FDA.reportPublic FDA data

[Formal Bee Daily Instant Hand Sanitizer Spray] 50 ml : 74064-2050

Manufacturer
KOREA COSPACK CO.,LTD.
Effective date
2020-04-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:06:31

Label at a glance#

ProductFormal Bee Daily Instant Hand SanitizerSpray
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FORMALFORMAL

OTC - ACTIVE INGREDIENT SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - PURPOSE SECTION

WARNINGS SECTION

DOSAGE & ADMINISTRATION SECTION

INACTIVE INGREDIENT SECTION

OTC - DO NOT USE SECTION

OTHER SAFETY INFORMATION

OTC - STOP USE SECTION

OTC - ASK DOCTOR SECTION

INDICATIONS & USAGE SECTION

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020364ethanol 62 % Topical SprayPSN1
1020364ethanol 0.62 ML/ML Topical SpraySCD1
1020364ethanol 62 % Topical SpraySY1
1020364ethyl alcohol 62 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74064-2050-12021-07-23C16284748780-1c7ccaba7-2922-fd44-e053-dadaa90aa01b[Formal Bee Daily Instant Hand Sanitizer Spray] 50 ml : 74064-2050

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74064-2050-1Formal Bee Daily Instant Hand SanitizerSpray50 mL in 1 BOTTLE, SPRAYSPRAY501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74064-2050FORMAL BEE DAILY INSTANT HAND SANITIZERSPRAY (ALCOHOL) SPRAY [KOREA COSPACK CO.,LTD.]1Legacy NDC, 1 package rows20200416_a365ab05-5078-e8cc-e053-2995a90a0281.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
74064-205074064-2050-1

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
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PANTHENOLWV9CM0O67ZIACT
GLYCYRRHIZINATE DIPOTASSIUMCA2Y0FE3FXIACT
ALOE VERA LEAFZY81Z83H0XIACT
HYALURONATE SODIUMYSE9PPT4THIACT
LEMON24RS0A988OIACT
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
a365a1ec-84a3-e7df-e053-2995a90a92eea365ab05-5078-e8cc-e053-2995a90a02812020-04-15Exact identifier
spl id: a365a1ec-84a3-e7df-e053-2995a90a92ee
spl set id: a365ab05-5078-e8cc-e053-2995a90a0281

Reported adverse events (FAERS/openFDA)#

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