-e053-2a95a90ab6282021-01-20Exact identifier
spl id: b95fa3d0-021c-ad98-e053-2a95a90ad5c4
spl set id: b95fe6ca-d224-ba28-e053-2a95a90ab628

Reported adverse events (FAERS/openFDA)#

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