FDA.reportPublic FDA data

FRESH AND MINI HAND SANITIZER

Manufacturer
KOREA COSPACK CO.,LTD.
Effective date
2020-04-11
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:05:49

Label at a glance#

ProductFRESH AND MINI HAND SANITIZER
Active ingredientALCOHOL
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5050

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

INDICATIONS & USAGE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - WHEN USING SECTION

WARNINGS SECTION

OTC - DO NOT USE SECTION

INACTIVE INGREDIENT SECTION

STORAGE AND HANDLING SECTION

INSTRUCTIONS FOR USE SECTION

STORAGE AND HANDLING SECTION

DOSAGE & ADMINISTRATION SECTION

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN3
581662ethanol 0.7 ML/ML Topical GelSCD3
581662ethanol 70 % Topical GelSY3
581662ethyl alcohol 70 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74064-7050-12021-07-23C16284748780-1c7ccaba7-218d-fd44-e053-dadaa90aa01b[SD Biotechnologies Co., Ltd.] 50 ml : 74064-7050

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74064-7050-1FRESH AND MINI HAND SANITIZER50 mL in 1 POUCHGEL503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74064-7050FRESH AND MINI HAND SANITIZER (ALCOHOL) GEL [KOREA COSPACK CO.,LTD.]3Legacy NDC, 1 package rows20200411_a2369715-3a36-b975-e053-2995a90a073c.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
74064-705074064-7050-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
HYALURONATE SODIUMYSE9PPT4THIACT
TROLAMINE9O3K93S3TKIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
PROPYLENE GLYCOL6DC9Q167V3IACT
PANTHENOLWV9CM0O67ZIACT
GLYCYRRHIZINATE DIPOTASSIUMCA2Y0FE3FXIACT
ALOE VERA LEAFZY81Z83H0XIACT

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
a300384d-1a15-a46d-e053-2a95a90a7c53a2369715-3a36-b975-e053-2995a90a073c2020-04-11Exact identifier
spl id: a300384d-1a15-a46d-e053-2a95a90a7c53
spl set id: a2369715-3a36-b975-e053-2995a90a073c

Reported adverse events (FAERS/openFDA)#

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